Literature DB >> 21479914

Variation in the CYP19A1 gene and risk of colon and rectal cancer.

Martha L Slattery1, Abbie Lundgreen, Jennifer S Herrick, Susan Kadlubar, Bette J Caan, John D Potter, Roger K Wolff.   

Abstract

CYP19A1, or aromatase, influences estrogen-metabolizing enzymes and may influence cancer risk. We examine variation in the CYP19A1 gene and risk of colorectal cancer using data from population-based case-control studies (colon n = 1,574 cases, 1,970 controls; rectal n = 791 cases, 999 controls). Four SNPs were statistically significantly associated with colon cancer and four were associated with rectal cancer. After adjustment for multiple comparisons, the AA genotype of rs12591359 was associated with an increased risk of colon cancer (OR 1.44 95% CI 1.16-1.80) and the AA genotype of rs2470144 was associated with a reduced risk of rectal cancer (OR 0.65 95% CI 0.50-0.84). Variants of CYP19A1 were associated with CIMP+ and CIMP+/KRAS2-mutated tumors. CT/TT genotypes of rs1961177 were significantly associated with an increased likelihood of a MSI+ colon tumor (OR 1.77 95% CI 1.26-2.37). We observed statistically significant interactions between genetic variation in NFκB1 and CYP19A1 for both colon and rectal cancer. Our data suggest the importance of CYP19A1 in the development of colon and rectal cancer and that estrogen may influence risk through an inflammation-related mechanism.

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Year:  2011        PMID: 21479914      PMCID: PMC3225228          DOI: 10.1007/s10552-011-9768-x

Source DB:  PubMed          Journal:  Cancer Causes Control        ISSN: 0957-5243            Impact factor:   2.506


  45 in total

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7.  Potentially functional SNPs (pfSNPs) as novel genomic predictors of 5-FU response in metastatic colorectal cancer patients.

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8.  CYP19A1 gene polymorphism and colorectal cancer etiology in Saudi population: case-control study.

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9.  Lamellipodin-Deficient Mice: A Model of Rectal Carcinoma.

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Journal:  Br J Cancer       Date:  2016-01-14       Impact factor: 7.640

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