Impact Factor 4.566 | CiteScore 5.6
More on impact ›

SYSTEMATIC REVIEW article

Front. Physiol., 05 June 2018 | https://doi.org/10.3389/fphys.2018.00685

Blood-Derived microRNAs for Pancreatic Cancer Diagnosis: A Narrative Review and Meta-Analysis

Xiaodong Li1,2,3, Pujun Gao4, Yang Wang5 and Xiaocong Wang1,2,3*
  • 1Suzhou Institute of Biomedical Engineering and Technology, Chinese Academy of Sciences, Suzhou, China
  • 2University of Chinese Academy of Sciences, Beijing, China
  • 3Department of Echocardiography, The First Hospital of Jilin University, Changchun, China
  • 4Department of Hepatology, The First Hospital of Jilin University, Changchun, China
  • 5Department of Orthopedics, China-Japan Friendship Hospital, Changchun, China

microRNAs (miRNAs) have been reported to be aberrantly expressed in patients with pancreatic cancer. In present review we explored the biological roles of miRNAs in pancreatic cancer and their clinical value in diagnosis. In the systematic review, the potential value of miRNAs as biomarkers was investigated by reviewing the altered miRNA profiles reported in pancreatic cancer patients in 356 included studies. In the subsequent meta-analysis, we included 17 studies in early diagnosis of pancreatic cancer with a panel of altered miRNAs. The following results were obtained: pooled sensitivity of 0.88 (95% confidence interval [CI] 0.83–0.92), pooled specificity of 0.83 (95%CI 0.77–0.88), diagnostic odds ratio of 27 (95%CI 14–53), and area under the receiver operating characteristic curve of 0.90 (95%CI 0.88–0.93). To further explore the value of a single miRNA, the diagnostic value of miR-21 in PA was also demonstrated by the pooled sensitivity (0.90, 95% CI: 0.82–0.94), specificity (0.72, 95% CI: 0.57-0.83) as well as AUC (0.91 (95%CI 0.88–0.93). In conclusion, our findings suggest that aberrant miRNA expression in blood play an essential role in pancreatic cancer, and meta-analysis revealed blood-derived miRNAs as probable biomarkers for early diagnosis of pancreatic cancer.

Introduction

Pancreatic cancer is one of the most malignant gastrointestinal (GI) tumors and thus has a poor prognosis, with the mortality of this disease ranking fourth among cancer-related deaths (Real, 2003). Due to the lack of early clinical manifestations and occult onset, most patients are already in advanced stages when diagnosed with pancreatic cancer, showing aggressive growth and spreading of the tumor, and therefore cannot be surgically cured (Parikh and Lillemoe, 2015). In addition, pancreatic cancer tumors are typically resistant to radiotherapy and chemotherapy, resulting a lower 5-year survival rate and high mortality (Govindan and Goldenberg, 2015). Currently, the diagnosis of pancreatic cancer depends mainly on nonspecific tumor biomarkers. However, due to their non-specificity, patients cannot be promptly diagnosed and receive proper treatment, thus greatly reducing patients' survival rate (Schmidt, 2012). Therefore, the identification of new types of pancreatic cancer biomarkers is essential for clinicians to improve the survival of pancreatic cancer patients.

microRNAs (miRNAs) are a class of single-stranded non-coding RNAs that are involved in the regulation of physical and pathological processes such as cell proliferation, protein metabolism, and tumor development. They are highly conserved and tissue-specific. Through binding to the 3′-untranslational region (UTR) of target mRNAs, miRNAs degrade or inhibit the translation of mRNA, a process known as post-transcriptional silencing, and participate in the regulation of target gene functions (Liu, 2014). In recent years, miRNAs have been reported to be associated with tumorigenesis of blood cancers and solid tumors (Garzon et al., 2015). In pancreatic cancer, the up-regulation or down-regulation of miRNAs is closely related to the biological characteristics of the tumor as well as tumor metastasis and prognosis (Ren et al., 2012).

We conducted the present review of relevant qualitative and quantitative studies to identify altered miRNA regulation with previous findings on patients with pancreatic cancer. This was followed by a meta-analysis to evaluate the early diagnostic value with altered miRNA profiles for pancreatic cancer.

Materials and Methods

Literature Search Strategy

A comprehensive literature search was carried out for studies reporting the association between circulating miRNAs and pancreatic cancer in patients through the following databases: PubMed, Embase, the Cochrane Library, and Web of Science. In addition, we searched the Chinese databases including Chinese National Knowledge Infrastructure (CNKI) database, Technology of Chongqing VIP database, and Wan Fang Data. We used search terms with the key words: “pancreatic cancer” “pancreatic ductal adenocarcinoma,” “pancreatic neoplasm” “pancreatic tumor” “pancreatic carcinoma,” “microRNA,” “miRNA,” “diagnosis,” “specificity,” “sensitivity,” and “ROC curve” up to February 1, 2018. In addition, we searched conference abstracts, summaries and references of reviews to find any potentially eligible articles.

Inclusion Criteria

In the narrative review, we included quantitative and qualitative studies investigating the correlation between miRNA expression and pancreatic cancer, including reviews, letters, reports, editorials, research articles, or conference abstracts.

In the meta-analysis, included studies had to meet the following criteria: (1) randomized case-control study on patients with pancreatic cancer, (2) research on the association between circulating miRNAs and pancreatic cancer, and (3) provided sufficient data that could be calculated or extracted from the article.

The exclusion criteria were: animal model research, reviews, commentaries, editorials, or duplicate publications, unrelated to pancreatic cancer and miRNAs, provided limited data, or overlap of patient selection with another study.

Data Extraction and Quality Assessment

The following data were extracted by two of the authors independently from the full text of eligible articles: first author's name; year and country of publication; sample size, sex, and miRNA expression signatures; and specificity and sensitity values of tested miRNAs. The quality of the included studies was systematically evaluated according to QUADAS-2 guidelines for the qualitative assessment of diagnostic accuracy studies (Whiting et al., 2006; Kojimahara et al., 2014).

Statistical Analysis of Meta-Analysis

Stata statistical software and Meta-DiSc 1.4 were used for data analyses. The true positive (TP), false positive (FP), true negative (TN), and false negative (FN) rates were calculated for the obtained data. Heterogeneity across studies was assessed based on the χ2-based Cochran's Q test and Higgins' I2 statistics. The bivariate binomial mixed model was used to calculate the pooled sensitivity, specificity, diagnostic odds ratio (DOR), positive likelihood ratio (PLR), and negative likelihood ratio (NLR) with 95% confidence intervals (CIs). A summary receiver operating characteristic curve (SROC) was constructed based on the pooled sensitivity and specificity. The area under the SROC curve (AUC) provided the accuracy of a quantitative diagnostic test with miRNAs for pancreatic cancer. In addition, to explore the potential heterogeneity among included studies, subgroup analyses and meta-regression were performed. Deek's funnel plots were adopted to examine publication bias across studies. All statistical tests were two-sided with significance level set as p < 0.05.

Results

Narrative Review: Relationship Between miRNA Expression and Pancreatic Cancer

Altered Expression of miRNAs in Pancreatic Cancer

miRNAs regulate target gene expression, and their expression in cancer tissues and normal tissues can differ significantly. In oncology, miRNAs are now regarded as oncogenes or tumor suppressor genes. It is generally believed that miRNAs that are up-regulated in tumor tissue are oncogenes that promote tumor development by regulating cell differentiation or apoptosis via inhibiting tumor suppressor genes. Bloomston et al. using miRNA chips and real-time PCR identified seven miRNAs (miR-21, miR-221, miR-222, miR-181a, miR-181b, miR-181d, and miR-155) that were up-regulated in pancreatic cancer tissues (Bloomston et al., 2007). Additionally, Volinia et al. aanalyzed pancreatic tumors in a large number of patients through RNA-seq technology and found miRNAs that were expressed at higher levels in tumors (miR-17-5p, miR-20a, miR-21, miR-92, miR-106a, and miR-155) (Volinia et al., 2006).

Some miRNAs are also downregulated in pancreatic cancers where they regulate tumor suppressor genes; for example, miR-34 was shown to be down-regulated in pancreatic cancer cell lines. Ji et al. found that miR-34a expression in at least two pancreatic cancer cell lines was reduced by at least 2 fold, and in 11 pancreatic cancer cell lines, miR-34a expression was even reduced by more than 10 fold (Ji et al., 2009). In addition, Lodygin et al. found that miR-34 expression in the MiaPaCa-2 and Bxpc-3 pancreatic cancer cell lines was extremely reduced (Lodygin et al., 2008). Saito et al. also found that miR-127 is down-regulated in human primary tumors compared to levels in normal cells, suggesting that miR-127 may be a potential tumor suppressor (Saito et al., 2006). Moreover, by comparing the expression levels of 241 miRNAs in 60 types of tumor cells and normal tissues from the National Cancer Institute (NCI), Gaur et al. found that most miRNAs were down-regulated in tumor cells, suggesting that most of the miRNAs may be tumor suppressors (Gaur et al., 2007). miRNA profiles in identifying pancreatic cancer and other pancreatic diseases. Some studies suggest that miR-204 is mainly expressed in insulinoma-regulating insulin secretion. Ki-67 is a marker of cell proliferation and has been linked to prognosis in many oncology studies. Up-regulation of miR-21 is associated with higher Ki-67 expression and hepatic metastasis, suggesting that miRNA changes are associated with pancreatic endocrine tumors, adenoma transformation, and malignant tumor progression. Roldo et al. screened miRNA profiles in 12 non-pancreatic tumor tissues and primary pancreatic tumors (insulinomas, non-functioning pancreatic endocrine tumors, and adenocarcinomas) and found miRNA expression patterns that differed from those in normal pancreatic tissue. Ren et al. examined the expression of 95 miRNAs involved in oncogenesis in pancreatic cancer tissues and compared miRNA signatures in normal human pancreatic ductal epithelial (HPDE) cells and normal pancreatic tissues. They found that 8 miRNAs (miR-196a, miR-190, miR-186, miR-221, miR-222, miR-200b, miR-15b, and miR-95) were abundant in pancreatic cancer tissues (Ren et al., 2012). These authors concluded that pancreatic cancer tissue or cell lines have unique miRNA expression profiles. Bloomston et al. used miRNA microarrays to investigate the expression of 326 miRNAs in 65 cases of pancreatic cancer, 42 cases of chronic pancreatitis, and normal pancreas tissue, and the results showed that compared with their expression in normal pancreatic tissue, 21 miRNAs were up-regulated and four miRNAs were down-regulated in pancreatic cancers (Bloomston et al., 2007). Fifteen miRNAs were up-regulated and eight miRNAs were down-regulated in pancreatic cancer compared with chronic pancreatitis. The expression profiles of these miRNAs were used to distinguish chronic pancreatitis and pancreatic cancer with accuracy of 93%. Subsequent cluster analysis found that miRNA expression patterns were very similar between chronic pancreatitis and normal pancreas, whereas miRNA expression was significantly different between chronic pancreatitis or normal pancreas. Therefore, miRNA expression of pancreatic cancer could be used for differential diagnosis of pancreatic cancer from benign diseases.

miRNA Profiles in Identifying Pancreatic Cancer and Other Tumors

miRNA expression is strongly tissue-specific. Volinia et al. used miRNA microarray technology to examine 363 tissue samples of six types of tumors from pancreas, lung, breast, stomach, prostate, and colon, and the results revealed that the expression profile of a cluster of 137 miRNAs can be a good indicator for differentiating the source of tumor tissue (Volinia et al., 2006). A 4-year study found that different tumors have specific miRNA expression patterns, including chronic lymphocytic leukemia, gastric cancer, lung cancer, breast cancer, prostate cancer, pancreatic cancer, liver cancer, and thyroid cancer. In pancreatic tissues, up-regulation of miR-216 and miR-217 expression as well as deletion of miR-133a can be regarded as features of pancreatic tissues to determine the pancreatic origin of tissues or cells (Gironella et al., 2007).

Meta-Analysis: Diagnostic Value of miRNA Profile for Pancreatic Cancer Diagnosis

We identified 17 publications examining the clinical value of miRNA expression for the diagnosis of pancreatic cancer. The details of the selection process are presented in Figure 1. A total of 939 cases of pancreatic cancer and 977 control cases were included for the meta-analysis across 17 studies, and the study characteristics along with the QUADAS scores of the included studies are presented in Table 1. All patients with pancreatic cancer were diagnosed according to clinically recognized diagnostic criteria. Analysis of the quality of each study revealed QUADAS scores ranging from 4 to 9.

FIGURE 1
www.frontiersin.org

Figure 1. Process of study selection.

TABLE 1
www.frontiersin.org

Table 1. Summary of included studies.

The heterogeneity I2 values for inter-study variability were 85% (sensitivity) and 78.05% (specificity). The Spearman correlation coefficient of 0.49 (p = 0.061) also suggested there was no heterogeneity due to the threshold effect (Figure 2).

FIGURE 2
www.frontiersin.org

Figure 2. Forrest plot of estimates of sensitivity and specificity.

In this meta-analysis, the summary assessment of miRNAs in the diagnosis of pancreatic cancer showed that the pooled sensitivity was 0.88 (95%CI 0.83–0.92) and the pooled specificity was 0.83 (95%CI 0.77–0.88). The DOR was 36.7 (95%CI 18.75–71.80; Figure 3). The area under the SROC was 0.92 (95%CI 0.90–0.94; Figure 4). The PLR was 4.3 (95%CI 3.1–6.0), and the NLR was 0.16 (95%CI 0.11–0.24), as shown in the Fagan's nomogram in Figure 5.

FIGURE 3
www.frontiersin.org

Figure 3. Forrest plot of estimates of DOR.

FIGURE 4
www.frontiersin.org

Figure 4. Summary receiver operating characteristic (SROC) curve.

FIGURE 5
www.frontiersin.org

Figure 5. Fagan's Nomogram for assessment of post-test probabilities.

A subgroup analysis of heterogeneity sources revealed that there were no significant difference in sample size, ethnicity, or number of miRNA detected. The use of circulating miRNAs for diagnosing pancreatic cancer had a sensitivity and specificity of 0.80 and 0.89, respectively (Figure 6).

FIGURE 6
www.frontiersin.org

Figure 6. Forrest plots from multivariable meta-regression and subgroup analyses for sensitivity and specificity.

To further explore the diagnostic value of a single miRNA in pancreatic cancer diagnosis, we found that there were four studies focusing on miR-21 with data available. Our meta analysis on single miR-21 indicated that the pooled sensitivity was 0.90 (95%CI 0.82–0.94) and the pooled specificity was 0.72 (95%CI 0.57–0.83). The area under the SROC was 0.91 (95%CI 0.88–0.93; Figure 7). Those findings suggest that a single miR-21 can be a good indicator for pancreatic cancer diagnosis.

FIGURE 7
www.frontiersin.org

Figure 7. Diagnostic value of miR-21 on pancreatic cancer. (A) Forrest plot of estimates of sensitivity and specificity (B) Summary receiver operating characteristic (SROC) curve.

To explore any potential publication bias of the studies included in this meta-analysis, the Deek's funnel plot with the asymmetry test was generated, and the p value was 0.7, suggesting no publication bias existed in the included studies (Figure 8).

FIGURE 8
www.frontiersin.org

Figure 8. Deek's funnel plot for the assessment of publication bias.

Discussion

At present, the diagnosis of malignant tumors depends mostly on medical imaging, but the associated sensitivity and specificity are poor, leading to tumors not being diagnosed in the early stage of cancer. As a result, most patients with malignant tumors are diagnosed in a later stage. With a continually increasing mortality rate, pancreatic cancer has become a health and economic burden for patients and their family members. Therefore, there is an urgent need to find more sensitive, non-invasive biomarkers to facilitate the diagnosis of pancreatic cancer (Goh and Yoon, 2012).

miRNAs are involved in the development and progression of various diseases, especially malignant tumors. Some studies have confirmed that miRNAs can be stable in bodily fluids for cancer detection. In the development of the pancreas and the onset of pancreatic neoplasm, miRNAs are important regulators and mediators. Adopting specific miRNAs as biomarkers for early diagnosis of pancreatic cancer has potential implications for clinicians and patients.

In this review, 17 eligible articles with a total of 1916 cases were identified through database and manual searches and included in a meta-analysis. According to QUADAS-2 quality evaluation, all the included studies were of middle-to-high quality. Meta-analysis showed that the combined sensitivity, specificity, and DOR for the miRNA profiles in the 17 studies were 88%, 83%, and 36.7, respectively. The PLR and NLR were 4.3 and 0.16, respectively. The PLR suggests that a patient with pancreatic cancer is 4.3 times more likely to have positive results on miRNA tests than a normal person and the NLR suggests that the probability of a false negative result basted on miRNA signature detection was 16%. Additionally, the AUC of the combined ROC curve for circulating miRNAs in diagnosing pancreatic cancer was 0.92, suggesting that the circulating miRNA profile is of intermediate efficacy for the diagnosis of pancreatic cancer. A subgroup analysis of sources of heterogeneity revealed that there were no significant differences the sample size and patient ethnicity among the included studies. Therefore, the results of this quantitive study indicate that the circulating miRNA signature has sufficient accuracy for the diagnosis of pancreatic cancer.

To further explore the value of a single miRNA in pancreatic cancer diagnosis, miR-21 was examined. The previous evidences also suggested that miR-21 and itsdownstream targets play a key role in cell proliferation, apoptosis and cell cycle and mediate oncogenic function in pancreatic cancer (Park et al., 2009; Bhatti et al., 2011). The results of meta analysis indicate that the diagnostic value of of miR-21 was relatively higher than a panel of miRNAs. According to these data, the circulating miR-21 may be a promising diagnostic biomarker for diagnosing pancreatic cancer.

There are some limitations in this study. First, the limited number of patients and controls may affect the results of meta-analysis. Some studies were excluded due to the lack of sufficient data collected during the screening process. Secondly, the purpose of this study was to investigate the effectiveness of the circulating miRNA signature as a biomarker of pancreatic cancer, but samples for other types of cancer may affect the interpretation of the results of the meta-analysis. Finally, in the included studies, the differences in the duration of sample storage, miRNA extraction methods, and miRNA detection methods could influence the results of the meta-analysis. The miRNA transcript levels were affected by the different RNA processing methods. Moreover, the studies utilized different methods for quantitative detection and normalization in miRNA analysis, which may account for the differences reported across different studies.

Adopting a proper miRNA signature for individual diagnosis in clinical practice is still a great challenge. Further studies are needed for validation, even though the results in the current analysis showed that the miRNA expression profile can be used as a diagnostic indicator of pancreatic cancer. Moreover, miRNAs provide new targets and indicators for developing cancer therapies and predicating prognosis of pancreatic cancer, which is of great significance to improving the survival of patients and increasing the expected life expectancy and quality of life of patients with pancreatic cancer.

In conclusion, the present meta-analysis confirms a potential role for miRNA detection in pancreatic cancer diagnosis. Moreover, further studies are required to confirm molecular mechanism of the dysregulated circulating miRNA signature in pancreatic cancer, and prospective, multi-centered, large-scale clinical trials will further aid the establishment of miRNA combinations as diagnostic biomarkers for pancreatic cancer and elucidate the pathophysiological interactions between miRNAs and pancreatic pathology (Firpo et al., 2014).

Author Contributions

XL and PG did the literature research, data acquisition, statistical analysis, and wrote the manuscript. YW provided insightful thoughts to study concepts and wrote the manuscript. XW designed the study, revised the manuscript, and approved the final version.

Funding

This work was supported by the ninth academy youth fund of the First Hospital of Jilin University (grant no. JDYY92018024).

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.

References

Abue, M., Yokoyama, M., Shibuya, R., Tamai, K., Yamaguchi, K., Sato, I., et al. (2015). Circulating miR-483-3p and miR-21 is highly expressed in plasma of pancreatic cancer. Int. J. Oncol. 46, 539–547. doi: 10.3892/ijo.2014.2743

PubMed Abstract | CrossRef Full Text | Google Scholar

Alemar, B., Izetti, P., Gregório, C., Macedo, G. S., Castro, M. A., Osvaldt, A. B., et al. (2016). miRNA-21 and miRNA-34a are potential minimally invasive biomarkers for the diagnosis of pancreatic ductal adenocarcinoma. Pancreas 45, 84–92. doi: 10.1097/MPA.0000000000000383

PubMed Abstract | CrossRef Full Text | Google Scholar

Bhatti, I., James, V., Hall, R. I., Lund, J. N., Tufarelli, C., Lobo, D. N., et al. (2011). Knockdown of microRNA-21 inhibits proliferation and increases cell death by targeting programmed cell death 4 (PDCD4) in pancreatic ductal adenocarcinoma. Soc. Surg. Aliment. Tract. 15, 199–208. doi: 10.1007/s11605-010-1381-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Bloomston, M., Frankel, W. L., Petrocca, F., Volinia, S., Alder, H., Hagan, J. P., et al. (2007). MicroRNA expression patterns to differentiate pancreatic adenocarcinoma from normal pancreas and chronic pancreatitis. JAMA 297, 1901–1908. doi: 10.1001/jama.297.17.1901

PubMed Abstract | CrossRef Full Text | Google Scholar

Cote, G. A., Gore, A. J., McElyea, S. D., Heathers, L. E., Xu, H., Sherman, S., et al. (2014). A pilot study to develop a diagnostic test for pancreatic ductal adenocarcinoma based on differential expression of select miRNA in plasma and bile. Am. J. Gastroenterol. 109, 1942. doi: 10.1038/ajg.2014.331

PubMed Abstract | CrossRef Full Text | Google Scholar

Firpo, M. A., Boucher, K. M., and Mulvihill, S. J. (2014). Prospects for developing an accurate diagnostic biomarker panel for low prevalence cancers. Theor. Biol. Med. Model. 11, 34. doi: 10.1186/1742-4682-11-34

PubMed Abstract | CrossRef Full Text | Google Scholar

Garzon, R., Calin, G. A., and Croce, C. M. (2015). MicroRNAs in cancer. Annu. Rev. Med. 60, 167–179. doi: 10.1146/annurev.med.59.053006.104707

PubMed Abstract | CrossRef Full Text | Google Scholar

Gaur, A., Jewell, D. A., Liang, Y., Ridzon, D., Moore, J. H., Chen, C., et al. (2007). Characterization of microrna expression levels and their biological correlates in human cancer cell lines. Cancer Res. 67, 2456–2468. doi: 10.1158/0008-5472.CAN-06-2698

PubMed Abstract | CrossRef Full Text | Google Scholar

Gironella, M., Seux, M., Xie, M. J., Cano, C., Tomasini, R., Gommeaux, J., et al. (2007). Tumor protein 53-induced nuclear protein 1 expression is repressed by miR-155, and its restoration inhibits pancreatic tumor development. Proc. Natl. Acad. Sci. U.S.A. 104, 16170–16175. doi: 10.1073/pnas.0703942104

PubMed Abstract | CrossRef Full Text | Google Scholar

Goh, K. L., and Yoon, B. K. (2012). Early detection of pancreatic cancer: a possibility in some cases but not a reality in most. J. Dig. Dis. 13, 389–392. doi: 10.1111/j.1751-2980.2012.00609.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Govindan, S. V., and Goldenberg, D. M. (2015). Combining Radioimmunotherapy and Antibody-Drug Conjugates for Improved Cancer Therapy. US. Patent No 9,272,057. Washington, DC: U.S. Patent and Trademark Office.

Google Scholar

Hu, Y., Zhang, H., and Shi, W.ei, Tang, J. (2015). The diagnostic value of plasma miR-210 combined with serum tumor markers for pancreatic cancer. World Chin. J. Digestion 147–152. doi: 10.11569/wcjd.v23.i1.147

CrossRef Full Text

Ji, Q., Hao, X., Zhang, M., Tang, W., Yang, M., Li, L., et al. (2009). MicroRNA miR-34 inhibits human pancreatic cancer tumor-initiating cells. PLoS ONE 4:e6816. doi: 10.1371/journal.pone.0006816

PubMed Abstract | CrossRef Full Text | Google Scholar

Kojimahara, N., Morizane, T., Nakayama, T., Fukuoka, T., Kawai, F., Sato, Y., et al. (2014). Utilization of QUADAS-2; a revised tool for the quality assessment of diagnostic accuracy studies 2 as a risk of bias evaluation tool. Jpn Pharmacol. Ther. 42, s127–s134. doi: 10.7543/j.issn.1006-9674.2013.03.004

CrossRef Full Text

Komatsu, S., Ichikawa, D., Miyamae, M., Kawaguchi, T., Moriumura, R., Hirajima, S., et al. (2015). Malignant potential in pancreatic neoplasm; new insights provided by circulating miR-223 in plasma. Expert Opin. Biol. Ther. 221, 773–785. doi: 10.1517/14712598.2015.1029914

CrossRef Full Text | Google Scholar

Li, A., Yu, J., Kim, H., Wolfgang, C. L., Canto, M. I., Hruban, R. H., et al. (2013). MicroRNA array analysis finds elevated serum miR-1290 accurately distinguishes patients with low-stage pancreatic cancer from healthy and disease controls. Clin. Cancer Res. 19, 3600–3610. doi: 10.1158/1078-0432.CCR-12-3092

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, J., Gao, J., Du, Y., Li, Z., Ren, Y., Gu, J., et al. (2012). Combination of plasma microRNAs with serum CA19-9 for early detection of pancreatic cancer. Int. J. Cancer 131, 683–691. doi: 10.1002/ijc.26422

PubMed Abstract | CrossRef Full Text | Google Scholar

Liu, J., Gao, J., Li, Z., Ren, Y., Wang, X., Wang, W., et al. (2011). Detection of plasma miR-155 in patients with pancreatic cancer and its diagnostic value. Chin. J. Pancreatol. 11, 79–81. doi: 10.3760/cma.j.issn.1674-1935.2011.02.001

CrossRef Full Text

Liu, Y. W. (2014). MicroRNAs: genomics, biogenesis, mechanism, and function. Biosensors 58, 388. doi: 10.1016/j.bio.2014.02.082

CrossRef Full Text

Lodygin, D., Tarasov, V., Epanchintsev, A., Berking, C., Knyazeva, T., Körner, H., et al. (2008). Inactivation of miR-34a by aberrant CpG methylation in multiple types of cancer. Cell Cycle 7, 2591-2600. doi: 10.4161/cc.7.16.6533

PubMed Abstract | CrossRef Full Text | Google Scholar

Miyamae, M., Komatsu, S., Ichikawa, D., Kawaguchi, T., Hirajima, S., Okajima, W., et al. (2015). Plasma microRNA profiles: identification of miR-744 as a novel diagnostic and prognostic biomarker in pancreatic cancer. Br. J. Cancer 113, 1467–1476. doi: 10.1038/bjc.2015.366

PubMed Abstract | CrossRef Full Text | Google Scholar

Morimura, R., Komatsu, S., Ichikawa, D., Takeshita, H., Tsujiura, M., Nagata, H., et al. (2011). Novel diagnostic value of circulating miR-18a in plasma of patients with pancreatic cancer. Br. J. Cancer 105, 1733–1740. doi: 10.1038/bjc.2011.453

PubMed Abstract | CrossRef Full Text | Google Scholar

Pan, F., Wen, Y., Ma, S., Cao, W., Dong, J., Zhao, Y., et al. (2012). Correlation between plasma miRNA expression profile and pancreatic cancer. J. Nanjing Med. Univ. 32, 1541–1544.

Pan, W. (2014). Study of Plasma miRNAs Related to the Diagnosis of Pancreatic Cancer. Jinan: Shandong University.

Parikh, P. Y., and Lillemoe, K. D. (2015). Surgical management of pancreatic cancer–distal pancreatectomy. Semin. Oncol. 42, 110–122. doi: 10.1053/j.seminoncol.2014.12.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Park, J. K., Lee, E. J., Esau, C., and Schmittgen, T. D. (2009). Antisense inhibition of microRNA-21 or−221 arrests cell cycle, induces apoptosis, and sensitizes the effects of gemcitabine in pancreatic adenocarcinoma. Pancreas 38, e190–e199. doi: 10.1097/MPA.0b013e3181ba82e1

PubMed Abstract | CrossRef Full Text | Google Scholar

Que, R., Ding, G., Chen, J., and Cao, L. (2013). Analysis of serum exosomal microRNAs and clinicopathologic features of patients with pancreatic adenocarcinoma. World J. Surg. Oncol. 11, 1–9. doi: 10.1186/1477-7819-11-219

PubMed Abstract | CrossRef Full Text | Google Scholar

Real, F. X. (2003). A “catastrophic hypothesis” for pancreas cancer progression. Gastroenterology 124, 1958–1964. doi: 10.1016/S0016-5085(03)00389-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Ren, Y., Gao, J., Liu, J. Q., Wang, X. W., Gu, J. J., Huang, H. J., et al. (2012). Differential signature of fecal microRNAs in patients with pancreatic cancer. Mol. Med. Rep. 6, 201–209. doi: 10.3892/mmr.2012.862

PubMed Abstract | CrossRef Full Text | Google Scholar

Saito, Y., Liang, G., Egger, G., Friedman, J. M., Chuang, J. C., Coetzee, G. A., et al. (2006). Specific activation of microRNA-127 with downregulation of the proto-oncogene BCL6 by chromatin-modifying drugs in human cancer cells. Cancer Cell 9, 435–443. doi: 10.1016/j.ccr.2006.04.020

PubMed Abstract | CrossRef Full Text | Google Scholar

Schmidt, C. (2012). Early detection tools for pancreatic cancer. J. Natl. Cancer Inst. 104, 1117. doi: 10.1093/jnci/djs348

PubMed Abstract | CrossRef Full Text | Google Scholar

Schultz, N. A., Dehlendorff, C., Jensen, B. V., Bjerregaard, J. K., Nielsen, K. R., Bojesen, S. E., et al. (2014). MicroRNA biomarkers in whole blood for detection of pancreatic cancer. J. Am. Med. Assoc. 311, 392-404. doi: 10.1001/jama.2013.284664

PubMed Abstract | CrossRef Full Text | Google Scholar

Shi, W. (2014). Aberrant Expression of miR-155 and miR-196a in the Diagnosis of Pancreatic Cancer. Kunming: Kunming Medical University.

Volinia, S., Calin, G. A., Liu, C. G., Ambs, S., Cimmino, A., Petrocca, F., et al. (2006). A microRNA expression signature of human solid tumors defines cancer gene targets. Proc. Natl. Acad. Sci. U.S.A. 103, 2257–2261. doi: 10.1073/pnas.0510565103

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, J., Chen, J., Chang, P., Leblanc, A., Li, D., Abbruzzesse, J. L., et al. (2009). MicroRNAs in plasma of pancreatic ductal adenocarcinoma patients as novel blood-based biomarkers of disease. Cancer Prev. Res. 2, 807-813. doi: 10.1158/1940-6207.CAPR-09-0094

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, S., Liu, J., Lei, K., and Jia, S. (2015). Aberrant overexpressions of microRNAs in plasma and their correlations with the clinical features of patients with pancreatic cancer. Tumor 35, 905–910. doi: 10.3781/j.issn.1000-7431.2015.33.123

CrossRef Full Text | Google Scholar

Whiting, P. F., Weswood, M. E., Rutjes, A. W., Reitsma, J. B., Bossuyt, P. N., and Kleijnen, J. (2006). Evaluation of QUADAS, a tool for the quality assessment of diagnostic accuracy studies. BMC Med. Res. Methodol. 6:9. doi: 10.1186/1471-2288-6-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Keywords: microRNAs, pancreatic cancer, diagnosis, differential, blood, meta-analysis

Citation: Li X, Gao P, Wang Y and Wang X (2018) Blood-Derived microRNAs for Pancreatic Cancer Diagnosis: A Narrative Review and Meta-Analysis. Front. Physiol. 9:685. doi: 10.3389/fphys.2018.00685

Received: 20 March 2018; Accepted: 16 May 2018;
Published: 05 June 2018.

Edited by:

Atsushi Masamune, Tohoku University, Japan

Reviewed by:

Rei Suzuki, Fukushima Medical University, Japan
Kenji Takahashi, Asahikawa Medical University, Japan

Copyright © 2018 Li, Gao, Wang and Wang. 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 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: Xiaocong Wang, xiaocwang163@163.com