首页> 美国卫生研究院文献>Technology in Cancer Research Treatment >DNA Repair Mechanism Gene XRCC1A (Arg194Trp) but not XRCC3 (Thr241Met) Polymorphism Increased the Risk of Breast Cancer in Premenopausal Females: A Case–Control Study in Northeastern Region of India
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DNA Repair Mechanism Gene XRCC1A (Arg194Trp) but not XRCC3 (Thr241Met) Polymorphism Increased the Risk of Breast Cancer in Premenopausal Females: A Case–Control Study in Northeastern Region of India

机译:DNA修复机制基因XRCC1A(Arg194Trp)而不是XRCC3(Thr241Met)多态性增加了绝经前女性患乳腺癌的风险:一项印度东北地区的病例对照研究

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摘要

X-ray repair cross complementary group gene is one of the most studied candidate gene involved in different types of cancers. Studies have shown that X-ray repair cross complementary genes are significantly associated with increased risk of breast cancer in females. Moreover, studies have revealed that X-ray repair cross complementary gene polymorphism significantly varies between and within different ethnic groups globally. The present case–control study was aimed to investigate the association of X-ray repair cross complementary 1A (Arg194Trp) and X-ray repair cross complementary 3 (Thr241Met) polymorphism with the risk of breast cancer in females from northeastern region of India. The present case–control study includes histopathologically confirmed and newly diagnosed 464 cases with breast cancer and 534 apparently healthy neighborhood community controls. Information on sociodemographic factors and putative risk factors were collected from each study participant by conducting face-to-face interviews. Genotyping of X-ray repair cross complementary 1A (Arg194Trp) and X-ray repair cross complementary 3 (Thr241Met) was carried out by polymerase chain reaction-restriction fragment length polymorphism. For statistical analysis, both univariate and multivariate logistic regression analyses were performed. We also performed stratified analysis to find out the association of X-ray repair cross complementary genes with the risk of breast cancer stratified based on menstrual status. This study revealed that tryptophan allele (R/W-W/W genotype) in X-ray repair cross complementary 1A (Arg194Trp) gene significantly increased the risk of breast cancer (adjusted odds ratio = 1.44, 95% confidence interval = 1.06-1.97, P < .05 for R/W-W/W genotype). Moreover, it was found that tryptophan allele (W/W genotype) at codon 194 of X-ray repair cross complementary 1A (Arg194Trp) gene significantly increased the risk of breast cancer in premenopausal females (crude odds ratio = 1.66, 95% confidence interval = 1.11-2.46, P < .05 for R/W-W/W genotype). The present study did not reveal any significant association of X-ray repair cross complementary 3 (Thr241Met) polymorphism with the risk of breast cancer. The present study has explored that X-ray repair cross complementary 1A (Arg194Trp) gene polymorphism is significantly associated with the increased risk of breast cancer in premenopausal females from northeastern region of India which may be beneficial for prognostic purposes.
机译:X射线修复交叉互补基团基因是涉及不同类型癌症的研究最多的候选基因之一。研究表明,X射线修复交叉互补基因与女性患乳腺癌的风险增加显着相关。此外,研究表明,X射线修复交叉互补基因多态性在全球不同种族之间和内部存在显着差异。本病例对照研究旨在调查印度东北地区女性的X射线修复交叉互补1A(Arg194Trp)和X射线修复交叉互补3(Thr241Met)多态性与乳腺癌风险的关系。本病例对照研究包括464例经组织病理学确诊和新诊断的乳腺癌患者以及534例显然健康的社区居民对照。通过进行面对面访谈从每个研究参与者那里收集有关社会人口统计学因素和推定风险因素的信息。通过聚合酶链反应-限制性片段长度多态性进行X射线修复交叉互补1A(Arg194Trp)和X射线修复交叉互补3(Thr241Met)的基因分型。为了进行统计分析,执行了单变量和多元逻辑回归分析。我们还进行了分层分析,以找出X射线修复交叉互补基因与基于月经状况进行分层的乳腺癌风险之间的关系。这项研究表明,X射线修复交叉互补1A(Arg194Trp)基因中的色氨酸等位基因(R / WW / W基因型)显着增加了罹患乳腺癌的风险(校正比值比= 1.44、95%置信区间= 1.6-1.97,P对于R / WW / W基因型,<.05)。此外,还发现X射线修复交叉互补1A(Arg194Trp)基因第194密码子的色氨酸等位基因(W / W基因型)显着增加了绝经前女性罹患乳腺癌的风险(原始优势比= 1.66,置信区间为95%) = 1.11-2.46,对于R / WW / W基因型,P <.05)。本研究未发现X射线修复交叉互补3(Thr241Met)多态性与患乳腺癌的风险之间存在显着关联。本研究探索了印度东北地区绝经前女性的X射线修复交叉互补1A(Arg194Trp)基因多态性与乳腺癌风险增加显着相关,这可能对预后有帮助。

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