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印度查谟和克什米尔地区ARID5B与结直肠癌风险的遗传关联。

Genetic association of ARID5B with the risk of colorectal cancer within Jammu and Kashmir, India.

作者信息

Sharma Bhanu, Angurana Shabab, Shah Ruchi, Verma Sonali, Bhat Amrita, Bhat G R, Bakshi Divya, Jamwal Rajeshwer Singh, Tanwar Mukesh, Singh Supinder, Bhat Audesh, Vaishnavi Samantha, Kumar Rakesh

机构信息

School of Biotechnology, Shri Mata Vaishno Devi University.

Department of Radiotherapy, Government Medical College.

出版信息

Genes Genet Syst. 2021 Dec 16;96(4):187-191. doi: 10.1266/ggs.21-00010. Epub 2021 Nov 19.

Abstract

Colorectal cancer (CRC), which includes the development of cancer from the colon or rectum, is one of the highly prevalent cancers in the populations of Jammu and Kashmir (J&K) in India. However, case-control genetic association studies on CRC are lacking in this population. Various genome-wide association studies have previously shown that single-nucleotide polymorphisms (SNPs) of the AT-rich interaction domain 5B (ARID5B) gene located on chromosome 10q21.2 contribute substantially to the development of colorectal cancer. The association between ARID5B and CRC risk in north Indian population groups is still unknown. To understand the role of ARID5B SNPs in CRC in the population of J&K, we designed a case-control study to investigate the association of the cancer susceptibility variant rs10740055 of ARID5B with CRC in the population of J&K. The study included 180 cases and 390 healthy controls. Genotyping of the rs10740055 variant was performed by RT-PCR using the TaqMan assay technique. Hardy-Weinberg equilibrium of the variant was assessed using the chi-squared test. The allele- and genotype-specific risks were estimated by odds ratios (ORs) with 95% confidence intervals (CIs). The rs10740055 variant showed a higher risk for colorectal cancer with an OR of 3.35 (1.99-5.65 at 95% CI) and P = 0.000005 corrected for age, gender, ethnicity, BMI, alcohol intake and smoking. Our results indicate that the A allele of rs10740055 imparts risk to the population and also that a larger sample size is needed for further statistical validation. The association of other variants in other ARID family genes should also be tested as their role cannot be ruled out.

摘要

结直肠癌(CRC),包括结肠癌或直肠癌的癌变,是印度查谟和克什米尔(J&K)地区人群中高度流行的癌症之一。然而,该人群缺乏关于结直肠癌的病例对照基因关联研究。此前多项全基因组关联研究表明,位于10q21.2染色体上的富含AT的相互作用结构域5B(ARID5B)基因的单核苷酸多态性(SNP)对结直肠癌的发生有重大影响。ARID5B与印度北部人群结直肠癌风险之间的关联仍不清楚。为了解ARID5B SNP在J&K人群结直肠癌中的作用,我们设计了一项病例对照研究,以调查ARID5B的癌症易感性变异rs10740055与J&K人群结直肠癌的关联。该研究纳入了180例病例和390名健康对照。使用TaqMan检测技术通过RT-PCR对rs10740055变异进行基因分型。使用卡方检验评估该变异的哈迪-温伯格平衡。通过比值比(OR)及95%置信区间(CI)估计等位基因和基因型特异性风险。rs10740055变异显示出较高的结直肠癌风险,OR为3.35(95%CI为1.99 - 5.65),校正年龄、性别、种族、BMI、酒精摄入和吸烟因素后P = 0.000005。我们的结果表明,rs10740055的A等位基因使人群具有患病风险,并且还需要更大的样本量进行进一步的统计学验证。其他ARID家族基因中其他变异的关联也应进行检测,因为不能排除它们的作用。

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