J Cancer 2018; 9(18):3334-3342. doi:10.7150/jca.25514 This issue

Research Paper

Prognostic Role of MicroRNA-497 In Cancer Patients: A Meta-analysis

Jiaxi Feng1#, Xi Gu1#, Liyang Liu1#, Ming Lu1, Xiang Ma1, Yang Cao1, Rongjiang Jiang2, Baolin Wang1, Qinghong Zhao1 Corresponding address

1. Department of General Surgery, the Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
2. Department of Urology, the Second Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China
# Equal contributors and co-first authors.

This is an open access article distributed under the terms of the Creative Commons Attribution (CC BY-NC) license (https://creativecommons.org/licenses/by-nc/4.0/). See http://ivyspring.com/terms for full terms and conditions.
Feng J, Gu X, Liu L, Lu M, Ma X, Cao Y, Jiang R, Wang B, Zhao Q. Prognostic Role of MicroRNA-497 In Cancer Patients: A Meta-analysis. J Cancer 2018; 9(18):3334-3342. doi:10.7150/jca.25514. Available from https://www.jcancer.org/v09p3334.htm

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Background: MicroRNA-497(miR-497) has been studied for its irreplaceable role of predicting the prognosis of various cancers, but there has been no systematic study to summarize the data. Consequently, we performed this meta-analysis to reveal the association between the expression level of miR-497 and cancer prognosis systematically.

Materials and Methods: PubMed was searched for appropriate studies and a total of 12 eligible publications with 989 cancer patients were recruited into our analysis to assess the strength of the association. Hazard ratios (HRs) and odds ratios (ORs) were analyzed to finish this work.

Results: The cancer patients who have high expressing level of miR-497 are less possible to have lymph node metastasis (OR = 0.25, 95% CI: 0.16-0.40, P < 0.001) and more likely to have favourable tumor-node-metastasis stage (OR = 0.29, 95% CI: 0.17-0.49, P < 0.001). Also, high miR-497 expression level was notably connected to better overall survival (pooled HR = 0.41, 95% CI: 0.32-0.53, P < 0.001).

Conclusions: High expressing levels of miR-497 might be a potential biomarker which can be used to predict the better prognosis of different cancer types.

Keywords: prognosis, biomarker, microRNA-497, cancer, meta-analysis


Although the amount of deaths owing to cancers continued to decline in recent years, in both developing and developed countries, the main cause of death is cancer especially in less developed regions which have the 82% of the world's population [1,2]. In China, it is estimated that a total of 4292000 new cases of cancer and 2814000 deaths due to cancers had occurred in 2015[3]. Although the previous diagnostic and treatment modalities have been greatly improved in recent years, the 5-year survival rate for patients with different cancer types still remains low [4]. Patients will get better survival chances and higher quality of life, if cancers can be observed early and effective treatment can be given promptly. But when the patients are diagnosed with advanced cancer stage, the effectiveness of the treatment is limited. Therefore, there is urgent necessity for a new biomarker to predict tumor metastasis and prognosis.

A family of endogenous small non-coding RNAs has been named as MicroRNAs (miRNAs), whose target mRNAs expression have been suppressed by blinding to the 3'-UTR on the basis of both complementary sequence and potential target site. MiRNAs will inhibit target mRNAs translation or degradation to negatively regulate gene expression [5,6]. There is a massive amount of evidence showed that many biological procedures for example cell proliferation, cell cycle, apoptosis, migration, invasion, and differentiation can be regulated by miRNAs [6,7]. In addition, the emerging evidence suggested that miRNAs may play an important role in carcinogenesis or tumor suppression in humans [8,9].

It shows that the first intron of the MIR497HG (Gene ID: 10050675) gene on human chromosome 17p13.1 has encoded the MicroRNA-497 (miR-497) which is a highly conserved miRNA [10]. MiR-497 was first reported in human breast cancer [11]. Loss of miR-497 expression has been reported in many cancer types, whereas restoration of miR-497 expression has been shown to abrogate tumorigenesis [12-14]. Also, several targets of miR-497 have been identified previously, for example, CCND1, CCNE1, Bcl-w and BDNF [15-18]. Plenty of studies have discovered the down-regulation of miR-497 in various types of cancers, containing ovarian cancer [19,20], gastric cancer [21,22], clear cell renal cell carcinoma [23], diffuse large B-cell lymphoma [24], non-small cell lung cancer [25], hepatocellular carcinoma [26], osteosarcoma [27,28], gliomas[29], thyroid cancer [30], renal cell carcinoma [31]. Until now, numerous studies have demonstrated that clinicopathological features and the patients' overall survival time in various types of cancers are closely associated with the dysregulation of miR-497. However, most individual studies have their limits, for example, the sample size is small or obtaining controversial results, and so on. To further reveal the association between the miR-497 expression level and the clinical prognosis of cancer patients, we performed this meta-analysis.

Materials and Methods

Periodical search

We retrieved the PubMed database for reports published in English up to 31 January 2018. The following key words were used for the research: “microRNA-497” or “miR-497” and “cancer” or “carcinoma”. Primary publication in reference was also considered to acquire excess concerned articles.

Inclusion and exclusion criteria

If the study met the next criteria, would be included in this article: (1) the published articles were in English; (2) analyzing the prognostic role of miR-497 in cancer patients; (3) grouping the patients according to the expressing level of miR-497; (4) containing the association between clinicopathological parameters and miR-497 expression level; (5) providing adequate statistics to conjecture HRs with a corresponding 95% CI for OS. Research, reviews and case reports that did not provide enough data will not be contained in this meta-analysis. If the similar content is available more than once, only the most recent publications are contained.

Data extraction and quality valuation

Each study was revised by two authors, and they extracted enough valuable data based on the above criteria. The information below was gathered from the contained studies: the cognomen of first author; publication year; cancer types; nation; detecting miR-497 methods; over-all number of patients; quantity of LNM patients; the number of patients with different TNM stage in high and low miR-497 expression level groups; cut-off value; the follow-up time; HRs and the corresponding 95% CI for OS. Multivariate analysis effects are preferred, when the article provided both univariate and multivariate analysis. Any divergence was solved by reaching a consensus with other authors. To assess the quality of the pooled study, we performed the Newcastle-Ottawa Scale (NOS). High quality required an NOS score ≥6.

Statistical methods

The association between the expressing level of miR-497 and clinical prognosis was assessed by using ORs or HRs with 95% CIs. The heterogeneity contained in the pooled studies was evaluated by I2 based Q test and I2 index. We prioritized the use of fixed-effects models, if the Q test showed no significant heterogeneity in qualitative studies, defined as P heterogeneity > 0.05 and / or I2 < 50% [32]. Else, we used a random-effects model [33]. We conducted sensitivity analysis to assess the contribution of the individual study to the pooled HR, so that, we could estimate the stability of our results. The Kaplan-Meier curve provided the HRs and 95% CIs for OS with the help of the Engauge Digitizer 4.1 software [34]. We evaluate the publication bias through the Begg's funnel plot, and P < 0.05 means obvious publication bias [35]. Stata software was used to complete the statistical analyses (version 13.0, Stata Corp, College Station, USA).


Features of studying

As shown in Figure 1, 134 publications were acquired from PubMed databases. 120 publications were excluded because of the lack of necessary data that we need and 14 publications were selected for further full-text review after we reviewed the abstracts and the full texts. One of the left 14 publications was retracted by the press, so it was excluded. In the left 13 publications, two publications were written by the same author and shared the same clinical data, so we chose the one which was the most recent and had more detailed data that we needed. At last, 12 studies were enrolled. Among these studies, the cancer types were ovarian cancer [19], gastric cancer [21,22], clear cell renal cell carcinoma [23], diffuse large B-cell lymphoma [24], non-small cell lung cancer [25], hepatocellular carcinoma [26], osteosarcoma [27,28], gliomas [29], thyroid cancer [30], renal cell carcinoma [31]. In table 1, the features of the involved studies were indicated.

 Figure 1 

Flowchart of included publications.

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 Table 1 

Characteristics of studies included in this meta-analysis

StudyCountryYearCancer typeMicroRNA-497 expressionMicroRNA-497 assayHR statisticHR (95%CI) high/lowSurvival analysisNOSCut-off valueFollow-up (months)
Wang [19]China2014OC381727584038qRT-PCRSurvival curve0.92 (0.42-2.01)Univariate8-60
Li [21]China2014GC482224493630qRT-PCRSurvival curve0.37 (0.20-0.68)Univariate8Median value60
Zhao [23]China2015ccRCC3828481126qRT-PCRDate in paper0.39 (0.16-0.59)Multivariate8Mean level60
Katharina [24]Austria2015DLBCL29-1629-17qRT-PCRDate in paper0.36 (0.12-1.01)Univariate7Median value120
Huang [25]China2015NSCLC257-2613-qRT-PCRSurvival curve0.44 (0.22-0.91)Univariate7Median value60
Zhang [26]China2016HCC43-443-15qRT-PCRDate in paper0.47 (0.28-0.81)Multivariate7Median value60
Pang [27]China2016OS94-2091-54qRT-PCRDate in paper0.26 (0.12-0.50)Multivariate7Median value70
Feng [29]China2016Gliomas52-1658-48qRT-PCRDate in paper0.30 (0.14-0.91)Multivariate7Median value60
Song [28]China2017OS19-327-16qRT-PCR---6Mean level72
Liu [22]China2017GC38-1748-34qRT-PCR---6Mean level-
Wang [30]China2017TC2112271415qRT-PCR---7Mean level-
Sun [31]China2017RCC1412261210qRT-PCR---7--

Note: The dashes mean no data.

III/IV: TNM stage III/IV; LNM: lymph node metastasis; OC: ovarian cancer; GC: gastric cancer; ccRCC: clear cell renal cell carcinoma; DLBL: diffuse large B-Cell lymphoma; NSCLC: non-small cell lung cancer; HCC: hepatocellular carcinoma; OS: osteosarcoma; TC: thyroid cancer; RCC: renal cell carcinoma

 Figure 2 

Forest plot for the association between expressing levels of miR-497 and TNM stage: subgroup analysis by cancer type.

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Association between expression level of miR-497 and TNM stage (III/IV vs. I/II)

Figure 2 has showed that a random-effects model was used to analyze the pooled odds ratio (OR) and its 95% CI, as the result of the obvious heterogeneity among these eleven reports (I2 = 67.7%, P = 0.001). Consequently, we detected that the high expressing level of microRNA-497 (miR-497) was predictive of favorable tumour-node-metastasis (TNM) stage (OR = 0.29, 95% CI: 0.17-0.49, P < 0.001). Because of the discovery of the heterogeneity, we performed the subgroup analysis of the data by cancer types and sample size. The results showed that the high miR-497 expressing level was related with lower TNM stage in gastric cancer (OR = 0.47, 95% CI: 0.25-0.89, P = 0.02), osteosarcoma (OR = 0.17, 95% CI: 0.10-0.31, P < 0.001), but not existed in ovarian cancer (OR = 1.29, 95% CI: 0.53-3.13, P = 0.57). At the same time, we performed another subgroup analysis by sample sizes. The sample size of the contained studies ranged from 40 to 185. We find a significant association between TNM stage and the miR-497 expression level in a subgroup with simple sizes > 100 (OR = 0.14, 95% CI: 0.07-0.27, P < 0.001) (Figure 3). During our work, if the 50 and 90 were chosen as the classification criteria for the sample size, we found an obvious heterogeneity in the smaller sample size group (data not shown).

Association between miR-497 expression level and lymph node metastasis

A total of 6 studies with 418 cancer patients were involved in this lymph node metastasis (LNM) analysis. We chose a fixed-effect model to complete the comparison between high miR-497 expression level and low miR-497 expression level (I2 = 0.0%, P = 0.434). The results showed that patients with low miR-497 expression level were more likely to have lymph node metastases (OR = 0.25, 95% CI: 0.16-0.40, P < 0.001) (Figure 4).

Association between expression level of miR-497 and overall survival

Eight studies with 769 patients were included to gain a pooled HR and 95% CI for overall survival (OS) in various types of cancer. In this analysis, a fixed-effects model had been adopted because no heterogeneity was discovered in the OS group (I2 = 0.0%, P = 0.476). Through this analysis, we discovered a significant association between high expression level of miR-497 and better overall survival (pooled HR = 0.41, 95% CI: 0.32-0.53, P < 0.001) (Figure 5).

 Figure 3 

Forest plot for the association between expressing levels of miR-497 and TNM stage: subgroup analysis by sample size.

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 Figure 4 

Forest plot for the association between miR-497 and LNM.

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Sensitivity analysis and publication bias

To assess the steadiness and reliability of our meta-analysis, we analyzed the sensitivity of the OS group through the way that we omitted each study from our analysis one at a time. The results showed no individual study affected the pooled HR (Figure 6). Furthermore, analysis of sensitivity indicated that there were no significant effects on the association between the pooled OR for elevated miR-497 and TNM stage or LNM when we excluded any of the studies (data not shown). Publication bias for the meta-analysis was assessed by Begg's funnel plot analysis (P = 0.711) and Egger's linear regression test was used to verify the accuracy of the Begg's funnel plot (P = 0.804). No significant publication bias was found through the two tests (Figure 7).


As one of small regulatory RNA molecules, miRNA can moderate the expression of their target genes. MiRNAs can blind to the 3'UTR and 5'UTR of their target mRNAs so that they can mediate degradation or translational repression of the mRNAs [36]. Studies have demonstrated that miRNAs have broad effects on numerous biological processes, including differentiation, metastasis, apoptosis, metabolism and maturation [37,38]. The importance of miRNAs expression levels in various cancers and their potential utility as prognostic factors have become apparent. Plenty of evidence has suggested that miRNAs can regulate tumor proliferation and invasion, and they are widely analyzed in diagnosis, therapies and prognosis of various cancers [39,40]. A quantity of miRNAs have been discovered to be associated with the clinical characteristics of various cancers, due to the obvious impact of miRNAs on gene expression. These miRNAs include miR-218[41], miR-21 [42], and miR-539 [43]. This means that miRNAs have the potential value to become the tumor biomarker, forecasting prognosis, therapeutic efficacy.

 Figure 5 

Forest plot of pooled HRs of high expression level of miR-497 for OS.

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 Figure 6 

Consequence of sensitivity analysis

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 Figure 7 

Funnel plot analysis of potential publication bias (Begg's test).

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MiR-497 has been studied for many years, but it is still a popular studying topic currently. Previous studies have suggested that miR-497 was a tumor-associated miRNA in various cancers such as oral colorectal cancer, non-small cell lung cancer and squamous cell carcinoma et al [44-46]. The mechanism by which miR-497 promotes tumor progression has been complicated, also, more studies are needed to reveal this. Liu et al. [47] found that miR-497 might promote tumor progression in breast cancer, which could target SMAD family number 7 (SMAD7) mRNA to inhibit the breast cancer cell growth and invasion. Xu et al.[48] found that miR-497 served a significant role in suppressing colorectal cancer (CRC) cell growth via inhibition of insulin receptor substrate 1 (IRS1). Yu et al.[49] discovered that miR-497 was down-regulated in samples of multiple myeloma (MM) and cell lines, also, it could directly target pre-B-cellleukemia transcription factor 3 (PBX3) to promote the malignant progression in MM. Zhang et al.[50] found that miR-497 suppresses the proliferation and invasion of the bladder transitional cell carcinoma (BTCC) cells, possibly through modulating the target gene E2F transcription factor 3 (E2F3).

Recently, a variety of reports have suggested the association between the expressing level of miR-497 and the various cancers prognosis. To verify the potential predictive value of miR-497 expression level, we conducted this meta-analysis of 12 studies including 989 cancer patients. We noticed that the lower expressing level of miR-497 significantly means unfavorable LNM and TNM stage for cancer patients. Through merging HRs from included studies, we noticed that the higher expressing level of miR-497 was associated with the longer overall survival time. Also, patients with higher level expressing of miR-497 had longer OS time compared with those with lower expressing levels. Yet, our meta-analysis is not impeccable because of the limitation of the data in the included publications. Because of the lack of some necessary data, we were not allowed to perform the meta-analysis to assess the association between the miR-497 expression level and survival without disease, survival without progression, survival without event. Obvious heterogeneity was discovered when we conducted the TNM stage group analysis. In order to find out the origin of heterogeneity, we performed an analysis in subgroups by cancer types and size of sample. No obvious heterogeneity was found in the subgroup with sample size > 100, and when we left the Wang [19] study out of the subgroup with size of sample < 100. There is also no observation of significant heterogeneity. So we reflected that the main source of heterogeneity was the variance in size of sample and the Wang [19] study. In his study, the sample size of patients with low expression is much larger than the ones with high expression. Also, we considered that Wang [19] study has more distinct individual variation than the other included studies. However, we could not be very sure the origin of the heterogeneity because the entire sample size of the involved studies is small. In a word, through our meta-analysis, we found that miR-497 might be vital in tumor progression and could be very valuable to work as a new biomarker to predict clinical outcomes in patients with cancer.

As far as we know, our work is the first study to use meta-analysis to assess the clinical value of the expressing level of miR-497 in cancer patients. Nonetheless, our study also had the limitation that cannot be ignored. Firstly, only 12 studies with 989 patients were pooled in our analysis, so it is less reliable to some extent. Secondly, because of the limited publications, we ignored the subgroup analysis according to age, sex, and so on, but cancer progression is associated with many factors. Thirdly, direct access to some HRs in the study cannot be achieved, so we had to estimate and extract HRs through the survival curves or calculate HRs through the reported data. This reduced the credibility of our results. Last but not least, the cut-off value distinguishing high or low levels of miR-497 differed from these studies. To solve this, more studies and larger sample sizes were needed.

In summary, as shown in the results of our meta-analysis that high miR-497 expression level in different cancer types is significantly associated with favourable TNM stage, no LNM, and longer OS time. Therefore, miR-497 may become a new and valuable biomarker for predicting well prognosis in cancer patients. We hope that this result can be paid enough attention to, so that, more cancer patients can benefit from our scientific research.

Competing Interests

The authors have declared that no competing interest exists.


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Author contact

Corresponding address Corresponding author: Qinghong Zhao, Department of General Surgery, The Second Affiliated Hospital of Nanjing Medical University, 121 Jiangjia Yuan Road, Nanjing 210011, Jiangsu, China. E-mail: njzhqhcom

Received 2018-2-12
Accepted 2018-7-16
Published 2018-9-7