Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/178839
Title: A genetic variant in telomerase reverse transcriptase (TERT) modifies cancer risk in Lynch syndrome patients harbouring pathogenic MSH2 variants
Author: Unhjem Wiik, Mariann
Evans, Tiffany Jane
Belhadj, Sami
Bolton, Katherine A.
Dymerska, Dagmara
Jagmohan Changur, Shantie
Capellá, G. (Gabriel)
Kurzawski, Grzegorz
Wijnen, Juul T.
Valle, Laura
Vasen, Hans F. A.
Lubinski, Jan
Scott, Rodney J.
Talseth Palmer, Bente A.
Keywords: Cancer
Malalties hereditàries
Factors de risc en les malalties
Càncer
Genetic diseases
Risk factors in diseases
Issue Date: 31-May-2021
Publisher: Springer Science and Business Media LLC
Abstract: Individuals with Lynch syndrome (LS), have an increased risk of developing cancer. Common genetic variants of telomerase reverse transcriptase (TERT) have been associated with a wide range of cancers, including colorectal cancer (CRC) in LS. We combined genotype data from 1881 LS patients, carrying pathogenic variants in MLH1, MSH2 or MSH6, for rs2075786 (G>A, intronic variant), 1207 LS patients for rs2736108 (C>T, upstream variant) and 1201 LS patients for rs7705526 (C>A, intronic variant). The risk of cancer was estimated by heterozygous/homozygous odds ratio (OR) with mixed-effects logistic regression to adjust for gene/gender/country of sample origin considering family identity. The AA genotype of SNP rs2075786 is associated with 85% higher odds at developing cancer compared to GG genotype in MSH2 pathogenic variant carriers (p = 0.0160). Kaplan-Meier analysis also shows an association for rs2075786; the AA allele for MSH2 variant carriers confers risk for earlier diagnosis of LS cancer (log-rank p = 0.0011). We report a polymorphism in TERT to be a possible modifier of disease risk in MSH2 pathogenic variant carriers. The rs2075786 SNP in TERT is associated with a differential risk of developing cancer for MSH2 pathogenic variant carriers. Use of this information has the potential to personalise screening protocols for LS patients.
Note: Reproducció del document publicat a: https://doi.org/10.1038/s41598-021-90501-2
It is part of: Scientific Reports, 2021, vol. 11, num. 11401
URI: http://hdl.handle.net/2445/178839
Related resource: https://doi.org/10.1038/s41598-021-90501-2
Appears in Collections:Articles publicats en revistes (Institut d'lnvestigació Biomèdica de Bellvitge (IDIBELL))

Files in This Item:
File Description SizeFormat 
s41598-021-90501-2.pdf1.32 MBAdobe PDFView/Open


This item is licensed under a Creative Commons License Creative Commons