首页> 美国卫生研究院文献>International Journal of Molecular Sciences >The Role of Genetic Polymorphisms as Related to One-Carbon Metabolism Vitamin B6 and Gene–Nutrient Interactions in Maintaining Genomic Stability and Cell Viability in Chinese Breast Cancer Patients
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The Role of Genetic Polymorphisms as Related to One-Carbon Metabolism Vitamin B6 and Gene–Nutrient Interactions in Maintaining Genomic Stability and Cell Viability in Chinese Breast Cancer Patients

机译:遗传多态性与单碳代谢维生素B6和基因营养相互作用在维持中国乳腺癌患者基因组稳定性和细胞生存力中的作用

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摘要

Folate-mediated one-carbon metabolism (FMOCM) is linked to DNA synthesis, methylation, and cell proliferation. Vitamin B6 (B6) is a cofactor, and genetic polymorphisms of related key enzymes, such as serine hydroxymethyltransferase (SHMT), methionine synthase reductase (MTRR), and methionine synthase (MS), in FMOCM may govern the bioavailability of metabolites and play important roles in the maintenance of genomic stability and cell viability (GSACV). To evaluate the influences of B6, genetic polymorphisms of these enzymes, and gene–nutrient interactions on GSACV, we utilized the cytokinesis-block micronucleus assay (CBMN) and PCR-restriction fragment length polymorphism (PCR-RFLP) techniques in the lymphocytes from female breast cancer cases and controls. GSACV showed a significantly positive correlation with B6 concentration, and 48 nmol/L of B6 was the most suitable concentration for maintaining GSACV in vitro. The GSACV indexes showed significantly different sensitivity to B6 deficiency between cases and controls; the B6 effect on the GSACV variance contribution of each index was significantly higher than that of genetic polymorphisms and the sample state (tumor state). SHMT C1420T mutations may reduce breast cancer susceptibility, whereas MTRR A66G and MS A2756G mutations may increase breast cancer susceptibility. The role of SHMT, MS, and MTRR genotype polymorphisms in GSACV is reduced compared with that of B6. The results appear to suggest that the long-term lack of B6 under these conditions may increase genetic damage and cell injury and that individuals with various genotypes have different sensitivities to B6 deficiency. FMOCM metabolic enzyme gene polymorphism may be related to breast cancer susceptibility to a certain extent due to the effect of other factors such as stress, hormones, cancer therapies, psychological conditions, and diet. Adequate B6 intake may be good for maintaining genome health and preventing breast cancer.
机译:叶酸介导的一碳代谢(FMOCM)与DNA合成,甲基化和细胞增殖有关。维生素B6(B6)是辅助因子,FMOCM中相关关键酶的遗传多态性,例如丝氨酸羟甲基转移酶(SHMT),蛋氨酸合酶还原酶(MTRR)和蛋氨酸合酶(MS),可能控制代谢物的生物利用度并发挥重要作用在维持基因组稳定性和细胞活力(GSACV)中发挥重要作用。为了评估B6,这些酶的遗传多态性以及基因-营养相互作用对GSACV的影响,我们利用了女性淋巴细胞中的胞质阻滞微核试验(CBMN)和PCR限制性片段长度多态性(PCR-RFLP)技术乳腺癌病例和对照。 GSACV与B6浓度呈显着正相关,而48 nmol / L的B6是体外维持GSACV的最合适浓度。 GSACV指数显示病例与对照组之间对B6缺乏症的敏感性显着不同。 B6对每个指标的GSACV方差贡献的影响显着高于遗传多态性和样本状态(肿瘤状态)。 SHMT C1420T突变可能会降低乳腺癌的易感性,而MTRR A66G和MS A2756G突变可能会提高乳腺癌的易感性。与B6相比,GSACV中SHMT,MS和MTRR基因型多态性的作用降低。结果似乎表明,在这种情况下长期缺乏B6可能会增加遗传损伤和细胞损伤,并且具有不同基因型的个体对B6缺乏症的敏感性不同。 FMOCM代谢酶基因多态性在一定程度上可能与乳腺癌易感性有关,这是由于其他因素(例如压力,激素,癌症治疗,心理状况和饮食)的影响。摄入足够的B6可能对维持基因组健康和预防乳腺癌有好处。

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