长还是短?端粒长度与胰腺癌及其前体病变的关系。

IF 2.5 4区 医学 Q3 GENETICS & HEREDITY
Mutagenesis Pub Date : 2023-11-17 DOI:10.1093/mutage/gead034
Daniele Campa, Alessio Felici, Chiara Corradi, Giulia Peduzzi, Manuel Gentiluomo, Riccardo Farinella, Cosmeri Rizzato
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引用次数: 0

摘要

胰腺导管腺癌(PDAC)是最常见和最致命的胰腺癌,诊断后5年生存率接近11%。在过去的15年中,端粒长度在白细胞(LTL)测量已研究与PDAC风险。大多数研究报告了较短的LTL与PDAC风险增加之间的关联,但结果是不一致的。全基因组关联研究已经确定端粒酶逆转录酶(TERT)基因中的几个单核苷酸多态性(snp)是PDAC的易感位点。使用与LTL相关的snp计算的多基因风险评分(PRS)已经用各种方法测试了与PDAC易感性的关系,并给出了对比的结果。本综述的目的是分析所有专门针对LTL的出版物,考虑到用qPCR和遗传代理测量的LTL,以及PDAC风险。此外,我们将概述端粒相关基因中snp与PDAC之间最相关的关联,以回答短或长?两者中哪一个与PDAC风险相关?
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Long or short? Telomere length and pancreatic cancer and its precursor lesions, a narrative review.

Pancreatic ductal adenocarcinoma (PDAC) is the most common and lethal form of pancreatic cancer, with a survival approaching only 11% at five years after diagnosis. In the last 15 years, telomere length measured in leukocyte (LTL) has been studied in relation to PDAC risk. The majority of the studies reported an association between short LTL and increased PDAC risk, but the results are heterogeneous. Genome-wide association studies have identified several single nucleotide polymorphisms (SNPs) in the telomerase reverse transcriptase (TERT) gene as susceptibility loci for PDAC. Polygenic risk scores (PRS) computed using SNPs associated with LTL have been tested in relation to PDAC susceptibility with various methods and giving contrasting results. The aim of this review is to analyze all publications carried out specifically on LTL, considering LTL measured with qPCR and with genetic proxies, and PDAC risk. Additionally, we will give an overview of the most relevant associations between SNPs in telomere associated genes and PDAC, to answer the question shorter or longer? Which one of the two is associated with PDAC risk?

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来源期刊
Mutagenesis
Mutagenesis 生物-毒理学
CiteScore
5.90
自引率
3.70%
发文量
22
审稿时长
6-12 weeks
期刊介绍: Mutagenesis is an international multi-disciplinary journal designed to bring together research aimed at the identification, characterization and elucidation of the mechanisms of action of physical, chemical and biological agents capable of producing genetic change in living organisms and the study of the consequences of such changes.
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