Literature DB >> 28427168

Association between BRCA1 P871L polymorphism and cancer risk: evidence from a meta-analysis.

Limin Miao1, Yang Yu1, Yefeng Ji1, Bo Zhang1, Zhiyao Yuan1, Yifei Du1, Longbiao Zhu1, Ruixia Wang1, Ning Chen1,2, Hua Yuan1,2.   

Abstract

Breast cancer 1 (BRCA1) gene makes great contributions to the repair of DNA. The association between BRCA1 P871L polymorphism and cancer risk has been investigated in a growing number of studies, but the conclusions are not conclusive. To obtain a comprehensive conclusion, we performed a meta-analysis of 24 studies with 13762 cases and 22388 controls. The pooled results indicated that BRCA1 gene P871L variant decreased risk of overall cancer (homozygous model: odds ratio (OR) = 0.89, 95%confidence interval (CI) = 0.79-1.00; recessive model: OR = 0.89, 95% CI = 0.80-0.99). The stratified analysis observed decreased risk associated with BRCA1 P871L in subgroups among Asians and high score studies, but not Caucasians or low score studies. In conclusion, despite several limitations, this meta-analysis suggested that BRCA1 P871L genetic variation may be associated with decreased susceptibility to cancer.

Entities:  

Keywords:  BRCA1; cancer risk; meta-analysis; polymorphism

Mesh:

Year:  2017        PMID: 28427168      PMCID: PMC5444767          DOI: 10.18632/oncotarget.15739

Source DB:  PubMed          Journal:  Oncotarget        ISSN: 1949-2553


  35 in total

1.  Quantifying heterogeneity in a meta-analysis.

Authors:  Julian P T Higgins; Simon G Thompson
Journal:  Stat Med       Date:  2002-06-15       Impact factor: 2.373

2.  Meta-analysis in clinical trials.

Authors:  R DerSimonian; N Laird
Journal:  Control Clin Trials       Date:  1986-09

Review 3.  BRCA1 and its toolbox for the maintenance of genome integrity.

Authors:  Michael S Y Huen; Shirley M H Sy; Junjie Chen
Journal:  Nat Rev Mol Cell Biol       Date:  2009-12-23       Impact factor: 94.444

4.  Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population.

Authors:  A M Dunning; M Chiano; N R Smith; J Dearden; M Gore; S Oakes; C Wilson; M Stratton; J Peto; D Easton; D Clayton; B A Ponder
Journal:  Hum Mol Genet       Date:  1997-02       Impact factor: 6.150

5.  A functional BRCA1 coding sequence genetic variant contributes to risk of esophageal squamous cell carcinoma.

Authors:  Xiaojiao Zhang; Jinyu Wei; Liqing Zhou; Changchun Zhou; Juan Shi; Qipeng Yuan; Ming Yang; Dongxin Lin
Journal:  Carcinogenesis       Date:  2013-06-08       Impact factor: 4.944

6.  Lack of association of BRCA1 and BRCA2 variants with breast cancer in an ethnic population of Saudi Arabia, an emerging high-risk area.

Authors:  Tarique Noorul Hasan; Gowhar Shafi; Naveed Ahmed Syed; Mohammed Abdullah Alsaif; Abdulaziz Abdullah Alsaif; Ali Abdullah Alshatwi
Journal:  Asian Pac J Cancer Prev       Date:  2013

Review 7.  Mechanisms of human DNA repair: an update.

Authors:  Markus Christmann; Maja T Tomicic; Wynand P Roos; Bernd Kaina
Journal:  Toxicology       Date:  2003-11-15       Impact factor: 4.221

8.  A polymorphism in Werner syndrome gene is associated with breast cancer susceptibility in Chinese women.

Authors:  Zhanwei Wang; Yan Xu; Jinhai Tang; Hongxia Ma; Jianwei Qin; Chen Lu; Xuechen Wang; Zhibin Hu; Xinru Wang; Hongbing Shen
Journal:  Breast Cancer Res Treat       Date:  2009-02-10       Impact factor: 4.872

9.  Polymorphisms in BRCA1, BRCA1-interacting genes and susceptibility of breast cancer in Chinese women.

Authors:  Xiang Huo; Cheng Lu; Xinen Huang; Zhibin Hu; Guangfu Jin; Hongxia Ma; Xuechen Wang; Jianwei Qin; Xinru Wang; Hongbing Shen; Jinhai Tang
Journal:  J Cancer Res Clin Oncol       Date:  2009-05-31       Impact factor: 4.553

10.  BRCA1 induces DNA damage recognition factors and enhances nucleotide excision repair.

Authors:  Anne-Renee Hartman; James M Ford
Journal:  Nat Genet       Date:  2002-08-26       Impact factor: 38.330

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