Role of polymorphic XRCC6 (Ku70)/XRCC7 (DNA-PKcs) genes towards susceptibility and prognosis of lung cancer patients undergoing platinum based doublet chemotherapy

被引:0
|
作者
Amrita Singh
Navneet Singh
Digambar Behera
Siddharth Sharma
机构
[1] Thapar University,Department of Biotechnology
[2] Post Graduate Institute of Medical Education and Research (PGIMER),Department of Pulmonary Medicine
来源
Molecular Biology Reports | 2018年 / 45卷
关键词
Lung cancer; Susceptibility; Survival; Genotype; ADCC; SQCC; SCLC;
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学科分类号
摘要
The DNA repair genes XRCC6 and XRCC7 formed an integral part of double strand break repair (DSBR) pathway. The two genes are thought to play an important role in the repair of lethal double strand damage on DNA. Polymorphic DSBR genes are studied to effect genomic stability. We intend to explore the association of DSBR genes i.e. XRCC6 and XRCC7 with susceptibility and survival in North Indian lung cancer patients. DNA isolation and genotyping was done for 320 controls and 330 lung cancer cases enrolled in the study. Each and every lung cancer study subjects were made a telephonic call and were followed for their health after administration of chemotherapy. Statistical analysis for susceptibility was done using logistic regression analysis. Survival analysis was done using Kaplan–Meier followed by Cox-regression. Small cell lung cancer (SCLC) subtype posed an amplified risk towards lung cancer in case of XRCC7 6721G>T (OR = 4.11, p = 0.0040). Gene-environment interaction analysis revealed that non-smokers with heterozygous genotype (CG) in case of XRCC6 61C>G showed a strong protective effect (OR = 0.38, p = 0.01) towards lung cancer. Survival analysis revealed poor prognosis in case of XRCC6 61C>G SCLC subtype. XRCC6 and XRCC7 were not involved in overall susceptibility and survival. However, in case of XRCC7 6721G>T subjects with SCLC subtype showed an increased susceptibility while poor prognosis in case of XRCC6 61C>G.
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页码:253 / 261
页数:8
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    Singh, Amrita
    Singh, Navneet
    Behera, Digambar
    Sharma, Siddharth
    [J]. MOLECULAR BIOLOGY REPORTS, 2018, 45 (03) : 253 - 261
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