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谷胱甘肽硫转移酶 M1 和 T1 基因插入/缺失多态性与结直肠癌风险的关联:巴基斯坦开伯尔-普赫图赫瓦省人群的病例对照研究。

Association of GSTM1 and GSTT1 genes insertion/deletion polymorphism with colorectal cancer risk: A case-control study of Khyber Pakhtunkhwa population, Pakistan.

机构信息

Department of Biochemistry, Institute of Chemical Sciences, University of Peshawar, Peshawar, Pakistan.

Department of Surgery, Khyber Teaching Hospital, Peshawar, Pakistan.

出版信息

J Pak Med Assoc. 2022 Mar;72(3):457-463. doi: 10.47391/JPMA.1393.

Abstract

OBJECTIVE

To evaluate the genetic association of glutathione S transferase M1 and glutathione S transferase T1 genes insertion/deletion polymorphism with the risk of colorectal cancer.

METHODS

This case-control study was conducted March 2018 and November 2019 at the University of Peshawar, Peshawar, Pakistan, and comprised blood samples from colorectal cancer patients and age- and gender-matched controls. Deoxyribonucleic acid was extracted from blood samples, and glutathione S transferase M1 and glutathione S transferase T1 genotyping was performed using polymerase chain reaction at the Institute of Radiation and Nuclear Medicine, Peshawar. Data regarding age, gender, location, smoking status, cancer stage and node involvement was collected on a predesigned proforma. Data was analysed using Minitab 17.

RESULTS

The frequency of glutathione S transferase M1 was was significantly associated with colorectal cancer risk (p<0.01), while glutathione S transferase T1 null genotype showed non-significant association (p<0.43). The association between the combined deletion of glutathione S transferase M1 and glutathione S transferase T1 polymorphism and the colorectal risk was significant (p=0.011). Glutathione S transferase M1 and glutathione S transferase T1 deletions had non-significant association with age, smoking status, dwelling and tumour location (p>0.05) when compared with the wild genotypes in colorectal cancer cases.

CONCLUSION

Glutathione S transferase M1 gene deletion was found to be associated with the risk of colorectal cancer development.

摘要

目的

评估谷胱甘肽 S-转移酶 M1 和谷胱甘肽 S-转移酶 T1 基因插入/缺失多态性与结直肠癌风险的遗传关联。

方法

本病例对照研究于 2018 年 3 月至 2019 年 11 月在巴基斯坦白沙瓦的白沙瓦大学进行,纳入了结直肠癌患者和年龄、性别匹配的对照的血液样本。从血液样本中提取脱氧核糖核酸,在白沙瓦的放射与核医学研究所使用聚合酶链反应进行谷胱甘肽 S-转移酶 M1 和谷胱甘肽 S-转移酶 T1 基因分型。使用预设计的表格收集了年龄、性别、位置、吸烟状况、癌症分期和淋巴结受累等数据。数据使用 Minitab 17 进行分析。

结果

谷胱甘肽 S-转移酶 M1 的频率与结直肠癌风险显著相关(p<0.01),而谷胱甘肽 S-转移酶 T1 无效基因型显示无显著相关性(p<0.43)。谷胱甘肽 S-转移酶 M1 和谷胱甘肽 S-转移酶 T1 多态性联合缺失与结直肠癌风险显著相关(p=0.011)。与野生基因型相比,谷胱甘肽 S-转移酶 M1 和谷胱甘肽 S-转移酶 T1 缺失在结直肠癌病例中与年龄、吸烟状况、居住和肿瘤位置无显著相关性(p>0.05)。

结论

谷胱甘肽 S-转移酶 M1 基因缺失与结直肠癌发生的风险相关。

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