Background
Lung cancer is the leading cause of cancer deaths worldwide, and non-small cell lung cancer (NSCLC) accounts for nearly 85 % of all cases [
1]. Despite recent advances in experimental and clinical oncology, NSCLC is mostly diagnosed in late stages and survival has not improved significantly over several decades. To date, mechanisms underlying NSCLC carcinogenesis and progression remain poorly understood. Therefore, it is urgent to elucidate the regulatory network underlying NSCLC and develop novel biomarkers for its early diagnosis, accurate assessment, targeted therapy, and prognosis evaluation.
MicroRNAs (miRNAs) are short (about 22 nucleotides in length), highly conserved small non-coding RNA molecules that negatively regulate gene expression by binding to target messenger RNAs (mRNAs) at their 3′-untranslated region, leading to mRNA degradation or translation suppression [
2]. Deregulation of miRNA expression has been identified in many human diseases, including cancers. Some highly expressed miRNAs could function as oncogenes by repressing tumor suppressor genes, whereas low-expressed miRNAs could function as tumor suppressors by negatively regulating oncogenes. Emerging evidence suggests that miRNAs act as key regulators in a wide variety of biological processes that contribute to tumorigenesis and development, such as tumor cell differentiation, proliferation, apoptosis, invasion, angiogenesis, and epithelial mesenchymal transition [
3‐
5]. Since circulating miRNAs are well protected from RNase digestions and highly stable in plasma/serum [
6], they have been regarded as novel potential biomarkers in cancer detection and monitoring. For example, serum miR-30e and miR-223 are useful diagnostic biomarkers for hepatocellular carcinoma [
7]. Serum miR-200c expression correlates with overall survival of patients with gastric cancer [
8]. Serum expression levels of miR-17, miR-21, and miR-92 predict recurrence after adjuvant chemotherapy in colon cancer patients [
9]. Serum miR-183 can be used to predict the response of renal cell carcinoma cells to the cytotoxicity induced by natural killer cells [
10]. However, the use of circulating miRNAs as blood-based, minimally invasive biomarkers in NSCLC is still relatively less explored.
miR-195 is located at chromosome 17p13.1, a region that is frequently deleted in human cancers. Extensive researches have suggested decreased miRNA-195 expression and its tumor suppressive function in various solid tumors, including glioblastoma [
11], thyroid cancer [
12], tongue squamous cell carcinoma [
13], esophageal squamous cell carcinoma [
14], gastric cancer [
15], colorectal cancer [
16], hepatocellular carcinoma [
17], prostate cancer [
18], cervical cancer [
19], bladder cancer [
20], and osteosarcoma [
21]. Circulating miR-195 has been identified as a potential marker for the detection and/or prognosis evaluation of adrenocortical cancer [
22], breast cancer [
23], cervical cancer [
24], and osteosarcoma [
25]. In patients with NSCLC, tissue miRNA-195 expression was downregulated, and its downregulation was correlated with shorter overall survival [
26]. However, the diagnostic and prognostic value of plasma miRNA-195 in NSCLC patients remains unknown. In the present study, we investigated plasma miRNA-195 levels in patients with NSCLC and evaluated its association with clinicopathological features and survival time.
Discussion
Up to now, the exact mechanisms underlying NSCLC are not fully understood. The discovery of miRNAs has broadened our understanding of carcinogenesis. In terms of NSCLC, abnormal expression of several miRNAs and their function has been reported. For example, miRNA-1290 showed increased expression in NSCLC tissues, and its upregulation was correlated with positive lymph node metastasis and advanced clinical stage [
28]. Low expression of miRNA-345 and miRNA-34a predicted shorter overall survival of NSCLC patients [
29,
30]. Decreased serum miRNA-499 may serve as a novel diagnostic biomarker for NSCLC [
31]. Ectopic expression of miRNA-124 reduced lung cancer cell proliferation, invasion, and migration [
32]. Thus, functional miRNAs may be applied for NSCLC diagnosis and prognosis and also act as potential novel therapeutic targets.
Although many miRNAs are expressed in tissues and tumor cells, their development as biomarkers requires tissue collection by invasive methods as opposed to the more convenient approach of studying peripheral blood. The stability and easy detectability make circulating miRNAs an ideal candidate to serve as a biomarker for cancer detection. In this study, we showed decreased plasma miRNA-195 levels in NSCLC patients compared with healthy controls. Downregulation of plasma miRNA-195 was correlated with lymphatic metastasis and advanced TNM stage. ROC curve analysis revealed that plasma miRNA-195 had a moderate diagnostic value for NSCLC. Moreover, multivariate analysis confirmed plasma miRNA-195 expression as an independent prognostic factor for NSCLC patients. These results suggest that plasma miRNA-195 may serve as a useful diagnostic and prognostic biomarker for NSCLC.
Our results are consistent with previous findings. Zhang et al. identified circulating miRNA-195 as a diagnostic biomarker for the early detection of cervical cancer [
24]. Cai et al. showed the association between decreased serum miRNA-195 expression and positive distant metastasis, advanced clinical stage, and poor overall survival and disease-free survival in human osteosarcoma [
25]. In addition, serum miRNA-195 was predictive of recurrence risk in adrenocortical cancer patients [
22]. In patients with breast cancer, serum miRNA-195 had a higher sensitivity for detecting tumor response to neoadjuvant chemotherapy than conventional tumor markers such as CEA and CA153. The potential diagnostic and prognostic value of blood miRNA-195 in other human malignancies would be an interesting and important topic of future investigations.
Recently, Zhao et al. showed upregulation of miRNA-195 expression in tumor tissues and plasma of NSCLC patients and reported that there was no significant association between plasma miRNA-195 level and patient survival [
33]. These results are surprising because decreased miRNA-195 expression has been reported in many human cancers including NSCLC. Zhou et al. demonstrated miRNA-195 downregulation in NSCLC samples and cell lines [
34]. Liu et al. confirmed decreased miRNA-195 expression in NSCLC tumor tissues and its association with poor survival [
26]. In vitro and in vivo functional assays revealed that miRNA-195 overexpression suppressed NSCLC growth, migration, and invasion [
26,
34]. We suggest further studies with larger sample size to clarify miRNA-195 expression and its clinical and prognostic significance in NSCLC.
It is now clear that miRNAs exhibit oncogenic or tumor suppressive properties by regulation of target gene expression. MicroRNA-195 inhibits proliferation, invasion, and metastasis in breast cancer cells by targeting FASN, HMGCR, ACACA, and CYP27B1 [
35]. MicroRNA-195 suppresses glucose uptake and proliferation of human bladder cancer cells by regulating GLUT3 expression [
36]. MicroRNA-195 promotes apoptosis and suppresses tumorigenicity of human colorectal cancer cells by downregulating Bcl-2 [
37]. In NSCLC, MYB and CHEK1 have been confirmed as direct targets of miRNA-195 [
26,
34]. Previous studies have confirmed that there is no “one-to-one” connection between miRNAs and target mRNAs. An average miRNA can have more than 100 targets [
38]. Conversely, several miRNAs can converge on a single transcript target. Thus, the potential regulatory circuitry afforded by miRNA-195 may be enormous, and the accurate molecular mechanisms on how miRNA-195 mediates NSCLC carcinogenesis and development need further clarification.
Conclusions
In summary, the current study showed that the level of plasma miRNA-195 was downregulated in NSCLC patients and associated with aggressive clinicopathological characteristics. More importantly, decreased plasma miRNA-195 could distinguish NSCLC from healthy control and predict poor patient survival. Based on these results, plasma miRNA-195 might serve as a reliable minimally invasive biomarker for early detection and prognostic evaluation of NSCLC.