Literature DB >> 20411322

Haplotype analysis of XRCC1 (at codons 194 and 399) and susceptibility to breast cancer, a meta-analysis of the literatures.

Mostafa Saadat1.   

Abstract

To clarify the association between XRCC1 haplotypes and susceptibility to breast cancer, a meta-analysis of case-control studies were conducted. Eligible studies were identified by searching several databases for relevant reports published before March 2010. In total, 10 studies were included in the present meta-analysis. XRCC1 haplotypes for Arg194Trp and Arg399Gln polymorphisms were included in the analysis. The association was measured using random-effect model or fixed-effect model odds ratio (OR) combined with 95% confidence intervals (CIs) according to the between studies' heterogeneity. Large between-study heterogeneity was observed (Q = 25.587, df = 9, P < 0.001). The meta-analysis showed a borderline increased risk of breast cancer associated with the Arg194-Gln399 haplotype versus the Arg194-Arg399 haplotype (OR = 1.07, 95% CI: 1.01-1.14). There was no significant association between XRCC1 haplotypes and risk of breast cancer among Caucasoid subjects. In the next step, studies were classified according to geographical locations. Studies reported form Western populations did not show heterogeneity, and the Arg194-Gln399 haplotype was not associated with risk of breast cancer in comparison with the Arg194-Arg399 haplotype (OR = 1.02, 95% CI: 0.95-1.09). Among studies reported form Asian countries, significant heterogeneity was observed. After excluding of one study which did not show linkage disequilibrium, heterogeneity between studies decreased and haplotype Arg194-Gln399 revealed significant association with increased risk of breast cancer compared with haplotype Arg194-Arg399 (OR = 1.26, 95% CI: 1.04-1.50). There was no significant association between Trp194-Arg399 haplotype and risk of breast cancer, neither in Western nor Asian countries. The present meta-analysis has indicated that the Arg194-Gln399 haplotype of XRCC1 might be a risk factor for breast cancer in Asian countries.

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Year:  2010        PMID: 20411322     DOI: 10.1007/s10549-010-0895-y

Source DB:  PubMed          Journal:  Breast Cancer Res Treat        ISSN: 0167-6806            Impact factor:   4.872


  10 in total

1.  XRCC1 R399Q polymorphism and risk of normal tissue injury after radiotherapy in breast cancer patients.

Authors:  Yingying Zhou; Weibing Zhou; Qiong Liu; Zhiru Fan; Zhen Yang; Qingsong Tu; Li Li; Haifeng Liu
Journal:  Tumour Biol       Date:  2013-12-03

2.  Genetic polymorphisms in key DNA repair genes and risk of head and neck cancer in a Chinese population.

Authors:  Hua Yuan; Huizhang Li; Hongxia Ma; Yuming Niu; Yunong Wu; Shangyue Zhang; Zhibin Hu; Hongbing Shen; Ning Chen
Journal:  Exp Ther Med       Date:  2012-02-09       Impact factor: 2.447

3.  Association between polymorphisms at promoters of XRCC5 and XRCC6 genes and risk of breast cancer.

Authors:  Mehrdad Rajaei; Iraj Saadat; Shahpour Omidvari; Mostafa Saadat
Journal:  Med Oncol       Date:  2014-03-11       Impact factor: 3.064

4.  Association between N142D genetic polymorphism of GSTO2 and susceptibility to colorectal cancer.

Authors:  Mohammad Masoudi; Iraj Saadat; Shahpour Omidvari; Mostafa Saadat
Journal:  Mol Biol Rep       Date:  2010-11-27       Impact factor: 2.316

Review 5.  Polymorphisms in base excision repair genes: Breast cancer risk and individual radiosensitivity.

Authors:  Clarice Patrono; Silvia Sterpone; Antonella Testa; Renata Cozzi
Journal:  World J Clin Oncol       Date:  2014-12-10

6.  Association between polymorphisms of XRCC1, p53 and MDR1 genes, the expression of their protein products and prognostic significance in human breast cancer.

Authors:  Silvia Rybárová; Janka Vecanová; Ingrid Hodorová; Jozef Mihalik; Martina Čižmáriková; Ján Mojžiš; Peter Solár; Marián Benický; Marian Adamkov; Ladislav Mirossay
Journal:  Med Sci Monit       Date:  2011-12

7.  TP53 and XRCC1 polymorphisms and breast cancer prognosis: a case-case study.

Authors:  Marina Silva Rodrigues; Camila Almeida Machado; Dante Pagnoncelli; Elizabeth Avvad; Júlio César da Paixão; Claudia Vitoria de Moura Gallo
Journal:  Clinics (Sao Paulo)       Date:  2011       Impact factor: 2.365

8.  Single nucleotide polymorphisms (SNPs) of ERCC2, hOGG1, and XRCC1 DNA repair genes and the risk of triple-negative breast cancer in Polish women.

Authors:  Beata Smolarz; Marianna Makowska; Dariusz Samulak; Magdalena M Michalska; Ewa Mojs; Maciej Wilczak; Hanna Romanowicz
Journal:  Tumour Biol       Date:  2014-01-09

9.  Association between ABO and Rh Blood Groups and Risk of Preeclampsia: A Case-Control Study from Iran.

Authors:  Firoozeh Aghasadeghi; Mostafa Saadat
Journal:  Open Access Maced J Med Sci       Date:  2017-01-14

10.  Susceptibility to preeclampsia is associated with a 50-bp insertion/deletion polymorphism at the promoter region of the SOD1 gene

Authors:  Somayeh Namdari; Mostafa Saadat
Journal:  J Turk Ger Gynecol Assoc       Date:  2021-12-06
  10 in total

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