【摘 要】
:
AIM: To clarify the influence of genetic polymorphisms on colorectal cancer.METHODS: The results of 42 related studies from 1990 to 2001 were analyzed by meta-a
【机 构】
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Department of Epidemiology and Health Statistics
【基金项目】
:
the National Natural Science Foundation of China
论文部分内容阅读
AIM: To clarify the influence of genetic polymorphisms on colorectal cancer.METHODS: The results of 42 related studies from 1990 to 2001 were analyzed by meta-analysis. Mantel-Haenzel fixed-effect model or Dersimonian-Laird random-effect model and ReviewManager 4.1 statistical program were applied in processing the data.RESULTS: Meta analysis of these studies showed that GSTT1 deletion (pooled OR = 1.42), N-acetyltransferase 2 (NAT2)-rapid acetylator phenotype and genotye (pooled OR = 1.08)and NAT2-rapid acetylator phenotype (pooled OR = 1.15)had a significantly increased risk for colorectal cancer (P<0.05), other genotypes like GSTM1 deletion, GSTP1 1le105Val, NAT1*10, NAT2-rapid acetylator genotype CYP1A1 L1e462Val, CYP1A1 MspI*C, MTHFR C677T and MTR A2759G had no significant relationship with colorectal cancer (P>0.05).CONCLUSION: Risks for colorectal cancer are significantly associated with the genetic polymorphisms of GSTT1 deletion,NAT2-rapid acetylator phenotype and genotye and NAT2-rapid acetylator phenotype.
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