Context-dependent effects of CDKN2A and other 9p21 gene losses during the evolution of oesophageal cancer

Piyali Ganguli, Celia C. Basanta, Akram Mendez, Maria Armero, Aeman Zahra, Amelia A. Sagrado,Hrvoje Misetic,Ginny Devonshire,Gavin Kelly,Adam Freeman,Mary Green,Emma Nye, Oesophageal Cancer Clinical and Molecular Stratification (OCCAMS) Consortium,Manuel Rodriguez-Justo,Jo Spencer,Rebecca C. Fitzgerald,Francesca D. Ciccarelli

biorxiv(2024)

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摘要
CDKN2A is a tumour suppressor gene located in chromosome 9p21 and frequently lost in Barrett’s oesophagus (BO) and oesophageal adenocarcinoma (OAC). How CDKN2A and other 9p21 gene co-deletions affect OAC evolution remains understudied. We explored the effects of 9p21 loss in OACs and cancer progressor and non-progressor BOs with matched genomic, transcriptomic, and clinical data. Despite its cancer driver role, CDKN2A loss in BO prevents OAC initiation by counter-selecting acquisition of TP53 alterations. 9p21 gene co-deletions predict poor patient survival in OAC but not BO through context-dependent effects on cell cycle, oxidative phosphorylation, and interferon response. Immune quantifications using bulk transcriptome, RNAscope and high-dimensional tissue imaging showed that IFNE loss reduces immune infiltration in BO but not OAC. Mechanistically, CDKN2A loss suppresses the maintenance of squamous epithelium, contributing to a more aggressive phenotype. Our study demonstrates context-dependent roles of cancer genes during disease evolution, with consequences for cancer detection and patient management. ### Competing Interest Statement The authors have declared no competing interest.
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