SMAD7 polymorphisms and colorectal cancer risk: a meta-analysis of case-control studies
Autor: | Wenting Wu, Yongsheng Huang, Meng Nie, Chuang Li, Lin Wang |
---|---|
Rok vydání: | 2016 |
Předmět: |
Risk
0301 basic medicine Oncology Gerontology medicine.medical_specialty Genotype Colorectal cancer colorectal cancer Subgroup analysis Polymorphism Single Nucleotide Smad7 Protein polymorphism 03 medical and health sciences SMAD7 0302 clinical medicine Mothers against decapentaplegic homolog 7 Internal medicine Epidemiology Odds Ratio medicine Humans Genetic Predisposition to Disease Alleles Genetic Association Studies business.industry Case-control study Odds ratio medicine.disease Confidence interval meta-analysis 030104 developmental biology Case-Control Studies 030220 oncology & carcinogenesis Meta-analysis Colorectal Neoplasms business Publication Bias Research Paper |
Zdroj: | Oncotarget |
ISSN: | 1949-2553 1295-3717 |
Popis: | // Yongsheng Huang 1 , Wenting Wu 2 , Meng Nie 1 , Chuang Li 1 , Lin Wang 1 1 Institute of Basic Medical Sciences and School of Basic Medicine, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China 2 Department of Epidemiology, Richard M. Fairbanks School of Public Health, Melvin & Bren Simon Cancer Center, Indiana University, Indianapolis, IN 46202, USA Correspondence to: Yongsheng Huang, email: yongsheng@ibms.pumc.edu.cn Lin Wang, email: lin.wang@ibms.pumc.edu.cn Keywords: SMAD7, colorectal cancer, polymorphism, meta-analysis Received: April 15, 2016 Accepted: September 14, 2016 Published: September 27, 2016 ABSTRACT Mothers against decapentaplegic homolog 7 ( SMAD7 ) inhibits the transforming growth factor-β (TGF-β) signaling pathway, which regulates carcinogenesis and cancer progression. A number of studies have reported that SMAD7 polymorphisms (rs4464148, rs4939827, and rs12953717) are associated with colorectal cancer (CRC) risk, but the results from these studies remain conflicting. To determine a more precise estimation of the relationship between SMAD7 and CRC, we undertook a large-scale meta-analysis of 63 studies, which included a total of 187,181 subjects (86,585 cases and 100,596 controls). The results of our meta-analysis revealed that the C allele of rs4464148 [CC vs. TT+TC, odds ratio (OR) =1.23, 95% confidence interval (CI): 1.14–1.33, P < 0.01], the T allele of rs4939827 [TT vs. CC+TC, odds ratio OR=1.15, 95%CI:1.07–1.22, P < 0.01] and the T allele of rs12953717 [TT vs. CC+TC, OR =1.22, 95%CI:1.16–1.29, P < 0.01] were all associated with the increased CRC risk. Subgroup analysis according to ethnicity showed rs4464148 and rs12953717 were associated with the risk of CRC in both Caucasians and Asians, whereas rs4939827 was a risk polymorphism for CRC specifically in Caucasians. In summary, this large-scale meta-analysis indicated that SMAD7 polymorphisms (rs4464148, rs4939827, and rs12953717) correlate with CRC. |
Databáze: | OpenAIRE |
Externí odkaz: |