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印度东部地区头颈部癌症患者 GSTM1 和 T1 基因缺失多态性的基因组模式。

Genomic Pattern of GSTM1 and T1 Gene Null polymorphism of Head and Neck Cancer Patients in Eastern India.

机构信息

Department of Biochemistry, Indira Gandhi Institute of Medical Sciences Sheikhpura, Patna, Bihar, India.

出版信息

Asian Pac J Cancer Prev. 2022 Aug 1;23(8):2655-2659. doi: 10.31557/APJCP.2022.23.8.2655.

Abstract

OBJECTIVE

Homozygous deletion i.e., null polymorphism of the Glutathione S transferases genes hinders detoxification reactions by altering the sensitization of glutathione s transferases enzymes. Hence, we analysed the association between the GSTM1 and GSTT1 gene polymorphisms and head and neck cancer (HNC).

METHODS

The study consists of 238 healthy controls and 160 diagnosed cases of HNC, who attended the Regional Cancer Centre, Indira Gandhi Institute of Medical Sciences (a tertiary care hospital). DNA was extracted from whole blood of patients and control using Qiagen DNA extraction kit. GSTM1 and GSTT1 gene polymorphisms were examined using PCR and agarose gel electrophoresis.

RESULTS

GSTM0 null polymorphism was 26.25% and 15.13% in cases and control respectively. GSTT0 null polymorphism was observed in 18.13% cases and 8.82% in control groups. The GSTM0 null polymorphism was present significantly in case group as compared to control group (OR = 1.997, p = 0.006). There was also significant association of GSTT0 null polymorphism with case group as compared to control group (OR = 2.288, p = 0.006). The combined genotypes were also analysed. GSTM0T1 genotype (n = 27) was found to be most common among HNC group followed next by GSTM0T0 double deletion (n =15).

CONCLUSION

The result indicated that there was strong association of GSTM0 and GSTT0 null polymorphism in those patients. The combined genotypes i.e., GSTM0T1 and GSTM0T0 null polymorphism also showed significant association in HNC patients.

摘要

目的

谷胱甘肽 S-转移酶基因的纯合缺失(即无效多态性)通过改变谷胱甘肽 S-转移酶的敏化作用,阻碍解毒反应。因此,我们分析了 GSTM1 和 GSTT1 基因多态性与头颈部癌症(HNC)之间的关联。

方法

该研究包括 238 名健康对照者和 160 名被诊断为 HNC 的患者,他们在地区癌症中心、英迪拉甘地医学科学研究所(三级保健医院)就诊。使用 Qiagen DNA 提取试剂盒从患者和对照者的全血中提取 DNA。使用 PCR 和琼脂糖凝胶电泳检查 GSTM1 和 GSTT1 基因多态性。

结果

GSTM0 无效多态性在病例组和对照组中分别为 26.25%和 15.13%。GSTT0 无效多态性在病例组中为 18.13%,在对照组中为 8.82%。与对照组相比,病例组中 GSTM0 无效多态性明显更为常见(OR = 1.997,p = 0.006)。GSTT0 无效多态性与病例组相比与对照组相比也存在显著关联(OR = 2.288,p = 0.006)。还分析了组合基因型。在 HNC 组中,GSTM0T1 基因型(n = 27)最为常见,其次是 GSTM0T0 双重缺失(n = 15)。

结论

结果表明,这些患者的 GSTM0 和 GSTT0 无效多态性存在很强的关联。在 HNC 患者中,联合基因型(即 GSTM0T1 和 GSTM0T0 无效多态性)也显示出显著的关联。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1975/9741883/0f63a6274895/APJCP-23-2655-g001.jpg

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