Impact Factor 4.137 | CiteScore 4.28
More on impact ›

Original Research ARTICLE

Front. Oncol., 19 June 2019 | https://doi.org/10.3389/fonc.2019.00534

A Novel Translational Ovine Pulmonary Adenocarcinoma Model for Human Lung Cancer

Mark E. Gray1,2*, Paul Sullivan3, Jamie R. K. Marland3, Stephen N. Greenhalgh1, James Meehan2,4, Rachael Gregson1, R. Eddie Clutton1, Chris Cousens5, David J. Griffiths5, Alan Murray3 and David Argyle1
  • 1The Royal (Dick) School of Veterinary Studies and Roslin Institute, University of Edinburgh, Easter Bush, Edinburgh, United Kingdom
  • 2Cancer Research UK Edinburgh Centre and Division of Pathology Laboratories, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom
  • 3School of Engineering, Institute for Integrated Micro and Nano Systems, Edinburgh, United Kingdom
  • 4Institute of Sensors, Signals and Systems, School of Engineering and Physical Sciences, Heriot-Watt University, Edinburgh, United Kingdom
  • 5Moredun Research Institute, Pentlands Science Park, Midlothian, United Kingdom

In vitro cell line and in vivo murine models have historically dominated pre-clinical cancer research. These models can be expensive and time consuming and lead to only a small percentage of anti-cancer drugs gaining a license for human use. Large animal models that reflect human disease have high translational value; these can be used to overcome current pre-clinical research limitations through the integration of drug development techniques with surgical procedures and anesthetic protocols, along with emerging fields such as implantable medical devices. Ovine pulmonary adenocarcinoma (OPA) is a naturally-occurring lung cancer that is caused by the jaagsiekte sheep retrovirus. The disease has similar histological classification and oncogenic pathway activation to that of human lung adenocarcinomas making it a valuable model for studying human lung cancer. Developing OPA models to include techniques used in the treatment of human lung cancer would enhance its translational potential, making it an excellent research tool in assessing cancer therapeutics. In this study we developed a novel OPA model to validate the ability of miniaturized implantable O2 and pH sensors to monitor the tumor microenvironment. Naturally-occurring pre-clinical OPA cases were obtained through an on-farm ultrasound screening programme. Sensors were implanted into OPA tumors of anesthetized sheep using a CT-guided trans-thoracic percutaneous implantation procedure. This study reports the findings from 9 sheep that received sensor implantations. Time taken from initial CT scans to the placement of a single sensor into an OPA tumor was 45 ± 5 min, with all implantations resulting in the successful delivery of sensors into tumors. Immediate post-implantation mild pneumothoraces occurred in 4 sheep, which was successfully managed in all cases. This is, to the best of our knowledge, the first description of the use of naturally-occurring OPA cases as a pre-clinical surgical model. Through the integration of techniques used in the treatment of human lung cancer patients, including ultrasound, general anesthesia, CT and surgery into the OPA model, we have demonstrated its translational potential. Although our research was tailored specifically for the implantation of sensors into lung tumors, we believe the model could also be developed for other pre-clinical applications.

Introduction

The process of developing and validating new anti-cancer agents typically follows a step-wise process from in vitro and in vivo testing through to phase I, II, and III clinical trials. It has been estimated that several hundred million dollars and up to 10 years of research is needed to take a drug from its initial concept to the completion of phase III trials (1). Pharmaceutical companies may be discouraged from developing new cancer drugs, not only due to the resources required, but also because attrition rates for new cancer therapeutics are very high. Only 5% of agents that show pre-clinical promise gain a license to be used in patients after phase III trials (2). While the use of in vitro techniques and in vivo murine models are well-established in pre-clinical cancer research, fewer large animal translational models have been described. These models show promise in overcoming current limitations in pre-clinical research by permitting the integration of drug development techniques with surgical procedures and anesthetic protocols, along with novel cancer therapeutic strategies such as implantable medical devices.

The use of implantable medical devices for cancer diagnosis, treatment, and monitoring is becoming attainable due to advances in electronics and microfabrication techniques. In vivo murine studies have already shown that implantable devices can be used to detect cancer secreted biomarkers (3) or to release chemotherapy drugs directly within tumors (4). Numerous other studies have also investigated the biocompatibility and functionality of implantable devices using in vivo (predominantly rodent) models for a range of other disease conditions, providing evidence of their increasing potential for clinical uses (5).

Lung cancer remains the most commonly diagnosed cancer in the world, with ~1.8 million new cases and 1.6 million cancer-related deaths recorded each year (6). Information on the molecular basis and pathogenesis of human lung cancer continues to grow through the use of numerous in vitro cell line and in vivo murine models (712). However, pre-clinical research using murine models has failed to improve overall survival rates, which remains low (~15%).

Comparative oncology is the use of naturally-occurring cancers that arise in veterinary species for the study of cancer biology and therapy (13); this approach is increasingly being used to reconcile the gap between in vitro experiments, in vivo small animal research and human clinical trials. Naturally-occurring tumors within veterinary species that have incidence rates or pathological similarities comparable to human cancers have considerable potential as translational models of human disease (14). Ovine pulmonary adenocarcinoma (OPA) is a naturally-occurring neoplastic lung disease caused by the jaagsiekte sheep retrovirus (JSRV) (1518). The disease is regarded as a valuable translational pre-clinical research model for studying human lung cancer, overcoming many of the limitations associated with current murine models (19).

The Implantable Microsystems for Personalized Anti-Cancer Therapy (IMPACT) programme (University of Edinburgh) is developing miniaturized implantable O2 and pH sensors designed to monitor the tissue microenvironment within a solid tumor. The identification of hypoxic tumor regions should improve the ability to target these radiation and chemo-resistant areas (20). Each sensor is fabricated on a silicon chip and bonded to a 1.7 × 200 mm long flexible printed circuit board lead. The sensors are sealed in biocompatible epoxy resin, resulting in an overall sensor size of ~2.8 × 5.1 × 1.4 mm (width × length × height). The sensors are sterilized using ethylene oxide. We have capitalized upon a naturally-occurring OPA model in order to validate these sensors within a solid tumor. By integrating techniques used in the treatment of human lung cancer patients (ultrasound, general anesthesia, CT, and surgery) into the OPA model, we have shown its translational potential. Whilst our model was specifically developed for the implantation of sensors into solid tumors, we believe it has considerable potential for other pre-clinical studies.

Materials and Methods

Studies were undertaken under a UK Home Office Project License in accordance with the Animals (Scientific Procedures) Act 1986 and with approval from the University of Edinburgh Animal Welfare and Ethical Review Boards. The recommended guidelines for welfare and use of animals in research were followed. Nine adult female sheep (Highlander, n = 1; Scottish blackface, n = 7; Scotch Mule, n = 1), weighing 39–65 kg and diagnosed with naturally-occurring pre-clinical OPA, were obtained through an on-farm ultrasound eradication programme (21, 22). Sheep were bedded on straw, with ad libitum access to food and water in groups of at least 2 animals and were allowed a period of adaptation of at least 24 h before undergoing anesthesia.

General Anesthesia

Anesthesia was managed by specialist veterinary anesthetists or by veterinary surgeons enrolled in a specialist training programme under supervision. All sheep underwent preanaesthetic assessment, which involved distant observation of demeanor, breathing rate and pattern, and was followed by physical examination. Only animals that were judged fit for anesthesia were subsequently studied. Food was withheld for 12 h before anesthesia, but access to water was permitted until preanaesthetic medication was administered. Anesthesia and analgesia techniques are provided in Table 1. Intravenous preanaesthetic medication was administered to reduce animal stress, facilitate the induction of anesthesia and to decrease induction agent dose requirements. General anesthesia was induced within 10 min of preanaesthetic medication to minimize sedation-induced respiratory depression. Before this, and when necessary, the head was elevated to prevent respiratory secretions and rumen contents entering the upper airway. After induction of anesthesia, the trachea was intubated with a cuffed endotracheal tube and the cuff inflated. Anesthesia was maintained using isoflurane (Abbot Animal Health, Maidenhead, UK) vaporized in an O2/air mixture, administered using a Bain or circle breathing system connected to the endotracheal tube. End-tidal concentrations of 1.5–2.0% isoflurane were used to ensure unresponsiveness to subsequent procedures. Oropharyngeal and tracheobronchial suction was performed to remove respiratory secretions when required. After tracheal intubation, the lungs were ventilated mechanically to achieve tidal volumes of 8–10 ml/kg. Respiratory rate was adjusted to maintain normocapnia (PaCO2 range 4.7–6 kPa). Body temperature was monitored using rectal and esophageal thermistors and maintained between 38.5°C and 39.5°C. A central (jugular) venous 14G cannula was used for administering drugs and crystalloid fluids. Compound sodium lactate (Aqupharm No 11, Animalcare, York, UK) was infused at 5/ml/kg/h in order to sustain cardiac preload and replace lost fluids and electrolytes. Mean arterial blood pressure was maintained between 70 and 80 mmHg and monitored using an arterial cannula placed in the central auricular artery. Blood samples obtained from the arterial cannula was used for intermittent blood-gas, biochemical and hematological analysis (Epoc portable blood gas electrolyte and critical care analyser; Woodley Equipment Company Ltd, Lancashire, UK). A multiparameter patient monitoring device (Datex-Ohmeda S/5, SOMA Technology, Madison, USA) was used to continuously monitor pulse rate and blood pressure along with pulse oximetry, capnography, temperature, spirometry, electrocardiography and inspired and expired gases (O2, CO2, and inhalant anesthetic agent) (Figure 1). Analgesic agents were administered pre-emptively either at the time of sedation or immediately post-induction. All animals were euthanized with intravenous sodium pentobarbitone (Pentoject; Animalcare, York, UK).

TABLE 1
www.frontiersin.org

Table 1. Techniques used to provide anesthesia and analgesia in sheep with ovine pulmonary adenocarcinoma in pre-clinical research.

FIGURE 1
www.frontiersin.org

Figure 1. Photographs of imaging and surgical facilities. (a) The sheep is anesthetized and positioned for CT scanning in lateral recumbency, with the OPA affected lungs uppermost. The anesthetic monitoring equipment can be seen to the left-hand side of the image. (b) For sensor implantation a general surgical kit is required along with the Jamshidi insertion needle. An IMPACT sensor can be seen in a bottle of sterile saline at the top right-hand side of the image. (c) Macroscopic image of the IMPACT O2 sensor encapsulated in a biocompatible epoxy resin and bonded to the lead wire.

Computed Tomography Imaging

A single-section SOMATOM Definition AS 64 slice helical CT machine (Siemens Healthcare Ltd, Camberley, UK) was used for all advanced imaging procedures. The imaging parameters of the scanner were 120 kVp, 35 mA, 3–5 mm collimation with 1 mm section thickness. The window width and level were ~2,000 and −500 HU, respectively, allowing simultaneous visualization of the needle tip, blood vessels, OPA lesions, pneumothorax, bone, muscle, and fat. All scans were performed to include the entire thoracic cavity from the thoracic inlet to the last rib.

Development of a Trans-Thoracic Percutaneous Technique for Sensor Implantation Into OPA Tumors

The model was initially developed using cadavers of OPA-affected sheep; simulated surgeries were performed on 8 sheep cadavers with multiple sensor implantations in each carcass. These surgeries allowed the development of the implantation procedure and investigation of the potential accessible regions of the thoracic cavity and lung lobes into which sensors could be safely implanted. To refine the surgical procedure further, 3 sheep diagnosed with pre-clinical OPA by ultrasound screening underwent anesthesia and sensor implantation as developed from the cadaveric studies. Refinements to the procedure included the use of radiopaque grid lines for improved accuracy of lesion localization and performing serial CT scans to aid needle positioning and sensor implantation. These staged series of experiments allowed the development of our OPA model; each development stage increased the complexity of the model, resulting in the refined protocol used in experimental cases.

All experiments were conducted on anesthetized animals. After induction of anesthesia, sheep were placed in lateral recumbency with the diseased lung uppermost. The thorax was clipped between the caudal border of the last rib and the caudal border of the scapula. The dorsal margin extended from the dorsal spinous process of the thoracic vertebrae ventrally to the sternum. An initial CT scan was taken to assess intra-thoracic pathology and identify OPA lesions for implantation. Lesions were selected so the needle path would avoid bullae, fissures, visible blood vessels, and large bronchioles. Peripheral lung lobe lesions of at least 4 cm diameter were preferred to limit the volume of normal aerated lung that the needle would pass through and to improve sensor implantation into OPA tissue (Figure 2). To aid OPA lesion localization and determine the site for percutaneous sensor placement, initial CT scans were performed with a self-adhesive sheet of non-metallic, radiopaque grid lines (GuideLines, Oncology Imaging Systems, UK) placed on the thoracic wall skin surface. OPA lesions were localized dorso-ventrally based on the grid lines and cranio-caudally based on intercostal spaces. The distance between the skin and pleura was measured at the anticipated penetration site. A mark was drawn on the skin surface to identify the position of thoracic wall penetration for sensor implantation. The grid lines were removed, and the skin was aseptically prepared for surgery using chlorohexidine solution, after which the area was four quarter draped for surgery (Figure 3).

FIGURE 2
www.frontiersin.org

Figure 2. Initial CT images are used to assess intra-thoracic pathology. (a) Axial, (b) Coronal, and (c) Sagittal planes. A large area of increased radiopacity, consistent with an OPA lesion, can be seen affecting the ventral regions of the left cranial and caudal lung lobes (outlined in black). Air bronchograms are visible within this region (white arrows). An area of patchy and hazy increased opacity (ground glass appearance) within the dorsal regions of the lung, with preservation of bronchial and vascular patterns, can also be identified (outlined in white); this increased opacity may due to the presence of diffuse areas of neoplastic foci or pneumonia. The radiopaque circles on the skin surface seen on the axial plane are the grid lines used for OPA lesion localization.

FIGURE 3
www.frontiersin.org

Figure 3. OPA lesion localization. The hemithorax has been clipped for surgery and the radiopaque grid lines are placed on the skin surface. (a) The grid lines are placed on the skin surface prior to the initial CT scan. (b,c) The skin is marked both dorso-ventrally and cranio-caudally at the desired implantation point based on the initial CT images.

All sensors were inserted using a trans-thoracic percutaneous technique under CT guidance. Based on the initial pre-operative CT scan a 1 cm vertical skin incision was made ~1–2 intercostal spaces caudal to the desired entry point into the thoracic cavity. An 8G ×15 cm Jamshidi biopsy needle (Carefusion, France), with its stylet in place, was advanced cranially through subcutaneous tissues, then redirected perpendicular to the thoracic wall in the center of the chosen intercostal space. The needle was advanced through the chest wall (based on the pre-measured distance from the initial CT scan), with the penetration of the parietal pleura appreciated as the feeling of a “pop.” The needle, at this point, was within the thoracic cavity through the parietal pleura, but not penetrating lung/OPA tissue. A second CT scan at this stage confirmed the position of the needle. If necessary, the needle could be repositioned with minimal risk of lung damage as the needle had not penetrated the visceral pleura. Once in the correct position the needle was slowly advanced through the visceral pleura into OPA tissue; repeat CT scans were taken following each needle advancement and measurements were made determining the distance from needle tip to the point of desired sensor implantation. Following placement of the needle tip centrally within OPA tissue, the stylet was removed from the Jamshidi needle and the sensor and lead wire were introduced down the bore of the needle. The obturator was then placed down the bore of the needle, advancing the sensor past the tip of the needle into OPA tissue. Once in place, the obturator and implantation needle were withdrawn, leaving the sensor and lead wire in situ. A purse string suture of 3 metric braided silk (Mersilk, Ethicon UK), placed around the incision which continued as a Chinese finger trap suture around the lead wire, secured the sensor in place (Figures 4, 5). Final CT scans were performed to evaluate sensor positioning and assess any immediate post-operative complications such as pneumothorax or hemorrhage. The decision to drain any pneumothorax that developed (though percutaneous thoracocentesis) was made based on its severity. Post-mortem examination was performed following the completion of the experiments to assess the extent of lung pathology, identify the implant site and to obtain biopsy specimens for histopathology.

FIGURE 4
www.frontiersin.org

Figure 4. Intra-operative photographs depicting trans-thoracic percutaneous sensor placement. (a,b) A skin incision is made through which the Jamshidi needle is introduced. (c–e) Following successive CT scans the needle is progressively advanced into OPA tissue. (f–h) Once the needle is in position the stylet is removed and the sensor introduced down the bore of the needle. (i) The obturator is used to push the sensor past the tip of the needle into OPA tissue. (j–l) The Jamshidi needle is removed, leaving the sensor and lead wire in place. (m–o) The skin is closed, and lead wire secured in place with a purse string and Chinese finger trap suture.

FIGURE 5
www.frontiersin.org

Figure 5. Serial CT images taken during sensor implantation. Coronal, axial, and sagittal planes are viewed following initial needle placement and after each needle advancement. The Jamshidi needle (yellow arrows) is advanced until the tip is positioned at the desired point within the OPA lesion. CT images taken immediately post-implantation demonstrates sensor placement within OPA tissue in all 3 planes (red arrows).

Histopathology

OPA tissue was fixed for at least 24 h (depending on tissue thickness) in 4% formaldehyde (Genta Medical, UK) before undergoing processing using the Thermo Scientific Excelsior AS Tissue Processor (Thermo Scientific, UK) and embedding in paraffin. Tissue was sectioned using the Leica RM2235 rotary microtome (Leica Microsystems Ltd, UK); microtome sections of 4 μm were placed on SuperFrost Plus glass slides (Thermo Scientific, UK) and allowed to dry for a minimum of 4 h at 53°C.

For haematoxylin and eosin staining, sections were deparaffinised by 3 changes in 100% xylene for 5 min, then rehydrated by placing into alcohol; 2 changes in 100% ethanol, followed by 80% then 50% for 2 min each time. The slides were washed in running water for 2 min, before placing in haematoxylin (Shandon Harris Haematoxylin, Thermo Scientific, UK) for a maximum of 10 min. Slides were washed in running water for 2 min and then placed into Scott's tap water substitute for a maximum of 10 min until the tissue sections turned blue. Sections were counterstained by placing them into Eosin Y (Shandon Eosin Y Cytoplasmic Counterstain, Thermo Scientific, UK) for 5 min. The slides were dehydrated by placing them into alcohol; 50% ethanol for 30 s, 80% ethanol for 30 s, then 2 changes in 100% ethanol for 2 min. The slides were placed in xylene for 10 min before being mounted with coverslips using DXP mountant (Sigma-Aldrich, UK).

Assessment of Radiation Exposure During CT-Guided Sensor Implantations

To assess the amount of radiation that sheep were exposed to during CT-guided sensor implantations, the total number of CT imaging events (topograms or full thoracic scans) were recorded and individual imaging event and total dose length products (DLP) were calculated for each sheep. Individual event DLP is calculated from the CT dose index volume (CTDIvol), which is in turn based on the radiation received inside a phantom from a single rotation of the scanner, this value is then multiplied by the scan length. Total DLP for each sheep was calculated from the sum of all individual DLP's. DLP is proportional to the effective dose received by a patient and is used, in combination with CTDI, to compare scanning protocols and establish diagnostic reference levels (23).

Statistical Analysis

Data for blood-gas, biochemical and hematological analysis was analyzed with parametric tests. One-way ANOVA with Holm-Šídák multiple comparisons test were used to test for differences over time; p-values < 0.05 were deemed statistically significant. Data are shown as mean ± SEM, with all statistical analysis and graphs generated using Prism 7 (GraphPad Software, San Diego, CA, USA).

Results

Appropriate Anesthetic Protocols Enable OPA Sheep to Remain Physiologically Stable Throughout Anesthesia

To assess the physiological stability of OPA-affected sheep throughout anesthesia, data from blood-gas, biochemical, and hematological analysis was combined with variables such as heart rate, respiratory rate, body temperature, and mean arterial blood pressure. Results from sheep maintained with an inspired fraction of O2 (FIO2) of 1.0 are shown in Figure 6 (n = 3–5 per time point). The remaining 4 cases in this study were subjected to alterations in FIO2 for sensor validation experiments and are therefore not included in this analysis. Results showed that physiological and arterial blood variables remained stable throughout anesthesia. No statistically significant changes over time were identified in any measured variable (Figure 6).

FIGURE 6
www.frontiersin.org

Figure 6. (A–J) Physiological parameters and arterial blood biochemical and hematological analysis. Physiological data obtained from OPA cases maintained at FIO2 of 1.0 throughout anesthesia (one-way ANOVA with Holm-Šídák multiple comparisons test; data expressed as mean ± SEM, n = 3–5 per time point; times indicate min post-induction of anesthesia) (PaO2, arterial O2 partial pressure; PaCO2, arterial CO2 partial pressure; SaO2, hemoglobin O2 saturation; Hb, hemoglobin; PIP, peak inspiratory pressure; RR, respiratory rate; MAP, Mean arterial blood pressure; HR, heart rate; ABE, arterial base excess; HCO3-, bicarbonate; CT, core temperature).

Elevated blood lactate persisted throughout anesthesia but showed a tendency to reduce at later time points (Figure 6A). Blood pH, base excess and bicarbonate showed a similar, but opposite response (Figures 6F,G). Arterial O2 partial pressure (PaO2) showed marked individual variation (Figure 6B) and was consistently lower than expected given the FIO2 of 1.0, suggesting a compromise in the degree of O2 uptake by the alveoli. Despite this, it was possible to maintain a hemoglobin O2 saturation (SaO2) of ≥ 95% (Figure 6C). Peak inspiratory pressure increased throughout anesthesia (Figure 6D), with mean peak inspiratory pressures at 180 min almost 1.5 times greater than that recorded at 30 min. Airway suction was frequently required to clear respiratory secretions. To support mean arterial blood pressure (Figure 6E), 3 sheep required management with intravenous fluids or vasopressors. Additional treatments administered during anesthesia included atropine (1 sheep; severe bradycardia), sodium bicarbonate (1 sheep; acidosis), and glucose (1 sheep; hypoglycaemia).

CT-Guided Trans-thoracic Percutaneous Sensor Implantation Resulted in a High Success Rate of Delivery of Sensors Into OPA Lesions

A total of 9 sheep underwent general anesthesia and sensor implantation (2 additional cases were excluded from analysis due to a lack of histological evidence of OPA following post-mortem examination). Of the 9 OPA-affected sheep that underwent CT-guided sensor implantations into tumor tissue, 7 cases received a single sensor implantation and 2 cases received 2 sensors implanted into a single large OPA lesion. In the case of single sensor implantations, time taken from the initial CT scan to sensor placement was 45 ± 5 min (mean ± SEM). Double implantations took a little longer, with implant times of 50 and 73 min for each case. The number of sequential CT scans and needle advancements required from the initial needle placement to obtaining the desired position within OPA tissue ranged from 3 to 5, with 4 advancements required in 9 of the 11 sensor implantations. All implantation procedures resulted in sensor placement within OPA tissue (Figure 7). No immediate complications were identified in 5 of the cases (Table 2). Estimates of the amount of radiation received by each sheep undergoing CT-guided sensor implantation were calculated. DLPs for individual topograms and full thoracic scans were 9 ± 0.3 mGy cm and 392 ± 11 mGy cm, respectively (mean ± SEM), whereas total DLP for each sheep was 2,856 ± 392 mGy cm (mean ± SEM).

FIGURE 7
www.frontiersin.org

Figure 7. CT images taken immediately post-sensor implantation. Images (a–c) are from 3 separate OPA cases. The sensor and lead wire (red arrows) can be seen within the area of increased radiopacity, consistent with a large OPA tumor.

TABLE 2
www.frontiersin.org

Table 2. Details of OPA cases used and implantation results.

Iatrogenic Pneumothorax Is a Potential Complication Following Percutaneous Sensor Implantation

Sensor implantation in 4 cases immediately resulted in mild pneumothoraces; however, only 2 of these cases required treatment with percutaneous thoracocentesis. CT scans post-thoracocentesis confirmed lung lobe re-expansion and removal of most of the air from within the thoracic cavity. Sensor positioning was not affected by the occurrence of a pneumothorax and the sensor remained within the OPA lesion post-thoracocentesis (Figure 8).

FIGURE 8
www.frontiersin.org

Figure 8. CT images documenting iatrogenic pneumothorax. The OPA target lesion is seen as a patchy area of increased radiopacity affecting the ventral region of the left caudal lung lobe. CT scans were taken immediately post-sensor implantation and following thoracocentesis. A mild pneumothorax (outlined in blue) was evident immediately post-sensor implantation, predominately localized to the region of the implantation site. The sensor can be seen within OPA tissue (red arrows). Thoracocentesis was performed immediately post-sensor placement, which resulted in lung lobe re-expansion and removal of most of the air from within the thoracic cavity; however, a small pneumothorax at the dorsal aspect of the thoracic cavity was still evident (outlined in blue).

All Implantation Sites Were Identified During Post-mortem Examination

All sheep underwent post-mortem examination following euthanasia. Gross pathology allowed assessment of lung pathology, identification of the implant site, and provided the opportunity to obtain biopsy specimens for histological analysis. Gross pathology identified lesions that were in accordance with those identified on the CT scans in terms of number of lesions, location, and size. All sensor implantation sites were successfully identified with an entry site seen in the visceral pleura directly overlying OPA tissue. In 1 case an area of petechial hemorrhage was evident to the lung surface in the region of the implantation site; however, the remaining cases had no gross evidence of parenchymal hemorrhage or haemothorax (Figure 9). Following examination of gross pathology, the implant site was dissected from the OPA tissue. The biopsy specimen was used for both OPA diagnosis and to assess the effects of the implantation procedure on OPA/lung tissue. Histological examination confirmed OPA diagnosis in all 9 cases (the 2 excluded cases were reported as lung consolidation with marked pleural fibrosis and pleuritis). Evidence of hemorrhage within the needle tract and erythrocytes present within tumor tissue immediately adjacent to the implant site were identified in all cases (Figure 10).

FIGURE 9
www.frontiersin.org

Figure 9. Photographs depicting gross pathology seen in typical OPA cases. Each implantation site is highlighted with a black arrow. (a) Large gray consolidated mass affecting the majority of the left caudal lung lobe. An area of petechial hemorrhage can be seen on the surface of the lung surrounding the needle entry point. (b) Large gray consolidated mass affecting the majority of the left cranial lung lobe. Fibrous tissue can be seen adherent to the lung surface just cranial and ventral to the needle entry point. (c) One large dark colored mass affecting the right cranial lung lobe containing the implant site, with a further focal lesion within the left caudal lung lobe.

FIGURE 10
www.frontiersin.org

Figure 10. Histological appearance of OPA sensor implantation site. All images are haematoxylin and eosin stained sections. OPA tissue including the implantation site was obtained during the post-mortem examination. The top image shows the needle tract penetrating through the visceral pleura (right-hand side of image) and into the OPA tissue. Large numbers of erythrocytes can be seen within the needle tract. Higher magnification images document erythrocytes extending up to 250 μm from the implant site, predominately within stromal tissue.

Discussion

Similarities between OPA and human lung adenocarcinomas in terms of disease presentation, progression, and histological classification has led to the recognition of OPA as an excellent model for studying human lung cancer biology (24). In vitro (2529) and in vivo (3035) OPA experimental models are well-documented and have been successfully used to identify molecular pathways involved in lung cancer pathogenesis. However, for OPA to be used as a translational pre-clinical research model for human lung cancer, techniques used in the diagnosis and treatment of human patients must be incorporated into the model. In order to achieve this aim, protocols currently used in human thoracic medicine were incorporated into our novel OPA model, which was used for validation of the sensors which have been developed as part of this project (20).

Although certain thoracic procedures in human medicine are commonly performed under local anesthesia, general anesthesia was mandatory in our OPA model to ensure animal and personnel safety. It is therefore important to consider the general anesthetic requirements of these sheep if they are to be used in translational research. General anesthesia of sheep with OPA can be challenging but is entirely feasible if facilities and expertise are in place to provide, if required, respiratory, and cardiovascular support. These animals have variable amounts of respiratory compromise resulting from the OPA lesion(s), lung lobe consolidation, increased respiratory tract secretions, secondary infections, and anesthesia-induced atelectasis. All these factors will hinder the effective movement of inspired O2 into the blood, leading to lower PaO2 levels. Adequate blood O2 content in our cases was maintained by increasing the inspired fraction of O2 in combination with mechanical ventilation. The use of elevated peak inspiratory pressures in our cases was well-tolerated and was necessary to achieve adequate ventilation due to reduced compliance of the diseased lungs. The sheep in our study also had elevated blood lactate levels, which could have been caused by global tissue hypoxia; however, as neoplasia itself can elevate blood lactate levels (36) it is difficult to know its specific underlying etiology. The decrease in lactate levels that occurred throughout anesthesia may have been due to the provision of intravenous fluid therapy and mechanical ventilation which contribute to improved tissue O2 delivery. Although we have shown that OPA cases may require additional anesthetic monitoring with respiratory and cardiovascular support, all our cases were successfully managed throughout sensor validation experiments. These results provide evidence that OPA cases, even with relatively large tumors (as was seen with a number of our cases), can be used in procedures that require general anesthesia. Although, it should be noted that these were pre-clinical OPA cases identified by ultrasound screening and sheep showing clinical signs of OPA were specifically excluded from the study.

Lung cancer diagnosis in human patients is performed through immunohistochemistry using aspirates or biopsy samples taken using a flexible bronchoscope (37), or via a minimally-invasive trans-thoracic approach (3840). The choice of which technique to use is dependent on the location of the lesion. Central lesions involving a bronchus will be readily assessible with a bronchoscope, whereas peripheral lesions that are either not visible on endobronchial examination (41), <3 cm in diameter or those that do not show a bronchus entering the lesion on CT images will be more suited to minimally invasive trans-thoracic needle biopsy (TTNB) (38, 39, 42). Both endoscopic and percutaneous biopsy techniques could have been modified for use in our OPA model; however, for several reasons the trans-thoracic percutaneous approach was chosen. Naturally-occurring JSRV infection and transformation will typically result in OPA lesions forming initially at peripheral lung lobe regions. It is only as neoplastic foci enlarge and coalesce that central lobe regions become affected. Although tumor tissue will frequently involve bronchioles, larger bronchi may remain largely unaffected. Although endoscopy can be routinely performed in sheep (43), successful endoscopic sensor implantation would only be possible in tumors which involved bronchi of sufficient diameter that could accommodate an endoscope. This specific set of selection criteria would limit the number of cases that could be used, and logistically could only be assessed once a sheep is anesthetized and CT images have been obtained. As OPA tumors can be associated with significant volumes of lung fluid production, present in the large and small airways, this would hamper endoscopic airway visualization and make sensor implantation extremely challenging. The sensor for which we developed the model is currently wired therefore endoscopic implantation would require the lead wire to run up through the large airways and out through the larynx to be connected to external instrumentation; the presence of the endotracheal tube would make this almost impossible. These limitations associated with endoscopic sensor delivery led us to develop the minimally invasive trans-thoracic percutaneous approach for sensor implantation.

In human medicine TTNB requires the use of image guidance. Fluoroscopy, once the preferred imaging choice, enables needle advancements to be visualized in real-time (44); however, the technique has become less popular as it is not compatible with accessing deep lesions and the avoidance of vascular structures and bullae (45). Image guidance using ultrasound enables needle movements to be monitored precisely and quickly during the TTNB (46, 47); however, its use is restricted to peripheral lesions that produce an acoustic window. CT is currently the most commonly used image guidance technique for TTNB (4850). Unlike fluoroscopy, CT allows accurate planning of needle path trajectories that avoid aerated lung, bullae, fissures, and blood vessels. The procedure can also be used to sample central lesions, lesions <1 cm in diameter (51) and, similar to ultrasound, can distinguish between necrotic and solid regions of a lesion, allowing for more accurate needle positioning and better diagnostic samples to be obtained. CT can be combined with fluoroscopy (CTF) to allow needle adjustments to be made in almost real-time. The technique is primarily used for very small lesions located in difficult to access thoracic regions (costodiaphragmatic recess, near to the mediastinum or critical at-risk structures) and can be performed quickly, which is advantageous in un-cooperative or high-risk patients (52). Although any of these image techniques can be integrated for use within the OPA model, CT was chosen in our study for several reasons. CTF was not considered necessary as sheep were selected for use in our experiments on the basis that they had reasonably large OPA lesions in relatively accessible lung regions. CTF would also have required the use of lead aprons and radiation shields for safety purposes. Although ultrasound guidance could have been used for sensor implantations into OPA lesions affecting pleural surfaces, the technique could not provide an assessment of pathological lesions occurring throughout the entire thorax, and thus cannot be used to aid the selection of the most appropriate lesion for implantation. These factors directed us to use CT guidance for sensor implantations.

Serial CT scans were performed during the implantation procedure, with each CT scan reviewed at each stage of the process. The initial CT scan was used to select the OPA lesion to undergo sensor implantation, while sequential scans were used to assess needle trajectory and position. Lesion selection and needle path planning was based on known risk factors associated with the development of TTNB complications in human patients, predominantly pneumothorax and hemorrhage. Small lesions and the presence of emphysema (53) or chronic obstructive pulmonary disease (54) can increase complication rates. Although it is possible that these diseases can occur with OPA, we did not see any evidence of them based on CT imaging; therefore, their association with complications seen in the OPA model is likely to be low. Technical factors associated with performing TTNB are also known to influence the occurrence of post-operative complications, these factors are likely to have played a more significant role in the complication rate seen in our model. Technical factors that can increase the risk of TTNB complications include increased amounts of normal aerated lung crossed by the needle (55, 56), a small oblique needle angle with the thoracic pleura (57), repositioning the needle multiple times (58), a greater number of sampling procedures (59), the absence of previous ipsilateral surgery (60), using a trans-fissure approach (56) and damage to thoracic vasculature. In accordance with these known risk factors, lesions were chosen so that the needle path avoided passing through bullae, large blood vessels, bronchi and interlobar fissures. If more than one lesion was present, a peripheral lesion was chosen to decrease the amount of lung tissue that would be traversed (61). It is interesting to note that procedural length or needle dwell time within the lung is not associated with increased risk of pneumothorax (59). In our model single sensor implantations were performed in a time of 45 ± 5 min (mean ± SEM), similar to studies in human patients that document CT-guided TTNB times of up to 66 min (59).

In human medicine, monitoring and standardization of radiation dose from diagnostic and interventional procedures is now commonly performed in an effort to minimize potential risks to patients from radiation exposure (23). In our model the mean DLP for a single full thoracic scan was 392 ± 11 mGy cm (mean ± SEM), which is comparable with recommended diagnostic reference levels of 517 mGy cm used for human thoracic CT scans (62). As previously described, multiple CT scans were performed during sensor implantations, which resulted in a total mean DLP of 2,865 ± 392 mGy cm (mean ± SEM). This value is higher than that reported in the human literature for patients undergoing CT-guided TTNB, with one study documenting a total mean DLP of 801 mGy cm (63). However, in the same study DLPs as high as 3,684 mGy cm were reported for patients undergoing thoracic drainage procedures. The relatively high total DLPs observed in our study was due to the need to obtain high quality images for accurate needle path planning and sensor placement, which in combination with additional post-sensor implantation scans, will have increased the total radiation dose received by each sheep. However, as our results have shown that single thoracic scans were lower than human recommended diagnostic reference levels and reports for patients undergoing thoracic drainage, this provides evidence that CT-guided techniques in sheep are comparable with similar human procedures.

Following the implantation procedure, a CT scan was performed to assess for complications and to evaluate final sensor positioning. Although numerous TTNB associated complications have been documented which include infection, air embolism, lung lobe torsion, and needle tract metastasis, by far the most common complications are pneumothorax and hemorrhage (64).

Although pneumothorax rates as high as 54% have been documented (65, 66), accepted occurrence rates are more likely to be in the region 17–26%, of which ~14% will require percutaneous aspiration or chest tube insertion (57, 60, 67, 68). In our series of experiments, 4 out of 9 cases (44%) developed a mild immediate post-implantation pneumothorax, however only 2 required percutaneous needle thoracocentesis. The cases that received thoracocentesis resulted in lung lobe expansion, with the sensor remaining within the OPA lesion. In each case the pneumothorax did not reoccur; this was likely due to the removal of excess pleural air from around the implant site, allowing apposition of visceral and parietal pleural surfaces. Measures that were used to reduce the risk of pneumothorax included the use of a coaxial needle, to allow the sensor to be placed with a single pleural puncture, and careful needle path planning.

Although hemorrhage is the second most common TTNB complication that occurs in ~4–10% of cases (67, 69), the development of a haemothorax is <1% (64). Bleeding may be identified through blood coming up through the bore of the needle, or as a ground-glass appearance on CT images typically in the region of the biopsy or along the needle path. Measures that were used to reduce the risk of hemorrhage included the avoidance of large pulmonary and cardiovascular vessels. Placing the needle through the center of the intercostal space also reduced the risk of damage to intercostal neurovascular bundles. In our study no cases were identified as having post-implantation hemorrhage based on CT image evaluation; however, following post-mortem examination and implant site histopathology erythrocytes were identified within the needle tract in all cases. This finding is not unexpected as tumor tissue can have an extensive blood supply. Passage of a large needle through tumor parenchyma will inevitably damage intra-tumoural macro and microvessels. This situation is also likely to occur in human patients undergoing TTNB, but as the needle tract itself would never be biopsied there is no available data to support this. Limited amounts of erythrocytes were identified in OPA tissue away from the needle tract itself. It is possible that the OPA tissue immediately adjacent to the implant site and needle tract has reduced compliance compared with normal lung tissue, and could potentially act as a tamponade, preventing the escape of erythrocytes into the tumor tissue. The under reporting of alveolar hemorrhage based on the CT images is likely due to the appearance of the OPA lesions themselves. All cases had large OPA lesions involving the visceral pleura that were characterized as having increased radiopacity, frequently with the presence of air bronchograms. This CT appearance of typical OPA tumors would have likely obscured any hemorrhage that occurred within the needle tract itself.

The large needle size required for sensor implantation probably contributed to the complication rate encountered in the model. The needle diameter had to exceed that of the IMPACT sensor and lead wire. Consequently, an 8G Jamshidi needle was selected, which is considerably larger than the 18–22G needles that would be routinely used in human TTNB procedures. Ongoing development and miniaturization of the sensors will allow smaller diameter needles to be used. Although smaller diameter needles may reduce the occurrence of complications, our current model has shown a comparable complication rate to that seen in human patients undergoing TTNB.

Although not considered within this article, the primary aim of developing this novel OPA model was to validate the in vivo functionality of the IMPACT O2 and pH sensors within a tumor microenvironment. In order to achieve this goal, we performed a series of physiological challenges following sensor implantation. These challenges included altering blood oxygenation levels through FIO2 manipulations and varying blood pH levels though administering inhaled CO2 and altering ventilation rates. The results of sensor validation experiments will be published in separate articles and will highlight the ability of the OPA model to be used to validate novel medical technologies.

Conclusion

This paper has described the use of naturally-occurring pre-clinical OPA cases in the development of a novel in vivo ovine model for the CT-guided trans-thoracic percutaneous implantation of sensors into OPA tumors. This is, to the best of our knowledge, the first description of the use of naturally-occurring OPA cases as a surgical model. Through the integration of techniques such as ultrasound, general anesthesia, CT and surgery into the OPA model, we have demonstrated its translational potential and effectiveness as a pre-clinical research tool for human lung cancer. We have also shown our model to be comparable to TTNB in human patients in terms of procedure duration, radiation exposure, and complication rate. We believe this model can be developed further for other pre-clinical uses, such as the procurement of biopsy specimens, the development of medical devices for the local delivery of chemotherapeutic agents, monitoring the tumor microenvironment and in the assessment of the effectiveness of RT or systemic chemotherapeutic agents. This model has great potential to not only advance the molecular understanding of human lung cancer, but to also improve pre-clinical research and enhance the treatment of human lung cancer patients.

Data Availability

All datasets generated for this study are included in the manuscript.

Ethics Statement

Studies were undertaken under a UK Home Office Project License in accordance with the Animals (Scientific Procedures) Act 1986 and with approval from the University of Edinburgh Animal Welfare and Ethical Review Boards. The recommended guidelines for welfare and use of animals in research were followed.

Author Contributions

DA and AM secured funding for this research and conceptualized the initial work. MG with contributions from PS developed the surgical procedure. SG, RC, and RG conducted all anesthetic procedures. JRKM performed all engineering work. MG wrote the majority of the manuscript and composed the figures, with contributions from JM and SG who wrote parts of the introduction and anesthesia sections respectively. CC and DG were involved with obtaining pre-clinical OPA cases. Critical revisions were made by all authors. All authors read and approved the final manuscript.

Funding

This work was supported by funding from the UK Engineering and Physical Sciences Research Council, through the IMPACT programme grant (EP/K-34510/1), a Wellcome Trust Biomedical Resource Grant to the Wellcome Trust Critical Care Laboratory for Large Animals (104972/Z/14/Z) and the Scottish Government Rural and Environment Science and Analytical Services Division (RESAS).

Conflict of Interest Statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be viewed as a potential conflict of interest.

Acknowledgments

CT imaging was performed by Mrs. L. Grant (The Royal (Dick) School of Veterinary Studies, University of Edinburgh). OPA cases were obtained in conjunction with Dr. P. Scott (Capital Veterinary Services).

References

1. DiMasi JA, Hansen RW, Grabowski HG. The price of innovation: new estimates of drug development costs. J Health Econ. (2003) 22:151–85. doi: 10.1016/S0167-6296(02)00126-1

PubMed Abstract | CrossRef Full Text | Google Scholar

2. Kola I, Landis J. Can the pharmaceutical industry reduce attrition rates? Nat Rev Drug Discov. (2004) 3:711–6. doi: 10.1038/nrd1470

PubMed Abstract | CrossRef Full Text | Google Scholar

3. Daniel KD, Kim GY, Vassiliou CC, Galindo M, Guimaraes AR, Weissleder R, et al. Implantable diagnostic device for cancer monitoring. Biosens Bioelectr. (2009) 24:3252–7. doi: 10.1016/j.bios.2009.04.010

PubMed Abstract | CrossRef Full Text | Google Scholar

4. Masi BC, Tyler BM, Bow H, Wicks RT, Xue Y, Brem H, et al. Intracranial MEMS based temozolomide delivery in a 9L rat gliosarcoma model. Biomaterials. (2012) 33:5768–75. doi: 10.1016/j.biomaterials.2012.04.048

PubMed Abstract | CrossRef Full Text | Google Scholar

5. Gray ME, Meehan J, Blair EO, Ward C, Langdon SP, Morrison LR, et al. Biocompatibility of common implantable sensor materials in a tumor xenograft model. J Biomed Mater Res. (2018) 107:1620–33. doi: 10.1002/jbm.b.34254

PubMed Abstract | CrossRef Full Text | Google Scholar

6. Ferlay J, Soerjomataram I, Dikshit R, Eser S, Mathers C, Rebelo M, et al. Cancer incidence and mortality worldwide: sources, methods and major patterns in GLOBOCAN 2012. Int J Cancer. (2015) 136:359–86. doi: 10.1002/ijc.29210

PubMed Abstract | CrossRef Full Text | Google Scholar

7. Pozzi A. Mouse Models of Lung Cancer, Principles and Practice of Lung Cancer. 4th ed. Philadelphia, PA: Lippincott Williams and Wilkins (2010). p. 179–87.

Google Scholar

8. Lynch CJ. Studies on the relation between tumor susceptibility and heredity: III. Spontaneous tumors of the lung in mice. J Exp Med. (1926) 43:339–55. doi: 10.1084/jem.43.3.339

PubMed Abstract | CrossRef Full Text | Google Scholar

9. Szymanska H, Sitarz M, Krysiak E, Piskorowska J, Czarnomska A, Skurzak H, et al. Genetics of susceptibility to radiation-induced lymphomas, leukemias and lung tumors studied in recombinant congenic strains. Int J Cancer. (1999) 83:674–8. doi: 10.1002/(SICI)1097-0215(19991126)83:5<674::AID-IJC18>3.0.CO;2-M

PubMed Abstract | CrossRef Full Text | Google Scholar

10. Mase K, Iijima T, Nakamura N, Takeuchi T, Onizuka M, Mitsui T, et al. Intrabronchial orthotopic propagation of human lung adenocarcinoma—characterizations of tumorigenicity, invasion and metastasis. Lung Cancer. (2002) 36:271–6. doi: 10.1016/S0169-5002(02)00004-1

PubMed Abstract | CrossRef Full Text | Google Scholar

11. Kozaki KI, Miyaishi O, Tsukamoto T, Tatematsu Y, Hida T, Takahashi T, et al. Establishment and characterization of a human lung cancer cell line NCI-H460-LNM35 with consistent lymphogenous metastasis via both subcutaneous and orthotopic propagation. Cancer Res. (2000) 60:2535–40.

PubMed Abstract | Google Scholar

12. Kuo HT, Kubota T, Watanabe M, Furukawa T, Kase S, Tanino H, et al. Orthotopic reconstitution of human small-cell lung carcinoma after intravenous transplantation in SCID mice. Anticancer Res. (1992) 12:1407–10.

PubMed Abstract | Google Scholar

13. Paoloni MC, Khanna C Comparative oncology today The Veterinary clinics of North America. Small Anim Pract. (2007) 37:1023–31. doi: 10.1016/j.cvsm.2007.08.003

CrossRef Full Text | Google Scholar

14. Pang LY, Argyle DJ. Using naturally occurring tumours in dogs and cats to study telomerase and cancer stem cell biology, Biochim Biophys Acta (BBA). (2009) 1792:380–91. doi: 10.1016/j.bbadis.2009.02.010

PubMed Abstract | CrossRef Full Text | Google Scholar

15. DeMartini JC, York DF. Retrovirus-associated neoplasms of the respiratory system of sheep and goats: ovine pulmonary carcinoma and enzootic nasal tumor. Vet Clin. (1997) 13:55–70. doi: 10.1016/S0749-0720(15)30364-9

PubMed Abstract | CrossRef Full Text | Google Scholar

16. Palmarini M, Fan H, Sharp JM. Sheep pulmonary adenomatosis: a unique model of retrovirus associated lung cancer. Trends Microbiol. (1997) 5:478–83. doi: 10.1016/S0966-842X(97)01162-1

PubMed Abstract | CrossRef Full Text | Google Scholar

17. Griffiths DJ, Martineau HM, Cousens C. Pathology and pathogenesis of ovine pulmonary adenocarcinoma. J Comparat Pathol. (2010) 142:260–83. doi: 10.1016/j.jcpa.2009.12.013

PubMed Abstract | CrossRef Full Text | Google Scholar

18. Leroux C, Girard N, Cottin V, Greenland T, Mornex FJ, Archer F. Jaagsiekte Sheep Retrovirus (JSRV): from virus to lung cancer in sheep. Vet Res. (2007) 38:211–28. doi: 10.1051/vetres:2006060

PubMed Abstract | CrossRef Full Text | Google Scholar

19. Palmarini M, Fan H. Retrovirus-induced ovine pulmonary adenocarcinoma, an animal model for lung cancer. J Natl Cancer Inst. (2001) 93:1603–14. doi: 10.1093/jnci/93.21.1603

PubMed Abstract | CrossRef Full Text | Google Scholar

20. Marland RK, Blair EO, Flynn BW, González-Fernández E, Huang L, Kunkler IH, et al. Implantable Microsystems for Personalised Anticancer Therapy. In: CMOS Circuits for Biological Sensing and Processing, Cham: Springer International Publishing (2018). p. 259–86.

Google Scholar

21. Cousens C, Scott PR Assessment of transthoracic ultrasound diagnosis of ovine pulmonary adenocarcinoma in adult sheep Veterinary Record. (2015) 177:366–371. doi: 10.1136/vr.103298

CrossRef Full Text | Google Scholar

22. Scott PR, Dagleish MP, Cousens C. Development of superficial lung lesions monitored on farm by serial ultrasonographic examination in sheep with lesions confirmed as ovine pulmonary adenocarcinoma at necropsy. Irish Vet J. (2018) 71:23–9. doi: 10.1186/s13620-018-0134-0

PubMed Abstract | CrossRef Full Text | Google Scholar

23. Shrimpton PCJ, Jansen TM, Harrison JD. Updated estimates of typical effective doses for common CT examinations in the UK following the 2011 national review. Br J Radiol. (2016) 89:1–15. doi: 10.1259/bjr.20150346

PubMed Abstract | CrossRef Full Text | Google Scholar

24. Youssef G, Wallace WAH, Dagleish MP, Cousens C, Griffiths DJ. Ovine pulmonary adenocarcinoma: a large animal model for human lung cancer. Inst Lab Anim Res J. (2015) 56:99–115. doi: 10.1093/ilar/ilv014

PubMed Abstract | CrossRef Full Text | Google Scholar

25. Palmarini M, Sharp JM, Lee C, Fan H. In vitro infection of ovine cell lines by Jaagsiekte sheep retrovirus. J Virol. (1999) 73:10070–8.

PubMed Abstract | Google Scholar

26. Suau F, Cottin V, Archer F, Croze S, Chastang J, Cordier G, et al. Telomerase activation in a model of lung adenocarcinoma, Eur Resp J. (2006) 27:1175–82. doi: 10.1183/09031936.06.00125105

PubMed Abstract | CrossRef Full Text | Google Scholar

27. Archer F, Jacquier E, Lyon M, Chastang J, Cottin V, Mornex JF, et al. Alveolar type II cells isolated from pulmonary adenocarcinoma: a model for JSRV expression in vitro. Am J Resp Cell Molecul Biol. (2007) 36:534–40. doi: 10.1165/rcmb.2006-0285OC

PubMed Abstract | CrossRef Full Text | Google Scholar

28. Johnson C, Fan H. Three-dimensional culture of an ovine pulmonary adenocarcinoma-derived cell line results in re-expression of surfactant proteins and Jaagsiekte sheep retrovirus. Virology. (2011) 414:91–6. doi: 10.1016/j.virol.2011.03.018

PubMed Abstract | CrossRef Full Text | Google Scholar

29. Jassim F, Sharp J, Marinello P. Three-step procedure for isolation of epithelial cells from the lungs of sheep with jaagsiekte. Res Vet Sci. (1987) 43:407–9. doi: 10.1016/S0034-5288(18)30815-4

PubMed Abstract | CrossRef Full Text | Google Scholar

30. Martin WB, Scott FM, Sharp JM, Angus KW, Norval M. Experimental production of sheep pulmonary adenomatosis (Jaagsiekte). Nature. (1976) 264:183–7. doi: 10.1038/264183a0

PubMed Abstract | CrossRef Full Text | Google Scholar

31. Sharp J, Angus K, Gray E, Scott F. Rapid transmission of sheep pulmonary adenomatosis (jaagsiekte) in young lambs. Arch Virol. (1983) 78:89–95. doi: 10.1007/BF01310861

PubMed Abstract | CrossRef Full Text | Google Scholar

32. Murgia C, Caporale M, Ceesay O, Di Francesco G, Ferri N, Varasano V, et al. Lung adenocarcinoma originates from retrovirus infection of proliferating type 2 pneumocytes during pulmonary post-natal development or tissue repair. PLoS Pathog. (2011) 7:1–12. doi: 10.1371/journal.ppat.1002014

CrossRef Full Text | Google Scholar

33. Salvatori D, Gonzalez L, Dewar P, Cousens C, de las Heras M, Dalziel RG, et al. Successful induction of ovine pulmonary adenocarcinoma in lambs of different ages and detection of viraemia during the preclinical period. J General Virol. (2004) 85:3319–24. doi: 10.1099/vir.0.80333-0

PubMed Abstract | CrossRef Full Text | Google Scholar

34. Caporale M, Cousens C, Centorame P, Pinoni C, De las Heras M, Palmarini M. Expression of the jaagsiekte sheep retrovirus envelope glycoprotein is sufficient to induce lung tumors in sheep. J Virol. (2006) 80:8030–7. doi: 10.1128/JVI.00474-06

PubMed Abstract | CrossRef Full Text | Google Scholar

35. Linnerth-Petrik NM, Santry LA, Darrick LY, Wootton SK. Adeno-associated virus vector mediated expression of an oncogenic retroviral envelope protein induces lung adenocarcinomas in immunocompetent mice. PLoS ONE. (2012) 7:51400–15. doi: 10.1371/journal.pone.0051400

PubMed Abstract | CrossRef Full Text | Google Scholar

36. Vlachostergios PJ, Oikonomou KG, Gibilaro E, Apergis G. Elevated lactic acid is a negative prognostic factor in metastatic lung cancer. Cancer Biomark. (2015) 15:725–34. doi: 10.3233/CBM-150514

PubMed Abstract | CrossRef Full Text | Google Scholar

37. Wallace JM, Deutsch AL. Flexible fiberoptic bronchoscopy and percutaneous needle lung aspiration for evaluating the solitary pulmonary nodule. Chest. (1982) 81:665–71. doi: 10.1378/chest.81.6.665

PubMed Abstract | CrossRef Full Text | Google Scholar

38. Aristizabal JF, Young KR, Nath H. Can chest CT decrease the use of preoperative bronchoscopy in the evaluation of suspected bronchogenic carcinoma?, Chest. (1998) 113:1244–9. doi: 10.1378/chest.113.5.1244

PubMed Abstract | CrossRef Full Text | Google Scholar

39. Mazzone P, Jain P, Arroliga AC, Matthay RA. Bronchoscopy and needle biopsy techniques for diagnosis and staging of lung cancer. Clin Chest Med. (2002) 23:137–58. doi: 10.1016/S0272-5231(03)00065-0

PubMed Abstract | CrossRef Full Text | Google Scholar

40. Laurent F, Montaudon M, Latrabe V, Bégueret H. Percutaneous biopsy in lung cancer. Eur J Radiol. (2003) 45:60–8. doi: 10.1016/S0720-048X(02)00286-3

PubMed Abstract | CrossRef Full Text | Google Scholar

41. Schreiber G, McCrory DC. Performance characteristics of different modalities for diagnosis of suspected lung cancer: summary of published evidence. Chest. (2003) 123:115–28. doi: 10.1378/chest.123.1_suppl.115S

PubMed Abstract | CrossRef Full Text | Google Scholar

42. Gaeta M, Pandolfo I, Volta S, Russi EG, Bartiromo G, Girone G, et al. Bronchus sign on CT in peripheral carcinoma of the lung: value in predicting results of transbronchial biopsy. Am J Roentgenol. (1991) 157:1181–5. doi: 10.2214/ajr.157.6.1950861

PubMed Abstract | CrossRef Full Text | Google Scholar

43. Meeusen EN, Snibson KJ, Hirst SJ, Bischof RJ. Sheep as a model species for the study and treatment of human asthma and other respiratory diseases. Drug Discov Today. (2009) 6:101–6. doi: 10.1016/j.ddmod.2009.12.002

CrossRef Full Text | Google Scholar

44. House AJ, Thomson KR. Evaluation of a new transthoracic needle for biopsy of benign and malignant lung lesions. Am J Roentgenol. (1977) 129:215–20. doi: 10.2214/ajr.129.2.215

PubMed Abstract | CrossRef Full Text | Google Scholar

45. Klein JS, Zarka MA. Transthoracic needle biopsy. Radiol Clin North Am. (2000) 38:235–66. doi: 10.1016/S0033-8389(05)70161-5

PubMed Abstract | CrossRef Full Text | Google Scholar

46. W.-Liao Y, Chen ZM, Chang LY, Wu DH, Yu JC, Kuo HP, et al. US-guided transthoracic cutting biopsy for peripheral thoracic lesions less than 3 cm in diameter. Radiology. (2000) 217:685–91. doi: 10.1148/radiology.217.3.r00dc21685

CrossRef Full Text | Google Scholar

47. -Pan FJ, Yang PC, Chang DB, Lee CY, Kuo HS, Luh KT. Needle aspiration biopsy of malignant lung masses with necrotic centers: improved sensitivity with ultrasonic guidance. Chest. (1993) 103:1452–6. doi: 10.1378/chest.103.5.1452

PubMed Abstract | CrossRef Full Text | Google Scholar

48. Li H, Boiselle PM, Shepard JO, Trotman-Dickenson B, McLoud TC. Diagnostic accuracy and safety of CT-guided percutaneous needle aspiration biopsy of the lung: comparison of small and large pulmonary nodules. Am J Roentgenol. (1996) 167:105–9. doi: 10.2214/ajr.167.1.8659351

PubMed Abstract | CrossRef Full Text | Google Scholar

49. Connor S, Dyer J, Guest P. Image-guided automated needle biopsy of 106 thoracic lesions: a retrospective review of diagnostic accuracy and complication rates. Eur Radiol. (2000) 10:490–4. doi: 10.1007/s003300050082

PubMed Abstract | CrossRef Full Text | Google Scholar

50. Swischuk JL, Castaneda F, Patel JC, Li R, Fraser KW, Brady TM, et al. Percutaneous transthoracic needle biopsy of the lung: review of 612 lesions. J Vasc Int Radiol. (1998) 9:347–52. doi: 10.1016/S1051-0443(98)70279-9

PubMed Abstract | CrossRef Full Text | Google Scholar

51. Mueller PRE. vanSonnenberg, Interventional radiology in the chest and abdomen. N Engl J Med. (1990) 322:1364–74. doi: 10.1056/NEJM199005103221906

PubMed Abstract | CrossRef Full Text | Google Scholar

52. Daly B, Templeton PA. Real-time CT fluoroscopy: evolution of an interventional tool. Radiology. (1999) 211:309–15. doi: 10.1148/radiology.211.2.r99ma51309

PubMed Abstract | CrossRef Full Text | Google Scholar

53. Cox JE, Chiles C, McManus CM, Aquino SL, Choplin RH. Transthoracic needle aspiration biopsy: variables that affect risk of pneumothorax. Radiology. (1999) 212:165–8. doi: 10.1148/radiology.212.1.r99jl33165

PubMed Abstract | CrossRef Full Text | Google Scholar

54. Fish GD, Stanley JH, Miller KS, Schabel SI, Sutherland SE. Postbiopsy pneumothorax: estimating the risk by chest radiography and pulmonary function tests. Am J Roentgenol. (1988) 150:71–4. doi: 10.2214/ajr.150.1.71

PubMed Abstract | CrossRef Full Text | Google Scholar

55. Haramati LB, Austin J. Complications after CT-guided needle biopsy through aerated versus nonaerated lung. Radiology. (1991) 181:778. doi: 10.1148/radiology.181.3.1947096

PubMed Abstract | CrossRef Full Text | Google Scholar

56. Lim CS, Tan LE, Wang JY, Lee CH, Chang HC, Lan CC, et al. Risk factors of pneumothorax after CT-guided coaxial cutting needle lung biopsy through aerated versus nonaerated lung. J Vascul Int Radiol. (2014) 25:1209–17. doi: 10.1016/j.jvir.2014.03.031

PubMed Abstract | CrossRef Full Text | Google Scholar

57. Saji H, Nakamura H, Tsuchida T, Tsuboi M, Kawate N, Konaka C, et al. The incidence and the risk of pneumothorax and chest tube placement after percutaneous CT-guided lung biopsy: the angle of the needle trajectory is a novel predictor: the angle of the needle trajectory is a novel predictor. Chest. (2002) 121:1521–6. doi: 10.1378/chest.121.5.1521

PubMed Abstract | CrossRef Full Text | Google Scholar

58. Moore EH, Shepard JA, McLoud TC, Templeton PA, Kosiuk JP. Positional precautions in needle aspiration lung biopsy. Radiology. (1990) 175:733–5. doi: 10.1148/radiology.175.3.2343123

PubMed Abstract | CrossRef Full Text | Google Scholar

59. Ko JP, Shepard JAO, Drucker EA, Aquino SL, Sharma A, Sabloff B, et al. Factors influencing pneumothorax rate at lung biopsy: are dwell time and angle of pleural puncture contributing factors? Radiology. (2001) 218:491–6. doi: 10.1148/radiology.218.2.r01fe33491

PubMed Abstract | CrossRef Full Text | Google Scholar

60. Covey AM, Gandhi R, Brody LA, Getrajdman G, Thaler HT, Brown KT. Factors associated with pneumothorax and pneumothorax requiring treatment after percutaneous lung biopsy in 443 consecutive patients. J Vasc Int Radiol. (2004) 15:479–83. doi: 10.1097/01.RVI.0000124951.24134.50

PubMed Abstract | CrossRef Full Text | Google Scholar

61. Kazerooni EA, Lim FT, Mikhail A, Martinez FJ. Risk of pneumothorax in CT-guided transthoracic needle aspiration biopsy of the lung. Radiology. (1996) 198:371–5. doi: 10.1148/radiology.198.2.8596834

PubMed Abstract | CrossRef Full Text | Google Scholar

62. Shrimpton PC, Jessen KA, Geleijns J, Panzer WG. Tosi reference doses in computed tomography. Radiation Protec Dosimet. (1998) 80:55–9. doi: 10.1093/oxfordjournals.rpd.a032542

CrossRef Full Text | Google Scholar

63. Yang K, Ganguli S, DeLorenzo MC, Zheng H, Li X, Liu B. Procedure-specific CT dose and utilization factors for CT-guided interventional procedures. Radiology. (2018) 289:150–7. doi: 10.1148/radiol.2018172945

PubMed Abstract | CrossRef Full Text | Google Scholar

64. Tomiyama N, Yasuhara Y, Nakajima Y, Adachi S, Arai Y, Kusumoto M, et al. CT-guided needle biopsy of lung lesions: a survey of severe complication based on 9783 biopsies in Japan. Eur J Radiol. (2006) 59:60–4. doi: 10.1016/j.ejrad.2006.02.001

PubMed Abstract | CrossRef Full Text | Google Scholar

65. Klein JS, Salomon G, Stewart EA. Transthoracic needle biopsy with a coaxially placed 20-gauge automated cutting needle: results in 122 patients. Radiology. (1996) 198:715–20. doi: 10.1148/radiology.198.3.8628859

PubMed Abstract | CrossRef Full Text | Google Scholar

66. Ng YL, Patsios D, Roberts H, Walsham A, Paul NS, Chung T, et al. CT-guided percutaneous fine-needle aspiration biopsy of pulmonary nodules measuring 10 mm or less. Clin Radiol. (2008) 63:272–7. doi: 10.1016/j.crad.2007.09.003

CrossRef Full Text | Google Scholar

67. Yeow KM, See LC, Lui KW, Lin MC, Tsao TCY, Ng KF, et al. Risk factors for pneumothorax and bleeding after CT-guided percutaneous coaxial cutting needle biopsy of lung lesions. J Vascul Intervent Radiol. (2001) 12:1305–12. doi: 10.1016/S1051-0443(07)61556-5

PubMed Abstract | CrossRef Full Text | Google Scholar

68. Khan MF, Straub R, Moghaddam SR, Maataoui A, Gurung J, Wagner TO, et al. Variables affecting the risk of pneumothorax and intrapulmonal hemorrhage in CT-guided transthoracic biopsy. Eur Radiol. (2008) 18:1356–63. doi: 10.1007/s00330-008-0893-1

PubMed Abstract | CrossRef Full Text | Google Scholar

69. Heyer CM, Reichelt S, Peters SA, Walther JW, Muller KM, Nicolas V. Computed tomography-navigated transthoracic core biopsy of pulmonary lesions: which factors affect diagnostic yield and complication rates? Academ Radiol. (2008) 15:1017–26. doi: 10.1016/j.acra.2008.02.018

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: human lung cancer, ovine pulmonary adenocarcinoma, novel translational lung cancer model, pre-clinical research, computed tomography-guided sensor implantation

Citation: Gray ME, Sullivan P, Marland JRK, Greenhalgh SN, Meehan J, Gregson R, Clutton RE, Cousens C, Griffiths DJ, Murray A and Argyle D (2019) A Novel Translational Ovine Pulmonary Adenocarcinoma Model for Human Lung Cancer. Front. Oncol. 9:534. doi: 10.3389/fonc.2019.00534

Received: 05 April 2019; Accepted: 03 June 2019;
Published: 19 June 2019.

Edited by:

Kyle Schachtschneider, University of Illinois at Chicago, United States

Reviewed by:

Ramon A. Juste, Servicio Regional de Investigación y Desarrollo Agroalimentario (SERIDA), Spain
Hung Fan, University of California, Irvine, United States

Copyright © 2019 Gray, Sullivan, Marland, Greenhalgh, Meehan, Gregson, Clutton, Cousens, Griffiths, Murray and Argyle. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Mark E. Gray, s9900757@sms.ed.ac.uk