Literature DB >> 16969494

Breast cancer risk and polymorphisms in genes involved in metabolism of estrogens (CYP17, HSD17beta1, COMT and MnSOD): possible protective role of MnSOD gene polymorphism Val/Ala and Ala/Ala in women that never breast fed.

Susana N Silva1, Marisa N Cabral, Guilherme Bezerra de Castro, Marcelo Pires, Ana Paula Azevedo, Isabel Manita, Julieta Esperança Pina, José Rueff, Jorge Gaspar.   

Abstract

Polymorphisms in genes encoding enzymes involved in estrogen metabolism are held to be candidates for associations with breast disease, since there is evidence that circulating estrogens are associated with breast cancer risk. In this study, we evaluated the frequency of different polymorphisms related with estrogen metabolism [COMT Val158Met, CYP17 (5'UTR, T27C); HSD17beta1 Gly313Ser and MnSOD Val16Ala] in a breast cancer resistant population, the Xavante Indians, and the frequencies were compared with the ones reported in other populations where breast cancer case-control studies dealing with these polymorphisms have been carried out. The data obtained showed that, apart from the MnSOD Val16Ala polymorphism where the frequency of the variant allele was much higher than that reported in other populations, all the others were within the range reported in other populations. Considering these data we carried out a case-control study in the Portuguese population (241 cases and 457 controls) in order to evaluate the potential role of this polymorphism in breast cancer susceptibility. The results obtained did not reveal a significant association between individual genotypes and breast cancer risk. However, when the population was stratified for breast feeding, it was observed that for the patients that never breast fed the presence of the variant allele (Ala) was marginally associated with a decreased risk for this pathology (adjusted OR: 0.575 (0.327-1.011). These data seem to suggest that individuals who never breast fed with MnSOD Val16Ala variant allele are at a lower risk for breast cancer, but larger studies are required to confirm these results.

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Year:  2006        PMID: 16969494

Source DB:  PubMed          Journal:  Oncol Rep        ISSN: 1021-335X            Impact factor:   3.906


  7 in total

1.  There is no relationship between SOD2 Val-16Ala polymorphism and breast cancer risk or survival.

Authors:  Chengdi Wang; Yang Liu; Jian Zhou; Lei Ye; Nan Chen; Min Zhu; Yulin Ji
Journal:  Mol Clin Oncol       Date:  2017-08-14

2.  Plasma selenium, manganese superoxide dismutase, and intermediate- or high-risk prostate cancer.

Authors:  June M Chan; William K Oh; Wanling Xie; Meredith M Regan; Meir J Stampfer; Irena B King; Miyako Abe; Philip W Kantoff
Journal:  J Clin Oncol       Date:  2009-06-15       Impact factor: 44.544

3.  Polymorphisms in HSD17B1: Early Onset and Increased Risk of Alzheimer's Disease in Women with Down Syndrome.

Authors:  Joseph H Lee; Susan Gurney; Deborah Pang; Alexis Temkin; Naeun Park; Sarah C Janicki; Warren B Zigman; Wayne Silverman; Benjamin Tycko; Nicole Schupf
Journal:  Curr Gerontol Geriatr Res       Date:  2012-03-04

4.  Male and female breast cancer: the two faces of the same genetic susceptibility coin.

Authors:  Susana Nunes Silva; Bruno Costa Gomes; Saudade André; Ana Félix; António Sebastião Rodrigues; José Rueff
Journal:  Breast Cancer Res Treat       Date:  2021-05-03       Impact factor: 4.872

Review 5.  Association of COMT Val158Met polymorphism and breast cancer risk: an updated meta-analysis.

Authors:  Xue Qin; Qiliu Peng; Aiping Qin; Zhiping Chen; Liwen Lin; Yan Deng; Li Xie; Juanjuan Xu; Haiwei Li; Taijie Li; Shan Li; Jinmin Zhao
Journal:  Diagn Pathol       Date:  2012-10-08       Impact factor: 2.644

Review 6.  Modulation of MnSOD in Cancer:Epidemiological and Experimental Evidence.

Authors:  Aekyong Kim
Journal:  Toxicol Res       Date:  2010-06

7.  Association between MnSOD Val16Ala Polymorphism and Cancer Risk: Evidence from 33,098 Cases and 37,831 Controls.

Authors:  Ping Wang; Yanfeng Zhu; Shoumin Xi; Sanqiang Li; Yanle Zhang
Journal:  Dis Markers       Date:  2018-09-02       Impact factor: 3.434

  7 in total

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