Abstract

Background. The associations between polymorphisms in microRNAs and the susceptibility of colorectal cancer (CRC) were inconsistent in previous studies. This study aims to quantify the strength of the correlation between the four common polymorphisms among microRNAs (hsa-mir-146a rs2910164, hsa-mir-149 rs2292832, hsa-mir-196a2 rs11614913, and hsa-mir-499 rs3746444) and CRC risk. Methods. We searched PubMed, Web of Knowledge, and CNKI to find relevant studies. The combined odds ratio (OR) with 95% confidence interval (95% CI) was used to estimate the strength of the association in a fixed or random effect model. Results. 15 studies involving 5,486 CRC patients and 7,184 controls were included. Meta-analyses showed that rs3746444 had association with CRC risk in Caucasians (OR = 0.57, 95% CI = 0.34–0.95). In the subgroup analysis, we found significant associations between rs2910164 and CRC in hospital based studies (OR = 1.24, 95% CI = 1.03–1.49). rs2292832 may be a high risk factor of CRC in population based studied (OR = 1.18, 95% CI = 1.08–1.38). Conclusion. This meta-analysis showed that rs2910164 and rs2292832 may increase the risk of CRC. However, rs11614913 polymorphism may reduce the risk of CRC. rs3746444 may have a decreased risk to CRC in Caucasians.

Highlights

  • Colorectal cancer (CRC) is the third leading cause of cancer death for both men and women in the USA [1]

  • Relevant articles were independently searched by two authors (Wang M and Dai ZJ) in PubMed, Web of Science, and Chinese National Knowledge Infrastructure (CNKI)

  • HWE, the results showed a significant association between rs11614913 polymorphism and colorectal cancer (CRC) risk in the homozygous genetic model (TT versus CC: odds ratio (OR) = 0.80, 95% confidence interval (95% confidence interval (CI)) = 0.68–0.95, P = 0.009)

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Summary

Introduction

Colorectal cancer (CRC) is the third leading cause of cancer death for both men and women in the USA [1]. The associations between polymorphisms in microRNAs and the susceptibility of colorectal cancer (CRC) were inconsistent in previous studies. Meta-analyses showed that rs3746444 had association with CRC risk in Caucasians (OR = 0.57, 95% CI = 0.34–0.95). We found significant associations between rs2910164 and CRC in hospital based studies (OR = 1.24, 95% CI = 1.03–1.49). Rs2292832 may be a high risk factor of CRC in population based studied (OR = 1.18, 95% CI = 1.08–1.38). This meta-analysis showed that rs2910164 and rs2292832 may increase the risk of CRC. Rs11614913 polymorphism may reduce the risk of CRC. Rs11614913 polymorphism may reduce the risk of CRC. rs3746444 may have a decreased risk to CRC in Caucasians

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