Abstract | BACKGROUND: OBJECTIVES: An updated meta-analysis was performed to solve the controversy. METHODS: Meta-analyses of Observational Studies in Epidemiology (MOOSE) guidelines were used. RESULTS: Overall, the GSTM1 null genotype was associated with an increased CRC risk in Caucasians (odds ratio (OR) = 1.14, 95% confidence interval (CI): 1.05-1.23), Asians (OR = 1.19, 95% CI: 1.08-1.32), high-quality studies (OR = 1.12, 95% CI: 1.06-1.18). Moreover, the GSTM1 null genotype was also associated with an increased colon cancer risk (OR = 1.32, 95% CI: 1.16-1.51). The GSTT1 null genotype was also associated with an increased CRC risk in Asians (OR = 1.08, 95% CI: 1.02-1.15) and Caucasians (OR = 1.24, 95% CI: 1.09-1.41). Moreover, The GSTT1 null genotype was associated with an increased rectal cancer risk (OR = 1.13, 95% CI: 1.01-1.27, I2 = 8.3%) in subgroup analysis by tumor location. Last, the GSTM1 null/GSTT1 null genotype was associated with an increased CRC risk in Asians. CONCLUSION: This meta-analysis indicates that the GSTM1 and GSTT1 null genotypes are associated with increased CRC risk in Asians and Caucasians, and the GSTM1 null/GSTT1 null genotype was associated with increased CRC risk in Asians.
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Authors | Liang Song, Chen Yang, Xiao-Feng He |
Journal | Bioscience reports
(Biosci Rep)
Vol. 40
Issue 8
(08 28 2020)
ISSN: 1573-4935 [Electronic] England |
PMID | 32776111
(Publication Type: Journal Article, Meta-Analysis)
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Copyright | © 2020 The Author(s). |
Chemical References |
- Biomarkers, Tumor
- glutathione S-transferase M1
- glutathione S-transferase T1
- Glutathione Transferase
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Topics |
- Humans
- Asian People
(genetics)
- Biomarkers, Tumor
(genetics)
- Case-Control Studies
- Colorectal Neoplasms
(diagnosis, ethnology, genetics)
- Genetic Association Studies
- Genetic Predisposition to Disease
- Glutathione Transferase
(genetics)
- Observational Studies as Topic
- Polymorphism, Genetic
- Risk Assessment
- Risk Factors
- White People
(genetics)
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