首页> 美国卫生研究院文献>Journal of Cancer Epidemiology >Role of GSTM1 and GSTT1 Gene Polymorphisms on Lung Cancer Susceptibility and Effect on Platinum-Based Chemotherapy-Induced Toxicity in Bangladeshi Lung Cancer Patients
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Role of GSTM1 and GSTT1 Gene Polymorphisms on Lung Cancer Susceptibility and Effect on Platinum-Based Chemotherapy-Induced Toxicity in Bangladeshi Lung Cancer Patients

机译:GSTM1 和 GSTT1 基因多态性对孟加拉国肺癌患者肺癌易感性的影响及其对铂类化疗诱导毒性的影响

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摘要

Background: Glutathione S-transferases (GSTs) play a significant role in carcinogen detoxification, and hence, polymorphisms of this gene may lead to lung cancer susceptibility. Accordingly, this study is aimed at investigating GSTM1 and GSTT1 polymorphisms' association with lung cancer risk and their effects on the toxicities of platinum-based chemotherapy used to treat Bangladeshi lung cancer patients. Methods: The study subjects comprised 180 lung cancer patients and 200 healthy volunteers. Genetic polymorphisms of GSTM1 and GSTT1 were analyzed using a multiplex PCR–based method. Chemotherapy toxicity was evaluated using the Common Terminology Criteria for Adverse Events (CTCAE v5.0). Results: GSTM1 null genotype was found to be significantly associated with a 1.6-fold increased risk of lung cancer (OR = 1.60, 95%CI = 1.01–2.52, p = 0.0491), whereas no significant association was observed with GSTT1 null genotype and combined GSTM1 and GSTT1 null genotype. Moreover, no significant relationship was observed between GSTM1 and GSTT1 polymorphisms and the increased risk of platinum-based chemotherapy-induced toxicities in lung cancer patients. Conclusions: These findings indicated that the GSTM1 null but not GSTT1 null genotype was significantly associated with lung cancer susceptibility. These polymorphisms were not related to platinum-based chemotherapy-induced toxicities in Bangladeshi lung cancer patients.
机译:背景: 谷胱甘肽 S-转移酶 (GSTs) 在致癌物解毒中起重要作用,因此,该基因的多态性可能导致肺癌易感性。因此,本研究旨在调查 GSTM1 和 GSTT1 多态性与肺癌风险的关系及其对用于治疗孟加拉国肺癌患者的铂类化疗毒性的影响。方法: 研究对象包括 180 例肺癌患者和 200 例健康志愿者。使用基于多重 PCR 的方法分析 GSTM1 和 GSTT1 的遗传多态性。使用不良事件通用术语标准 (CTCAE v5.0) 评估化疗毒性。结果:发现 GSTM1 无效基因型与肺癌风险增加 1.6 倍显著相关 (OR = 1.60,95%CI = 1.01–2.52,p = 0.0491),而未观察到与 GSTT1 无效基因型以及 GSTM1 和 GSTT1 联合无效基因型的显著关联。此外,在肺癌患者中,未观察到 GSTM1 和 GSTT1 多态性与铂类化疗诱导的毒性风险增加之间存在显着关系。结论: 这些发现表明 GSTM1 无效基因型而非 GSTT1 无效基因型与肺癌易感性显著相关。这些多态性与孟加拉国肺癌患者铂类化疗诱导的毒性无关。

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