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ABCG 转运蛋白表达数量性状基因座与 5-FU 治疗的结直肠癌患者的生存相关。

Expression quantitative trait loci in ABC transporters are associated with survival in 5-FU treated colorectal cancer patients.

机构信息

Department of Molecular Biology of Cancer, Institute of Experimental Medicine, Prague, Czech Republic.

Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University, Prague, Czech Republic.

出版信息

Mutagenesis. 2020 Jul 11;35(3):273-281. doi: 10.1093/mutage/gez050.

DOI:10.1093/mutage/gez050
PMID:31922572
Abstract

The chemotherapeutic efficacy in colorectal cancer (CRC) is limited due to the inter-individual variability in drug response and the development of tumour resistance. ATP-binding cassette (ABC) transporters are crucial in the development of resistance by the efflux of anticancer agents from cancer cells. In this study, we identified 14 single nucleotide polymorphisms (SNPs) in 11 ABC transporter genes acting as an expression of quantitative trait loci (eQTLs), i.e. whose variation influence the expression of many downstream genes. These SNPs were genotyped in a case-control study comprising 1098 cases and 1442 healthy controls and analysed in relation to CRC development risk and patient survival. Considering a strict correction for multiple tests, we did not observe any significant association between SNPs and CRC risk. The rs3819720 polymorphism in the ABCB3/TAP2 gene was statistically significantly associated with shorter overall survival (OS) in the codominant, and dominant models [GA vs. GG, hazard ratio (HR) = 1.48; P = 0.002; AA vs. GG, HR = 1.70; P = 0.004 and GA + AA vs. GG, HR = 1.52; P = 0.0006]. Additionally, GA carriers of the same SNP displayed worse OS after receiving 5-FU based chemotherapy. The variant allele of rs3819720 polymorphism statistically significantly affected the expression of 36 downstream genes. Screening for eQTL polymorphisms in relevant genes such as ABC transporters that can regulate the expression of several other genes may help to identify the genetic background involved in the individual response to the treatment of CRC patients.

摘要

由于药物反应的个体间变异性和肿瘤耐药性的发展,结直肠癌 (CRC) 的化疗疗效有限。ATP 结合盒 (ABC) 转运蛋白在癌细胞中通过将抗癌药物排出细胞来抵抗药物方面起着至关重要的作用。在这项研究中,我们确定了 11 个 ABC 转运蛋白基因中的 14 个单核苷酸多态性 (SNP),这些 SNP 作为数量性状基因座 (eQTL) 的表达,即其变异影响许多下游基因的表达。这些 SNP 在包含 1098 例病例和 1442 例健康对照的病例对照研究中进行了基因分型,并分析了它们与 CRC 发展风险和患者生存的关系。考虑到对多次测试的严格校正,我们没有观察到 SNP 与 CRC 风险之间存在任何显著关联。ABCB3/TAP2 基因中的 rs3819720 多态性在共显性和显性模型中与总生存期 (OS) 较短具有统计学显著相关性[GA 与 GG,风险比 (HR) = 1.48;P = 0.002;AA 与 GG,HR = 1.70;P = 0.004 和 GA + AA 与 GG,HR = 1.52;P = 0.0006]。此外,相同 SNP 的 GA 携带者在接受基于 5-FU 的化疗后 OS 更差。rs3819720 多态性的变异等位基因统计学显著影响 36 个下游基因的表达。筛选与 ABC 转运蛋白等相关基因中的 eQTL 多态性,这些基因可以调节几个其他基因的表达,可能有助于识别涉及 CRC 患者个体对治疗反应的遗传背景。

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