microRNA: diagnostic perspective
- Division of Pathology, Department of Clinical and Molecular Medicine, Faculty of Medicine and Psychology, Ospedale Santo Andrea, Sapienza University of Rome, Rome, Italy
Biomarkers are biological measures of a biological state. An ideal marker should be safe and easy to measure, cost efficient, modifiable with treatment, and consistent across gender and ethnic groups. To date, none of the available biomarkers satisfy all of these criteria. In addition, the major limitations of these markers are low specificity, sensitivity, and false positive results. Recently identified, microRNAs (miRNAs) are endogenous, evolutionarily conserved small non-coding RNA (about 22–25 nt long), also known as micro-coordinators of gene expression, which have been shown to be an effective tools to study the biology of diseases and to have great potential as novel diagnostic and prognostic biomarkers with high specificity and sensitivity. In fact, it has been demonstrated that miRNAs play a pivotal role in the regulation of a wide range of developmental and physiological processes and their deficiencies have been related to a number of disease. In addition, miRNAs are stable and can be easily isolated and measured from tissues and body fluids. In this review, we provide a perspective on emerging concepts and potential usefulness of miRNAs as diagnostic markers, emphasizing the involvement of specific miRNAs in particular tumor types, subtypes, cardiovascular diseases, diabetes, infectious diseases, and forensic test.
The ideal biomarker should be non-invasive, specific, cost efficient, quantifiable, robust, translatable, predictive, and sensitive. Physicians, Scientists, and epidemiologists use biomarkers for monitoring, screening, diagnostics, and prognostics of various diseases (1). It is established that disease-related biomarkers including proteins (antigens, enzymes), lipid, and electrolyte components, could be segregated from cells or tissues with current disease and exist in the blood (2). Current available serum/plasma biomarkers are mostly based on proteins. The major limitations of these markers are low specificity, sensitivity, and false positive results. One example among many is given by the serum prostate-specific antigen (PSA), which has been used for screening men with an existing diagnosis of prostate cancer (PCa) and is used as a marker for identifying recurring disease subsequent to treatment. However, PSA-based screening is also associated with over diagnosis and overtreatment. The fact that PSA is synthesized by all prostate epithelial cells, whether normal, hyperplastic, or cancerous, weakens the specificity of PSA as a cancer biomarker. Elevated serum PSA levels may reflect the presence of cancer or may be caused by benign prostatic hyperplasia (BPH), infection, and chronic inflammation (3).
microRNAs (miRNAs) are endogenous, evolutionarily conserved, naturally abundant, relatively stable, small (about 22 nt long) non-coding RNA molecules that function as post-transcriptional gene regulation in most biological and pathological process (4, 5).
It has been estimated that over 30% of protein-coding genes are regulated by miRNAs either by complementary binding of target mRNA or binding to imperfect complementary sites in the 3′ untranslated regions (3′UTR), leading to control of expression of these genes at the level of translation (4, 6, 7). It has been also calculated that above 45,000 miRNAs target sites are present in the human 3′UTR and above 60% of human protein-coding genes are probably regulated by multiple miRNAs (8). miRNAs are transcribed in the nucleus as a long, capped, poly-adenylated precursor called primary miRNA (pri-miRNA) by a RNA polymerase II or III (9, 10). This pri-miRNA is processed by the ribonuclease (RNase) III called Drosha or the double-stranded DNA-binding Protein called DGCR8/Pasha (11) producing a precursor miRNA (pre-miRNA). The nuclear export receptor exportin 5/Ran GTP actively transports pre-miRNAs to the cytoplasm (12, 13). Then, Pre-miRNAs are processed by the RNase III endonuclease Dicer along with the trans-activation-responsive RNA-binding protein (TRBP) and produced a small double-stranded RNA structure (22 nt). This duplex miRNA is unwound into mature single-stranded form and integrate into the RNA-induced silencing complex (RISC), which escorts the complex into the complementary 3′UTR of the target mRNA.
In 2008, circulating miRNAs were identified in blood plasma, platelets, leukocytes, and erythrocytes. Even in the adverse conditions (high or low PH, boiling, freeze–thaw cycle, and long-term storage at room temperature), plasma miRNAs were found to be stable (14, 15). Recently, several studies suggested that plasma miRNAs may be packaged into the exosomes, microvesicles, and apoptotic bodies or associated with the RNA-binding proteins (Arogonaute2) or lipoprotein complex (HDL) to protect their degradation from RNase. Circulating miRNA may mediate distant cell–cell communication, probably to regulate gene expression (16, 17).
Most interestingly, circulating miRNAs have many necessary features of ideal biomarkers. Stable miRNAs have been found in various biological fluids, such as plasma, serum, saliva, milk, cerebrospinal fluids, and markedly expression motifs of serum miRNAs, are firmly linked to various diseases including cancer. The quantity of miRNAs can be easily estimated by various methods, such as Microarray, Hybridization, Deep-sequencing, qRT-PCR, and microbeads analysis.
microRNAs have been demonstrated to play a major role in a wide range of developmental processes including metabolism, apoptosis, cell proliferation, stem cell division, muscle differentiation, and brain morphogenesis (18–20). Since this pivotal role in the regulation of these processes related to development and other physiological functions, miRNAs deficiencies have been linked to a number of diseases ranging from cancer to autoimmune disease.
The aim of this review is to emphasize the great potential of circulating miRNAs as very specific and sensitive biomarkers for diagnosis of tumor and other diseases.
miRNAs in Diagnosis of Cancer
During the present time, circulating miRNAs are going to the new era of cancer diagnosis and prognosis. Anomalous levels of extracellular miRNAs have been assessed in several cancers, such as hematological and solid neoplasms (summarized in Table 1).
In 2008, Lawrie et al. showed that levels of serum miRNA-21were associated with diagnosis and prognosis in diffuse large B-cell lymphoma (DLBCL) patients (21). More recently, Chen et al. confirmed these results in the sera of Chinese DLBCL patients compared to healthy controls (47). Acute myeloid leukemia (AML) is another type of common hematological cancer in adults. Fayyad-Kazan et al. showed that the expression of two important plasma miRNAs (miR-150 andmiR-342) was up-regulated compared to healthy controls, suggesting that these two miRNAs could be novel, potential, and specific biomarkers for early diagnosis of AML (22). Besides DLBCL and AML, extracellular miRNAs have been also reported in chronic lymphocytic leukemia (CLL). A recent study demonstrated that circulating miR-195, miR-29a, and miR-222 levels are the better indicators to separate B-cell CLL patients from healthy controls (48). In addition, high level of plasma miR-155 seems to be an early detector of the disease (23).
The most common type of lung cancer, non-small cell lung cancer (NSCLC), can be diagnosed in various stages using cell-free non-invasive miRNAs.
Recently, two validated serum miRNAs (miR-25 and miR-223) have been reported to be involved in the tumorigenic process and significantly increased in NSCLC patients, suggesting their potential use in early diagnosis of this lethal neoplasm (15).
Different studies focused on the identification of plasma and serum miRNAs signatures, which could exploit as early stage diagnostic markers for NSCLC. For example, serum-based two miRNAs panel (miR-1254, miR-574-5p) is significantly increased in early stage NSCLC (24), and a plasma based three miRNAs panel (miR-155, miR-197, miR-182) is notably increased in stage-I NSCLC (25). A plasma based four miRNAs panel (miR-21, miR-126, miR-210, miR-182) is differentially expressed in stage-I NSCLC; and furthermore, this panel can be used for differentiate lung adenocarcinoma from squamous cell cancer (49). Lastly, a serum-based 10 miRNAs panel (miR-20a, miR-24, miR-25, miR-145, miR-152, miR-199a-5p, miR-211, miR-222, miR-223, miR-320) is significantly and differentially expressed in early NSCLC patients (50).
Cancer of the PCa is now recognized as one of the most important medical problems facing the male population. Historically, serum PSA has been used for screening men with an existing diagnosis of PCa and has been regarded as an ideal marker for identifying recurring disease subsequent to treatment (51). However, PSA-based screening is associated with over diagnosis and overtreatment (52).
Although Mitchell et al. first reported that serum miR-141 is very sensitive biomarkers to detect PCa, different and contradictory results were obtained by Mahn and co-authors (14, 53). Other studies showed that extracellular miR-375 and miR-141 were most optimistic markers in the diagnosis of this neoplasm (26). Urine, another important source of circulating miRNA, has been widely exploited for the diagnosis of urological cancer. Bryant et al. showed that miRs 107 and 574-3p were significantly higher in the urine of PCa patients compared to healthy groups, and would perform even better than PCA3 normalized to PSA in identifying the presence of PCa (27). Other recent studies reported that urine miR-205 and miR-214 were significantly down-regulated in PCa patients with 80% specificity and 89% sensitivity (28).
Pancreatic cancer is the fourth most common cause of cancer death in the Western world. The prognosis is poor, with 1- and 5-year survival rates of only 20 and 6%. Early diagnosis of pancreatic cancer is difficult, and no biomarkers in blood can identify patients with pancreatic cancer at an early stage. In a recent and promising study, Schultz and colleagues identified two diagnostic panels based on miRNA expression in whole blood with the potential to distinguish patients with pancreatic cancer from healthy controls (29).
Hepatocellular carcinoma (HCC), a form of primary liver cancer, tends to develop in a setting of chronic infection with HBV or HCV viruses, genetic defects, liver injury, or alcohol misuses. Several studies have tried to use extracellular miRNAs for distinguish HCC from other liver disease. Qu et al. reported that serum miR-16 and miR-199a are significant and specifically decreased in HCC compared to chronic liver disease patients. In addition they demonstrated that combining miR-16 with AFP and Lens culinaris agglutinin-reactive AFP (AFP-L3) tumor markers could increase sensitivity and specificityin the diagnosisofHCC (30). MiR-15b, miR-130b, and miR-16 are potential, specific diagnostic markers in discriminate between HCC and HBV hepatitis patients, and for early detection of liver cancer as compared to others serum cancer biomarkers such as AFP, des-γ-carboxyprothrombin (DCP), and AFP-L3 (31, 32).
Recently, Abdalla et al. showed that in urine sample, the levels of three miRNAs (miR-625, miR-618, miR-532) are high and levels of two miRNAs (miR-650, miR-516-5p) are very low as compared to the HCC (HCV positive) group and the control groups (33).
Colorectal cancer (CRC) is the third most commonly diagnosed cancer and the third cardinal cause of cancer death in the world. Early diagnosis may risk-free of CRC and can easier target therapy. In several ongoing studies, miRNAs showed to be promising sensitive and specific early detecting molecular biomarkers. Up to date, plasma levels of miR-29a and miR-92 are significantly increased whereas levels of miR-601 and miR-760 are significantly decreased in the early stage of CRC as compared to healthy individuals (34, 35). Recently, Wang et al. reported that inCRC, four cell-free miRNAs (miR-31, miR-181b, miR-92, miR-203) are down-regulated and two miRNAs (miR-21, let-7g) are up-regulated, being more sensitive and specific in the identification of CRC than any single protein biomarker like CEA or CA19-9 (36). Moreover, has been reported that a combination of seven exosomal miRNAs (let-7a, miR-23a, miR-21, miR-150, miR-223, and miR-1229) might be used for early detection of CRC, being significantly increased as compared to healthy groups. In addition, high levels of serum miR-200c in CRC patients have been reported to have a powerful interrelationship with lymph node metastasis (37).
Gastric cancer (GC) is another leading cause of cancer death in the world. For GC diagnosis, fewer numbers of sensitive and specific markers are available. Several studies showed that many extracellular miRNAs are promising and sensitive specific biomarker for early diagnosis of GC (54). More recently, Tsujiura et al. reported that plasma levelsof miR-18a are significantly increased in GC patients (38). In addition, a five miRNAs panel (miR-16, miR-25, miR-92a, miR-451, and miR-486-5p) was identified in plasma as a potential biomarker for early diagnosis of GC (55). Moreover, another study showed that the plasma miR-122 was down-regulated and plasma miR-192 was up-regulated in GC patients and might be used for the early diagnosis of distant metastasis (39).
Briefly, circulating miRNAs have been proven to be useful diagnostic/prognostic markers in other tumors. A two miRNAs signature (high levels of miR-205 and low levels of miR-let-7f) in the plasma of epithelial ovarian cancer (EOC) patients could be able to identify with high specificity and sensitivity EOC patients eventually stage-I disease (40), improving their chances of therapeutic intervention.
Many individual circulating miRNA showed significant association with early cancer diagnosis’s, such as miR-21 levels, that increase in esophageal cancer patients and interestingly together with ROS analysis could be diagnostic for biliary tract cancer (BTC), miR-210 levels are increased in conventional renal cell carcinoma (cRCC) patients, miR-218 levels are significantly reduced in advance stage cervical cancer, cervical adenocarcinoma, and lymphatic metastasis (41–43, 56, 57). In addition, a three miRNAs panel (let-7f, miR-151-5p and miR-222) are significantly up-regulated in sera of papillary thyroid cancer (PTC) patients (44). Moreover, a seven miRNAs panel (miR-15b*, miR-23a, miR-133a, miR-150*, miR-197, miR-497, and miR-548b-5p) is notably reduced in astrocytomas patients, with high sensitivity (88.00%) and specificity (97%) (45).
Furthermore, saliva two miRNAs (miR-125a, miR-200a) were found in reduced in oral squamous cell carcinoma patients. In addition, two validated urine miRNAs (miR-125b and mir-126) are indicated as, highly sensitive (80%), specific (100%), and non-invasive biomarker for bladder cancer diagnosis and prognosis (46).
miRNA Signatures Can Differentiate between Tumor Subtype
Formalin-fixed paraffin-embedded (FFPE) tissues are a very valuable source for biomarker discovery and validation. Quantity, quality, and the integrity of mRNA into FFPE tissues are not optimal due degradation or cross-linking with proteins and various chemical (58, 59). miRNAs are small size and potentially more stable to degradation than mRNAs during the formalin fixing procedures. Recently, many studies supported and proved that miRNAs are minimally affected by FFPE and, for example, can be simply detected by qRT-PCR in archived liver and CRC specimens up to 30 and 10 years, respectively (60–62).
Identification of tumor subtype is instrumental for patient treatment and therefore survival and the peculiar patterns of miRNAs expression in the individual type of tumor can boost this classification (Table 2).
Breast cancer is a highly heterogeneous disease with different molecular alteration, which result in its classification into five intrinsic subtypes (luminal A and B, HER2-enriched, basal-like and normal-like) (75, 76). The original molecular classification is based on investigations on frozen tissue, and it is not applicable to FFPE material, jeopardizing the wide application in the clinical practice. Recently, several studies reported that deregulation of miRNAs expression was strongly associated to molecular breast cancer subtype. In fact, in plasma, the combination of our (miR-29a, miR-181a, miR-223, miR-652) down-regulated and three (miR-29a, miR-181a, miR-652) up-regulated miRNAs was significantly and reliably associated with luminal A tumor (63). Tissue miRNA-342 was highly expressed in luminal B tumor and regarded as a very sensitive and specific biomarker this type of breast cancer (64). Moreover, other miRNAs have been identify to distinguish the remaining subtypes, such as basal-like (miR-18a, miR-135b, miR-93, and miR-155), HER2 type (miR-142-3p, and miR-150), and normal-like (miR-145, miR-99a, miR-100, miR-130) (63–66, 75, 76).
Renal tumors have different genetic backgrounds, prognoses, and responses to surgical and medical treatment, and their differential diagnosis is a frequent challenge for pathologists. Recently, Youssef et al. developed a classification system that can identify the different renal cell carcinoma (RCC) among four subtypes [RCC clear cell RCC (ccRCC), papillary RCC (pRCC), oncocytoma and chromophobe RCC (cRCC)] using a tissue-specific miRNAs signature analysis. This method showed a sensitivity of 97% in discriminating normal from RCC patients, 97% for pRCC from chRCC and oncocytoma, 100% for the ccRCC subtype vs. others subtype and chRCC vs. oncocytoma (67).
The remarkably heterogeneous nature of lung cancer has become more apparent over the last decade. In general, advanced lung cancer is an aggressive malignancy with a poor prognosis. Each subtype is associated with molecular tests that define the subtype and drugs that may potentially treat it.
Gilad et al. proved that eight miRNAs have high accuracy (overall 94%), and high sensitivity (overall 96%) to distinguish among the four subtypes of lung cancer [small cell lung cancer (SCLC), NSCLC, squamous cell carcinoma and carcinoid] (77). Hsa-miR-21 and miR-29b are expressed at higher levels in NSCLC versus SCLC and miR-129-3p, miR-205 can be utilized to differentiate squamous from non-squamous NSCLC (68, 69).
Diffuse large B-cell lymphoma is a common form of high-grade non-Hodgkin lymphoma (NHL) that account for 30–40% of all lymphoid malignancies. DLBCL includes a biologically and clinically diverse set of diseases, many of which cannot be separated from one another by well-defined criteria.
Many studies now suggest that DLBCL can be separated into two groups on the basis of their gene expression profiles: activated B cell-like (ABC) and germinal center B cell like (GCB). Recently, miRNAs have been used for characterization of DLBCL subtypes. Lawrie et al. reported that three miRNAs (miR-21, miR-155, and miR-221) are significantly expressed in DLBCL cases of ABC subtype as compared with GCB (70). Lim et al. demonstrated that miR-10393-3p is significantly over-expressed in DLBCL patients (71). Moreover, two miRNAs (miR-10397-5p, NOVELMOO288M) can distinguish ABC-DLBCL patients from other DLBCL patients (71). Furthermore, miR-5586-5p can be used for distinguish GCB-DLBCL from ABC-DLBCL, and miR-30b can also be used to discriminate GCB-DLBCL from other DLBCL disease group (71).
Peripheral T-cell lymphoma (PTCL) is a NHL, which refers to a diverse group of uncommon and aggressive nodal, extra nodal, and leukemic tumors that represent about 10–15% of all lymphoid neoplasm. The most common subtypes of PTCL are PTCL not otherwise specified (PTCL-NOS), angioimmunoblastic T-cell lymphoma (AITL), anaplastic large-cell lymphoma (ALCL) anaplastic lymphoma kinase present (ALK+), and ALCL/ALK− (72, 78). Specifically, PTCL-NOS is a rare and life-threatening disease whose differential diagnosis from AITL and ALCLs are still challenging. Most recently, Laginestra et al. validated a five miRNAs set (miR-515-3p, miR-155, miR-598, miR-625, miR-199a-5p) that can differentiate PTCL-NOS from ALCL/ALK−, a eight miRNAs panel (miR-652, miR-627, miR-519e, miR-487b, miR-324-5p, miR-449a, miR-381, miR-574-3p) that can be used to distinguish PTCL-NOS from AITL, and also a four miRNAs signature (miR-124, miR-325, miR-181a, miR-618) that can be used to identify ALCL/ALK− from ALCL/ALK+ disease group (72). Liu et al. confirmed two miRNA signatures that can be used as a diagnostic tool for biological difference of PTCLs sub-typing, and can play a crucial role in pathogenesis. In the first miRNA signature, the levels of five miRNAs (miR-512-3p, miR-886-5p, miR-886-3p, miR-708, miR-135b) are up-regulated, and levels of two miRNAs (miR-146a, miR-155) are down-regulated as compared to ALCL/ALK+ disease group from ALCL/ALK−, and other PTCLs disease group (73). Moreover, the second miRNA signature is used to differentiate ALCL/ALK− from ALCL/ALK+, and other PTCLs disease group (Table 2) (73).
miRNAs in Diagnosis in Other Diseases
Cardiovascular diseases (CVD) still represent the primary cause of morbidity and mortality worldwide. The understanding and the identification of CVD molecular factors that may significantly reduce the patient death rates still remain a challenge (74). Protein biomarkers, such as cardiac troponin (cTn), CK-MB, brain natriuretic peptide (BNP), and N-terminal prohormone (NT-proBNP), have been used to identify and monitor myocardial damage. Unfortunately, these biomarkers provided false positive results and are also time-dependent (79, 80). Therefore, for early diagnosis of cardiac damage other types of biomarker are the need of the hour. miRNAs have been proven to have an important role in CVD, including acute myocardial infarction (AMI), hypertrophy, heart failure, arrhythmias, and atherosclerosis (81). Tijsen et al. demonstrated that blood miR-423-5p was highly expressed in heart failure patients (independent of age and gender) and might represent a significant and sensitive biomarker for heart disease (82). Recently, it has been reported that elevated plasma levels of this miR are positively linked with NT-proBNP levels in dilated cardiomyopathy heart failure patients (83).
D’Alessandra et al. reported that plasma levels of miR-1, miR-133a/b were elevated 156 ± 72 min after the onset AMI symptoms; whereas plasma levels of miR-122 and miR-375 were lower only ST-segment elevation myocardial infarction (STEMI) patients than in healthy controls (84). Other studies showed that plasma levels of miR-21, miR-1, miR-26, miR-133, miR-30, miR-328, and miR-499 were significantly expressed in atrial fibrillation (85).
Takotsubo cardiomyopathy (TTC), a type of non-ischemiccardio myopathy unrelated to AMI, is a major life-threatening condition. To date, there are not early biomarker for its diagnosis and its distinction from AMI. Jaguszewski et al. reported that a unique signature comprising miR-1, miR-16, miR-26a, and miR-133a is capable of distinguish TTC from healthy individuals (sensitivity 74.19%, specificity78.57%) and from AMI patients (sensitivity 96%, specificity70.37%) (86).
Diabetes mellitus (DM) is a metabolic shuffle identified by hyperglycemia-mediated life-threatening complications. Many studies showed that circulating miRNAs are linked with type 1, 2, and gestational DM and its complications. Levels of circulating miR-21 and miR-210 were significantly high in the plasma and urine of the type 1 diabetic patients, while in urine miR-126 was notably lower in type-1 diabetic patients compare to controls (87). Peng et al. showed that the levels of urinary miR-29a were significantly high in albuminuria with type 2 DM than in healthy controls and urinary miR-29b was correlated with carotid intima-media thickness (cIMT) in patients with type 2 diabetes (88). In addition, the levels of platelet and plasma miR-223 and miR-146a were significantly reduced in patients with ischemic stroke and DM or only DM (89). Recently, Luo et al. demonstrated that platelet-derived miR-103b was specifically, down-regulated in early type 2 DM (90).
HIV/AIDS is a spectrum of conditions caused by infection with the human immunodeficiency virus type 1 and 2. For diagnosis of HIV/AIDS, several types of tests can help the physician to determine the patients HIV infection status, to calculate the evolution of the disease, and to monitor the efficacy of anti-retroviral therapy. Several studies demonstrated that host–virus interactions (including HIV) are controlled, at least in part, by miRNAs and these might lead to new diagnostic and attractive therapeutic strategies. Recently, Monteleone et al. proved that plasma miR-29b was highly expressed in HIV-1 patients, while lower levels of plasma miR-29cindicated high viremia, low CD4+ T cell count and high levels of integrated HIV-1 DNA, suggesting that the miR-29 family could be implicated in the natural history of HIV-1 infection (91). Another group reported that plasma levels of two miRNAs (miR-150 and miR-146b-5p) also varied between different groups ofHIV patients and between patients and healthy individuals (92). Moreover, expression levels of miR-150 in peripheral blood mononuclear cells (PBMCs) and plasma might be a better and specific biomarker for diagnosis of the different status of HIV/AIDS disease. MiR-150 levels were decreased in PBMCs but increased in plasma of HIV patients and drug-resistant HIV patients. On the other hand, miR-150 levels were increased in PBMCs and decreased in plasma of anti-retroviral therapy patients (92). In addition, Sekar et al. reported that miR-21 over-expression is considerably associated with the onset of HIV-related lymphomas (93). Furthermore, the levels of extracellular miR-122 were highly expressed in HIV/HCV co-infected patients (94).
Use of miRNAsin Forensic Diagnostic
Isolating the origin of body fluids in a crime scene would be instrumental for its reconstruction; however, conventional protein based methods for body fluid identification are prone to various limitations, such as sample consumption, varying degrees of sensitivity and specificity, and for mRNA based markers, stability.
The shorter lengths of miRNAs make them less susceptible to degradation caused by chemical and/or physical environmental factors, thus rendering them useful biomarkers for body fluid identification.
Hanson et al. showed the expression of miRNAs in dried forensically relevant biological fluids: blood, saliva, menstrual blood, and vaginal secretion. They distinguished nine panels of miRNAs that are differentially expressed and can be used as sensitive biomarkers to identify the origin of body fluid of forensic biological stains (95) (Table 3).
Experimental Techniques and Normalization of Circulating microRNAs
Accurate measurement of tissue and body fluid miRNAs has clinical importance for diagnosis and prognosis of several types of disease. miRNAs detection is a very challenging task for their native properties, e.g., small size, scarce concentration, high risk of cross-hybridization, and tissue/stage-specific expression. Therefore, quantification of cell-free miRNAs needs powerful tools. The rapid improvement of diagnostic device platforms is one of the leading experimental goals in the world of life science research and medical diagnostics. The explosion of high interest in miRNAs, over the recent years, brought to the development of many platforms. High-throughput miRNA profiling techniques including qRT-PCR, microarray, deep sequencing or next generation sequencing (NGS), and nanopores are effective tools for obtaining expression profiles of extracellular miRNAs. These techniques highly smoothen the process of free cell miRNA expression profiling. In this view, high-throughput techniques are better to the existing low-throughput techniques such as northern bolting and in situ hybridization (ISH) (96). Currently, qRT-PCR is the most common, reliable and available, inexpensive method used for quantifying the small amount of miRNAs with the high sensitivity and specificity and the subsequent validation of clinical samples (96, 97). However, some limitations of qRT-PCR, such as normalization of data and primer design, can highly influence the results. The lack of standardized housekeeping RNA for normalization, especially in body fluid, is a critical issue (97). Many miRNAs can be used as control reference such as miR-16, miR-142-3p, miR-30b, miR-145, miR-93, U6, U6B, SNORD68, RNU48, RNU43, RNU62, and 5sRNA. Kirschner et al. reported that miR-16 is highly expressed in red blood cells and that its levels in the extracellular content of blood fluids can differ significantly due to hemolysis (98). Moreover, many studies suggested that several endogenous genes might be diseases specific. Therefore, some miRNAs, such as miR-16 and miR-93 and SNORD68, might be considered satisfactory reference gene for miRNAs serum analysis of gastric and urologic cancers, respectively (99, 100). At present, there is no unique housekeeping RNA that can be used as the standard endogenous reference gene in normalizing circulating miRNAs. Currently, many studies suggest the use of more than one reference genes or better a combination for normalizing circulating miRNA concentrations.
An optimal biomarker should be sensitive, specific, non-invasive, and comparable to the disease conditions. In the new decade, many studies clearly proved that cell-free, miRNAs, and tissue miRNAs fulfill these expectations.
Despite the encouraging progress in the practical areas, several major theoretical and technical difficulties remain to be addressed. First, more basic investigations will be required to further examine the functional role of miRNAs in cancer, cardiovascular, and other disease. Although, miRNAs can inhibit mRNAs by translational repression or cleavage, others possible unknown mechanism could lead to translational or post-translation repression. Second, the biological functions and packaging of extracellular miRNAs needs to be better elucidated. A limited number of studies proposed that microvesicles containing miRNAs might be involved in the tumor microenvironment. Finally before translation into clinical practice, all circulating miRNA findings require further steps of validation and an accurate standardization of all preanalytical and analytical procedures, in order to control for all potential technical biases.
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
This work was supported by grants from PRIN (2010w4J4RM_004) and from grant RF-2010-2309704.
2. Dbouk HA, Tawil A, Nasr F, Kandakarjian L, Abou-Merhi R. Significance of CEA and VEGF as diagnostic markers of colorectal cancer in Lebanese patients. Open Clin Cancer J (2007) 1:1. doi:10.2174/1874189400701010001
11. Ambros V, Lee RC. Identification of microRNAs and other tiny noncoding RNAs by cDNA cloning. In: Gott JM, Clifton NJ, editors. RNA Interference, Editing, and Modification. Springer (2004). p. 131–58.
14. Mitchell PS, Parkin RK, Kroh EM, Fritz BR, Wyman SK, Pogosova-Agadjanyan EL, et al. Circulating microRNAs as stable blood-based markers for cancer detection. Proc Natl Acad Sci U S A (2008) 105(30):10513–8. doi:10.1073/pnas.0804549105
15. Chen X, Ba Y, Ma L, Cai X, Yin Y, Wang K, et al. Characterization of microRNAs in serum: a novel class of biomarkers for diagnosis of cancer and other diseases. Cell Res (2008) 18(10):997–1006. doi:10.1038/cr.2008.282
16. Arroyo JD, Chevillet JR, Kroh EM, Ruf IK, Pritchard CC, Gibson DF, et al. Argonaute2 complexes carry a population of circulating microRNAs independent of vesicles in human plasma. Proc Natl Acad Sci U S A (2011) 108(12):5003–8. doi:10.1073/pnas.1019055108
17. Vickers KC, Palmisano BT, Shoucri BM, Shamburek RD, Remaley AT. microRNAs are transported in plasma and delivered to recipient cells by high-density lipoproteins. Nat Cell Biol (2011) 13(4):423–33. doi:10.1038/ncb2210
21. Lawrie CH, Gal S, Dunlop HM, Pushkaran B, Liggins AP, Pulford K, et al. Detection of elevated levels of tumour-associated microRNAs in serum of patients with diffuse large B-cell lymphoma. Br J Haematol (2008) 141(5):672–5. doi:10.1111/j.1365-2141.2008.07077.x
22. Fayyad-Kazan H, Bitar N, Najar M, Lewalle P, Fayyad-Kazan M, Badran R, et al. Circulating miR-150 and miR-342 in plasma are novel potential biomarkers for acute myeloid leukemia. J Transl Med (2013) 11(1):31. doi:10.1186/1479-5876-11-31
23. Ferrajoli A, Shanafelt TD, Ivan C, Shimizu M, Rabe KG, Nouraee N, et al. Prognostic value of miR-155 in individuals with monoclonal B-cell lymphocytosis and patients with B chronic lymphocytic leukemia. Blood (2013) 122(11):1891–9. doi:10.1182/blood-2013-01-478222
24. Foss KM, Sima C, Ugolini D, Neri M, Allen KE, Weiss GJ. miR-1254 and miR-574-5p: serum-based microRNA biomarkers for early-stage non-small cell lung cancer. J Thorac Oncol (2011) 6(3):482–8. doi:10.1097/JTO.0b013e318208c785
26. Brase JC, Johannes M, Schlomm T, Fälth M, Haese A, Steuber T, et al. Circulating miRNAs are correlated with tumor progression in prostate cancer. Int J Cancer (2011) 128(3):608–16. doi:10.1002/ijc.25376
27. Bryant RJ, Pawlowski T, Catto JW, Marsden G, Vessella RL, Rhees B, et al. Changes in circulating microRNA levels associated with prostate cancer. Br J Cancer (2012) 106(4):768–74. doi:10.1038/bjc.2011.595
28. Srivastava A, Goldberger H, Dimtchev A, Ramalinga M, Chijioke J, Marian C, et al. microRNA profiling in prostate cancer-the diagnostic potential of urinary miR-205 and miR-214. PLoS One (2013) 8(10):e76994. doi:10.1371/journal.pone.0076994
29. Schultz NA, Dehlendorff C, Jensen BV, Bjerregaard JK, Nielsen KR, Bojesen SE, et al. microRNA biomarkers in whole blood for detection of pancreatic cancer. JAMA (2014) 311(4):392–404. doi:10.1001/jama.2013.284664
31. Liu AM, Yao TJ, Wang W, Wong KF, Lee NP, Fan ST, et al. Circulating miR-15b and miR-130b in serum as potential markers for detecting hepatocellular carcinoma: a retrospective cohort study. BMJ Open (2012) 2(2):e000825. doi:10.1136/bmjopen-2012-000825
32. Borel F, Konstantinova P, Jansen PL. Diagnostic and therapeutic potential of miRNA signatures in patients with hepatocellular carcinoma. J Hepatol (2012) 56(6):1371–83. doi:10.1016/j.jhep.2011.11.026
33. Abdalla MA, Haj-Ahmad Y. Promising candidate urinary microRNA biomarkers for the early detection of hepatocellular carcinoma among high-risk hepatitis C virus Egyptian patients. J Cancer (2012) 3:19. doi:10.7150/jca.3.19
34. Ayaz L, Görür A, Yaroglu HY, Ozcan C, Tamer L. Differential expression of microRNAs in plasma of patients with laryngeal squamous cell carcinoma: potential early-detection markers for laryngeal squamous cell carcinoma. J Cancer Res Clin Oncol (2013) 139(9):1499–506. doi:10.1007/s00432-013-1469-2
35. Faltejskova P, Bocanek O, Sachlova M, Svoboda M, Kiss I, Vyzula R, et al. Circulating miR-17-3p, miR-29a, miR-92a and miR-135b in serum: evidence against their usage as biomarkers in colorectal cancer. Cancer Biomark (2012) 12(4):199–204. doi:10.3233/CBM-130308
36. Wang J, Huang SK, Zhao M, Yang M, Zhong JL, Gu YY, et al. Identification of a circulating microRNA signature for colorectal cancer detection. PLoS One (2014) 9(4):e87451. doi:10.1371/journal.pone.0087451
37. Toiyama Y, Hur K, Tanaka K, Inoue Y, Kusunoki M, Boland CR, et al. Serum miR-200c is a novel prognostic and metastasis-predictive biomarker in patients with colorectal cancer. Ann Surg (2014) 259(4):735–43. doi:10.1097/SLA.0b013e3182a6909d
38. Tsujiura M, Komatsu S, Ichikawa D, Shiozaki A, Konishi H, Takeshita H, et al. Circulating miR-18a in plasma contributes to cancer detection and monitoring in patients with gastric cancer. Gastric Cancer (2014) 18:1–9. doi:10.1007/s10120-014-0363-1
39. Chen Q, Ge X, Zhang Y, Xia H, Yuan D, Tang Q, et al. Plasma miR-122 and miR-192 as potential novel biomarkers for the early detection of distant metastasis of gastric cancer. Oncol Rep (2014) 31(4):1863–70. doi:10.3892/or.2014.3004
41. Komatsu S, Ichikawa D, Takeshita H, Tsujiura M, Morimura R, Nagata H, et al. Circulating microRNAs in plasma of patients with oesophageal squamous cell carcinoma. Br J Cancer (2011) 105(1):104–11. doi:10.1038/bjc.2011.198
42. Kishimoto T, Eguchi H, Nagano H, Kobayashi S, Akita H, Hama N, et al. Plasma miR-21 is a novel diagnostic biomarker for biliary tract cancer. Cancer Sci (2013) 104(12):1626–31. doi:10.1111/cas.12300
43. Yu J, Wang Y, Dong R, Huang X, Ding S, Qiu H. Circulating microRNA-218 was reduced in cervical cancer and correlated with tumor invasion. J Cancer Res Clin Oncol (2012) 138(4):671–4. doi:10.1007/s00432-012-1147-9
44. Yu S, Liu Y, Wang J, Guo Z, Zhang Q, Yu F, et al. Circulating microRNA profiles as potential biomarkers for diagnosis of papillary thyroid carcinoma. J Clin Endocrinol Metab (2012) 97(6):2084–92. doi:10.1210/jc.2011-3059
45. Yang C, Wang C, Chen X, Chen S, Zhang Y, Zhi F, et al. Identification of seven serum microRNAs from a genome-wide serum microRNA expression profile as potential noninvasive biomarkers for malignant astrocytomas. Int J Cancer (2013) 132(1):116–27. doi:10.1002/ijc.27657
47. Chen W, Wang H, Chen H, Liu S, Lu H, Kong D, et al. Clinical significance and detection of microRNA-21 in serum of patients with diffuse large B-cell lymphoma in Chinese population. Eur J Haematol (2014) 92(5):407–12. doi:10.1111/ejh.12263
48. Moussay E, Wang K, Cho JH, van Moer K, Pierson S, Paggetti J, et al. microRNA as biomarkers and regulators in B-cell chronic lymphocytic leukemia. Proc Natl Acad Sci U S A (2011) 108(16):6573–8. doi:10.1073/pnas.1019557108
50. Chen X, Hu Z, Wang W, Ba Y, Ma L, Zhang C, et al. Identification of ten serum microRNAs from a genome-wide serum microRNA expression profile as novel noninvasive biomarkers for nonsmall cell lung cancer diagnosis. Int J Cancer (2012) 130(7):1620–8. doi:10.1002/ijc.26177
51. Ercole CJ, Lange PH, Mathisen M, Chiou RK, Reddy PK, Vessella RL. Prostatic specific antigen and prostatic acid phosphatase in the monitoring and staging of patients with prostatic cancer. J Urol (1987) 138(5):1181–4.
53. Mahn R, Heukamp LC, Rogenhofer S, von Ruecker A, Müller SC, Ellinger J. Circulating microRNAs (miRNA) in serum of patients with prostate cancer. Urology (2011) 77(5):1265.e9–16. doi:10.1016/j.urology.2011.01.020
54. Ogata-Kawata H, Izumiya M, Kurioka D, Honma Y, Yamada Y, Furuta K, et al. Circulating exosomal microRNAs as biomarkers of colon cancer. PLoS One (2014) 9(4):e92921. doi:10.1371/journal.pone.0092921
55. Zhu C, Ren C, Han J, Ding Y, Du J, Dai N, et al. A five-microRNA panel in plasma was identified as potential biomarker for early detection of gastric cancer. Br J Cancer (2014) 110(9):2291–9. doi:10.1038/bjc.2014.119
56. Zhao A, Li G, Péoc’h M, Genin C, Gigante M. Serum miR-210 as a novel biomarker for molecular diagnosis of clear cell renal cell carcinoma. Exp Mol Pathol (2013) 94(1):115–20. doi:10.1016/j.yexmp.2012.10.005
57. Carlsen AL, Joergensen MT, Knudsen S, de Muckadell OB, Heegaard NH. Cell-free plasma microRNA in pancreatic ductal adenocarcinoma and disease controls. Pancreas (2013) 42(7):1107–13. doi:10.1097/MPA.0b013e318296bb34
58. Lewis F, Maughan NJ, Smith V, Hillan K, Quirke P. Unlocking the archive-gene expression in paraffin-embedded tissue. J Pathol (2001) 195(1):66–71. doi:10.1002/1096-9896(200109)195:1<66::AID-PATH921>3.0.CO;2-F
59. Masuda N, Ohnishi T, Kawamoto S, Monden M, Okubo K. Analysis of chemical modification of RNA from formalin-fixed samples and optimization of molecular biology applications for such samples. Nucleic Acids Res (1999) 27(22):4436–43. doi:10.1093/nar/27.22.4436
60. Varnholt H, Drebber U, Schulze F, Wedemeyer I, Schirmacher P, Dienes HP, et al. microRNA gene expression profile of hepatitis C virus-associated hepatocellular carcinoma. Hepatology (2008) 47(4):1223–32. doi:10.1002/hep.22158
61. Xi Y, Nakajima G, Gavin E, Morris CG, Kudo K, Hayashi K, et al. Systematic analysis of microRNA expression of RNA extracted from fresh frozen and formalin-fixed paraffin-embedded samples. RNA (2007) 13(10):1668–74. doi:10.1261/rna.642907
62. Li J, Smyth P, Flavin R, Cahill S, Denning K, Aherne S, et al. Comparison of miRNA expression patterns using total RNA extracted from matched samples of formalin-fixed paraffin-embedded (FFPE) cells and snap frozen cells. BMC Biotechnol (2007) 7(1):36. doi:10.1186/1472-6750-7-36
63. McDermott AM, Miller N, Wall D, Martyn LM, Ball G, Sweeney KJ, et al. Identification and validation of oncologic miRNA biomarkers for luminal A-like breast cancer. PLoS One (2014) 9(1):e87032. doi:10.1371/journal.pone.0087032
64. Lowery AJ, Miller N, Devaney A, McNeill RE, Davoren PA, Lemetre C, et al. microRNA signatures predict oestrogen receptor, progesterone receptor and HER2/neu receptor status in breast cancer. Breast Cancer Res (2009) 11(3):R27. doi:10.1186/bcr2257
65. de Rinaldis E, Gazinska P, Mera A, Modrusan Z, Fedorowicz GM, Burford B, et al. Integrated genomic analysis of triple-negative breast cancers reveals novel microRNAs associated with clinical and molecular phenotypes and sheds light on the pathways they control. BMC Genomics (2013) 14(1):643. doi:10.1186/1471-2164-14-643
66. van Schooneveld E, Wildiers H, Vergote I, Vermeulen PB, Dirix LY, Van Laere SJ. Dysregulation of microRNAs in breast cancer and their potential role as prognostic and predictive biomarkers in patient management. Breast Cancer Res (2015) 17(1):21. doi:10.1186/s13058-015-0526-y
67. Youssef YM, White NM, Grigull J, Krizova A, Samy C, Mejia-Guerrero S, et al. Accurate molecular classification of kidney cancer subtypes using microRNA signature. Eur Urol (2011) 59(5):721–30. doi:10.1016/j.eururo.2011.01.004
68. Lee JH, Voortman J, Dingemans AM, Voeller DM, Pham T, Wang Y, et al. microRNA expression and clinical outcome of small cell lung cancer. PLoS One (2011) 6(6):e21300. doi:10.1371/journal.pone.0021300
69. Lebanony D, Benjamin H, Gilad S, Ezagouri M, Dov A, Ashkenazi K, et al. Diagnostic assay based on hsa-miR-205 expression distinguishes squamous from nonsquamous non-small-cell lung carcinoma. J Clin Oncol (2009) 27(12):2030–7. doi:10.1200/JCO.2008.19.4134
70. Lawrie CH, Soneji S, Marafioti T, Cooper CD, Palazzo S, Paterson JC, et al. Microrna expression distinguishes between germinal center B cell-like and activated B cell-like subtypes of diffuse large B cell lymphoma. Int J Cancer (2007) 121(5):1156–61. doi:10.1002/ijc.22800
71. Lim EL, Trinh DL, Scott DW, Chu A, Krzywinski M, Zhao Y, et al. Comprehensive miRNA sequence analysis reveals survival differences in diffuse large B-cell lymphoma patients. Genome Biol (2015) 16(1):18. doi:10.1186/s13059-014-0568-y
72. Laginestra MA, Piccaluga PP, Fuligni F, Rossi M, Agostinelli C, Righi S, et al. Pathogenetic and diagnostic significance of microRNA deregulation in peripheral T-cell lymphoma not otherwise specified. Blood Cancer J (2014) 4(11):259. doi:10.1038/bcj.2014.78
73. Liu C, Iqbal J, Teruya-Feldstein J, Shen Y, Dabrowska MJ, Dybkaer K, et al. microRNA expression profiling identifies molecular signatures associated with anaplastic large cell lymphoma. Blood (2013) 122(12):2083–92. doi:10.1182/blood-2012-08-447375
74. Lloyd-Jones D, Adams RJ, Brown TM, Carnethon M, Dai S, De Simone G, et al. Executive summary: heart disease and stroke statistics – 2010 update: a report from the American heart association. Circulation (2010) 121(7):948. doi:10.1161/CIRCULATIONAHA.109.192666
75. Blenkiron C, Goldstein LD, Thorne NP, Spiteri I, Chin SF, Dunning MJ, et al. microRNA expression profiling of human breast cancer identifies new markers of tumor subtype. Genome Biol (2007) 8(10):R214. doi:10.1186/gb-2007-8-10-r214
77. Gilad S, Lithwick-Yanai G, Barshack I, Benjamin S, Krivitsky I, Edmonston TB, et al. Classification of the four main types of lung cancer using a microRNA-based diagnostic assay. J Mol Diagn (2012) 14(5):510–7. doi:10.1016/j.jmoldx.2012.03.004
78. Jaffe ES, Harris NL, Stein H, Campo E, Pileri SA, Swerdlow SH. Introduction and Overview of the Classification of the Lymphoid Neoplasms. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues (2008). p. 157–66.
79. Pearson TA, Mensah GA, Alexander RW, Anderson JL, Cannon RO III, Criqui M, et al. Markers of inflammation and cardiovascular disease application to clinical and public health practice: a statement for healthcare professionals from the centers for disease control and prevention and the American Heart Association. Circulation (2003) 107(3):499–511. doi:10.1161/01.CIR.0000052939.59093.45
82. Tijsen AJ, Creemers EE, Moerland PD, de Windt LJ, van der Wal AC, Kok WE, et al. MiR423-5p as a circulating biomarker for heart failure. Circ Res (2010) 106(6):1035–9. doi:10.1161/CIRCRESAHA.110.218297
83. Fan KL, Zhang HF, Shen J, Zhang Q, Li XL. Circulating microRNAs levels in Chinese heart failure patients caused by dilated cardiomyopathy. Indian Heart J (2013) 65(1):12–6. doi:10.1016/j.ihj.2012.12.022
84. D’Alessandra Y, Devanna P, Limana F, Straino S, Di Carlo A, Brambilla PG, et al. Circulating microRNAs are new and sensitive biomarkers of myocardial infarction. Eur Heart J (2010) 31(22):2765–73. doi:10.1093/eurheartj/ehq167
86. Jaguszewski M, Osipova J, Ghadri JR, Napp LC, Widera C, Franke J, et al. A signature of circulating microRNAs differentiates Takotsubo cardiomyopathy from acute myocardial infarction. Eur Heart J (2014) 35(15):999–1006. doi:10.1093/eurheartj/eht392
87. Osipova J, Fischer DC, Dangwal S, Volkmann I, Widera C, Schwarz K, et al. Diabetes-associated microRNAs in pediatric patients with type 1 diabetes mellitus: a cross-sectional cohort study. J Clin Endocrinol Metab (2014) 99(9):E1661–5. doi:10.1210/jc.2013-3868
88. Peng H, Zhong M, Zhao W, Wang C, Zhang J, Liu X, et al. Urinary miR-29 correlates with albuminuria and carotid intima-media thickness in type 2 diabetes patients. PLoS One (2013) 8(12):e82607. doi:10.1371/journal.pone.0082607
89. Duan X, Zhan Q, Song B, Zeng S, Zhou J, Long Y, et al. Detection of platelet microRNA expression in patients with diabetes mellitus with or without ischemic stroke. J Diabetes Complications (2014) 28(5):705–10. doi:10.1016/j.jdiacomp.2014.04.012
91. Monteleone K, Selvaggi C, Cacciotti G, Falasca F, Mezzaroma I, D’Ettorre G, et al. microRNA-29 family expression and its relation to antiviral immune response and viro-immunological markers in HIV-1-infected patients. BMC Infect Dis (2015) 15(1):51. doi:10.1186/s12879-015-0768-4
94. Jansen C, Reiberger T, Huang J, Eischeid H, Schierwagen R, Mandorfer M, et al. Circulating miRNA-122 levels are associated with hepatic necroinflammation and portal hypertension in HIV/HCV coinfection. PLoS One (2015) 10(2):e0116768. doi:10.1371/journal.pone.0116768
95. Hanson EK, Lubenow H, Ballantyne J. Identification of forensically relevant body fluids using a panel of differentially expressed microRNAs. Anal Biochem (2009) 387(2):303–14. doi:10.1016/j.ab.2009.01.037
98. Kirschner MB, Kao SC, Edelman JJ, Armstrong NJ, Vallely MP, van Zandwijk N, et al. Haemolysis during sample preparation alters microRNA content of plasma. PLoS One (2011) 6(9):e24145. doi:10.1371/journal.pone.0024145
99. Song J, Bai Z, Han W, Zhang J, Meng H, Bi J, et al. Identification of suitable reference genes for qPCR analysis of serum microRNA in gastric cancer patients. Dig Dis Sci (2012) 57(4):897–904. doi:10.1007/s10620-011-1981-7
100. Sanders I, Holdenrieder S, Walgenbach-Brünagel G, von Ruecker A, Kristiansen G, Müller SC, et al. Evaluation of reference genes for the analysis of serum miRNA in patients with prostate cancer, bladder cancer and renal cell carcinoma. Int J Urol (2012) 19(11):1017–25. doi:10.1111/j.1442-2042.2012.03082.x
Keywords: micro-RNA, biomarkers, diagnosis
Citation: Faruq O and Vecchione A (2015) microRNA: diagnostic perspective. Front. Med. 2:51. doi: 10.3389/fmed.2015.00051
Received: 29 May 2015; Accepted: 17 July 2015;
Published: 03 August 2015
Edited by:Alfredo Fusco, Consiglio Nazionale delle Ricerche, Italy
Reviewed by:Giancarlo Troncone, Università di Napoli Federico II, Italy
Pier Paolo Piccaluga, Bologna University, Italy
Copyright: © 2015 Faruq and Vecchione. 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) or licensor 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: Andrea Vecchione, Department of Clinical and Molecular Medicine, Division of Pathology, Faculty of Medicine and Psychology, Ospedale Santo Andrea, University “La Sapienza”, Via di Grottarossa 1035-1039, Rome 00198, Italy, firstname.lastname@example.org