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Telomere length assessment and molecular characterization of TERT gene promoter in periampullary carcinomas.

Authors :
Gregório C
Thakur S
Camara Rivero R
Márcia Dos Santos Machado S
Cuenin C
Carreira C
White V
Cree IA
Vukojevic K
Glavina Durdov M
Bersch Osvaldt A
Ashton-Prolla P
Herceg Z
Talukdar FR
Source :
Gene [Gene] 2023 Jul 15; Vol. 873, pp. 147460. Date of Electronic Publication: 2023 May 05.
Publication Year :
2023

Abstract

Genetic and epigenetic alterations of the telomere maintenance machinery like telomere length and telomerase reverse transcriptase (encoded by TERT gene) are reported in several human malignancies. However, there is limited knowledge on the status of the telomere machinery in periampullary carcinomas (PAC) which are rare and heterogeneous groups of cancers arising from different anatomic sites around the ampulla of Vater. In the current study, we investigated the relative telomere length (RTL) and the most frequent genetic and epigenetic alterations in the TERT promoter in PAC and compared it with tumor-adjacent nonpathological duodenum (NDu). We found shorter RTLs (1.27 vs 1.33, P = 0.01) and lower TERT protein expression (p = 0.04) in PAC tissues as compared to the NDu. Although we did not find any mutation at two reactivating hotspot mutation sites of the TERT promoter, we detected polymorphism in 45% (9/20) of the cases at rs2853669 (T > C). Also, we found a hypermethylated region in the TERT promoter of PACs consisting of four CpGs (cg10896616 with Δβ 7%; cg02545192 with Δβ 9%; cg03323598 with Δβ 19%; and cg07285213 with Δβ 15%). In conclusion, we identified shorter telomeres with DNA hypermethylation in the TERT promoter region and lower TERT protein expression in PAC tissues. These results could be used further to investigate molecular pathology and develop theranostics for PAC.<br />Competing Interests: Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.<br /> (Copyright © 2023. Published by Elsevier B.V.)

Details

Language :
English
ISSN :
1879-0038
Volume :
873
Database :
MEDLINE
Journal :
Gene
Publication Type :
Academic Journal
Accession number :
37150235
Full Text :
https://doi.org/10.1016/j.gene.2023.147460