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胸苷酸合成酶3'-非翻译区多态性与结直肠癌的患病率及预后

3'-UTR Polymorphisms in Thymidylate Synthase with Colorectal Cancer Prevalence and Prognosis.

作者信息

Jeon Young-Joo, Cho Sung-Hwan, Kim Eo-Jin, Ryu Chang-Soo, Park Han-Sung, Kim Jong-Woo, Lee Jeong-Yong, An Hui-Jeong, Kim Nam-Keun

机构信息

Department of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea.

Division of Hematology/Oncology, Department of Internal Medicine, Kangbuk Samsung Hospital, Sungkyunkwan University School of Medicine, Seoul 06351, Korea.

出版信息

J Pers Med. 2021 Jun 9;11(6):537. doi: 10.3390/jpm11060537.

Abstract

Colorectal cancer (CRC) is the third most common type of cancer and the second leading cause of cancer-related mortality in Western countries. Polymorphisms in one-carbon metabolism and angiogenesis-related genes have been shown to play important roles in tumor development, progression, and metastasis for many cancers, including CRC. Moreover, recent studies have reported that polymorphisms in specific microRNA (miRNA)-binding regions, which are located in the 3'-untranslated region (UTR) of miRNA-regulated genes, are present in a variety of cancers. Here, we investigated the association between two thymidylate synthase ( or 3'-UTR polymorphisms, 1100T>C [rs699517] and 1170A>G [rs2790], and CRC susceptibility and progression in Korean patients. A total of 450 CRC patients and 400 healthy controls were enrolled in this study, and genotyping at the TS locus was performed by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) or TaqMan allelic discrimination assays. We found that TS 1170A>G genotypes, as well as the TS 1100T-1170G and 1100C-1170A haplotypes, are strongly associated with CRC. The TS 1100TC+CC type was associated with a poor survival (OS and RFS) rate. In addition, levels of the TS 1100C and TS 1170G allele were found to be significantly increased in CRC tissue. Our study provides the first evidence for 3'-UTR variants in TS genes as potential biomarkers of CRC prognosis and prevention.

摘要

结直肠癌(CRC)是第三大常见癌症类型,也是西方国家癌症相关死亡的第二大主要原因。已表明,一碳代谢和血管生成相关基因的多态性在包括CRC在内的许多癌症的肿瘤发生、发展和转移中发挥重要作用。此外,最近的研究报告称,位于miRNA调控基因3'非翻译区(UTR)的特定微小RNA(miRNA)结合区域存在多态性,这种多态性存在于多种癌症中。在此,我们研究了韩国患者中胸苷酸合成酶(TS)基因的两个3'UTR多态性,即1100T>C [rs699517]和1170A>G [rs2790]与CRC易感性及病情进展之间的关联。本研究共纳入450例CRC患者和400例健康对照,通过聚合酶链反应-限制性片段长度多态性(PCR-RFLP)或TaqMan等位基因鉴别分析对TS基因座进行基因分型。我们发现,TS 1170A>G基因型以及TS 1100T-1170G和1100C-1170A单倍型与CRC密切相关。TS 1100TC + CC型与较差的生存率(总生存期和无复发生存期)相关。此外,在CRC组织中发现TS 1100C和TS 1170G等位基因水平显著升高。我们的研究首次证明TS基因的3'UTR变异体是CRC预后和预防的潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4b34/8228787/12c861a069ef/jpm-11-00537-g001.jpg

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本文引用的文献

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