作者: Dongfeng He , Lihong Ma , Rennan Feng , Liangcai Zhang , Yongshuai Jiang
DOI: 10.1016/J.BIOPHA.2015.08.023
关键词:
摘要: Colorectal cancer (CRC) is the third most common form of and second leading cause cancer-related death in Western countries. In order to detect CRC genetic variants, genome-wide association studies (GWAS) have been performed reported some novel susceptibility variants. RHPN2 located on 9q13.11, which encodes a member rhophilin family Ras-homologous (Rho)-GTPase binding proteins. gene rs10411210 polymorphism was identified be significantly associated with European ancestry. GWAS candidate investigate whether risk European, Asian American populations. However, no association. Evidence shows that variant may prognostic biomarker for patients surgically resected CRC. Here we reevaluated this using large-scale samples from 15 (131580 including 53564 cases 78016 controls) meta-analysis method by searching PubMed Google Scholar databases. We did not identify significant heterogeneity among these (P=0.4201 I(2)=2.8%). Our results showed between (P=9.17E-14, odds ratio (OR)=1.10, 95% confidence interval (CI) 1.07-1.13). subgroup analysis, found population P=5.70E-09, OR=1.14, CI 1.10-1.20 P=3.36E-07, OR=1.11, 1.07-1.16, but P=0.0576, OR=1.05, 1.00-1.09. Collectively, our analysis further highlights colorectal cancer.