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

IF 1 4区 生物学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Genes & genetic systems Pub Date : 2021-12-16 Epub Date: 2021-11-19 DOI:10.1266/ggs.21-00010
Bhanu Sharma, Shabab Angurana, Ruchi Shah, Sonali Verma, Amrita Bhat, G R Bhat, Divya Bakshi, Rajeshwer Singh Jamwal, Mukesh Tanwar, Supinder Singh, Audesh Bhat, Samantha Vaishnavi, Rakesh Kumar
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引用次数: 3

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.

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ARID5B与印度查谟和克什米尔地区结直肠癌风险的遗传关联
结直肠癌(CRC),包括从结肠或直肠发展而来的癌症,是印度查谟和克什米尔(J&K)人口中高度流行的癌症之一。然而,在这一人群中缺乏CRC的病例-对照遗传关联研究。先前的各种全基因组关联研究表明,位于染色体10q21.2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)在结直肠癌的发生中起着重要作用。在印度北部人群中,ARID5B与结直肠癌风险之间的关系尚不清楚。为了了解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,研究ARID5B的癌症易感变异rs10740055与J&K人群结直肠癌的关系。该研究包括180例病例和390名健康对照。采用TaqMan检测技术对rs10740055变异进行RT-PCR分型。采用卡方检验评估变异的Hardy-Weinberg平衡。等位基因和基因型特异性风险通过比值比(ORs)估算,置信区间为95%。rs10740055变异显示出更高的结直肠癌风险,OR为3.35 (95% CI为1.99-5.65),校正年龄、性别、种族、BMI、饮酒和吸烟后P = 0.000005。我们的结果表明,rs10740055的A等位基因给人群带来了风险,需要更大的样本量进行进一步的统计验证。其他ARID家族基因中其他变异的相关性也应进行测试,因为它们的作用不能被排除。
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来源期刊
Genes & genetic systems
Genes & genetic systems 生物-生化与分子生物学
CiteScore
1.50
自引率
0.00%
发文量
22
审稿时长
>12 weeks
期刊介绍: Genes & Genetic Systems , formerly the Japanese Journal of Genetics , is published bimonthly by the Genetics Society of Japan.
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