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利用高通量单核苷酸多态性基因分型技术在查谟和克什米尔人群中进行结直肠癌的遗传分析。

Genetic analysis of colorectal carcinoma using high throughput single nucleotide polymorphism genotyping technique within the population of Jammu and Kashmir.

机构信息

School of Biotechnology, Shri Mata Vaishno Devi University, Jammu and Kashmir 182320, Katra, India.

Government Medical College Jammu, Jammu, 180001, India.

出版信息

Mol Biol Rep. 2021 Aug;48(8):5889-5895. doi: 10.1007/s11033-021-06583-8. Epub 2021 Jul 28.

Abstract

BACKGROUND

SNP genotyping has become increasingly more common place to understand the genetic basis of complex diseases like cancer. SNP-genotyping through MassARRAY™ is a cost-effective method to quantitatively analyse the variation of gene expression in multiple samples, making it a potential tool to identify the underlying causes of colorectal carcinogenesis.

METHODS

In the present study, SNP genotyping was carried out using Agena MassARRAY™, which is a cost-effective, robust, and sensitive method to analyse multiple SNPs simultaneously. We analysed 7 genes in 492 samples (100 cases and 392 controls) associated with CRC within the population of Jammu and Kashmir. These SNPs were selected based on their association with multiple cancers in literature.

RESULTS

This is the first study to explore these SNPs with colorectal cancer within the J&K population.7 SNPs with a call rate of 90% were selected for the study. Out of these, five SNPs rs2234593, rs1799966, rs2229080, rs8034191, rs1042522 were found to be significantly associated with the current study under the allelic model with an Odds Ratio OR = 2.981(1.731-5.136 at 95% CI); p value = 4.81E-05 for rs2234593,OR = 1.685(1.073-2.647 at 95% CI);; p value = 0.02292 for rs1799966, OR = 1.5 (1.1-2.3 at 95% CI), p value = 0.02 for rs2229080, OR = 1.699(1.035-2.791 at 95% CI); p value = 0.03521 for rs8034191, OR = 20.07 (11.26-35.75); p value = 1.84E-34 for rs1042522 respectively.

CONCLUSION

This is the first study to find the relation of Genetic variants with the colorectal cancer within the studied population using high throughput MassARRAY™ technology. It is further anticipated that the variants should be evaluated in other population groups that may aid in understanding the genetic complexity and bridge the missing heritability.

摘要

背景

SNP 基因分型已成为了解癌症等复杂疾病遗传基础的一种越来越常见的方法。通过 MassARRAY™ 进行 SNP 基因分型是一种经济有效的方法,可以定量分析多个样本中基因表达的变化,使其成为识别结直肠癌发生潜在原因的潜在工具。

方法

本研究采用 Agena MassARRAY™ 进行 SNP 基因分型,这是一种经济高效、稳健且敏感的同时分析多个 SNP 的方法。我们分析了在查谟和克什米尔人群中与 CRC 相关的 7 个基因中的 492 个样本(100 例病例和 392 例对照)中的 SNP。这些 SNP 是根据它们与文献中多种癌症的关联选择的。

结果

这是第一项在 J&K 人群中探讨这些 SNP 与结直肠癌关系的研究。选择了 7 个具有 90%呼叫率的 SNP 进行研究。其中,rs2234593、rs1799966、rs2229080、rs8034191、rs1042522 这 5 个 SNP 在等位基因模型下与当前研究显著相关,优势比(OR)为 2.981(95%置信区间为 1.731-5.136);p 值=4.81E-05,rs2234593;OR=1.685(95%置信区间为 1.073-2.647);p 值=0.02292,rs1799966,OR=1.5(1.1-2.3),p 值=0.02,rs2229080,OR=1.699(95%置信区间为 1.035-2.791);p 值=0.03521,rs8034191,OR=20.07(11.26-35.75);p 值=1.84E-34,rs1042522。

结论

这是第一项使用高通量 MassARRAY™ 技术在研究人群中发现遗传变异与结直肠癌关系的研究。进一步预计,应在其他人群中评估这些变体,这可能有助于理解遗传复杂性并弥合缺失的遗传率。

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