Prostate cancer progression modeling provides insight into dynamic molecular changes associated with progressive disease states.


Journal

Cancer research communications
ISSN: 2767-9764
Titre abrégé: Cancer Res Commun
Pays: United States
ID NLM: 9918281580506676

Informations de publication

Date de publication:
30 Sep 2024
Historique:
accepted: 25 09 2024
received: 06 04 2024
revised: 27 08 2024
medline: 30 9 2024
pubmed: 30 9 2024
entrez: 30 9 2024
Statut: aheadofprint

Résumé

Prostate cancer is a significant health concern and the most commonly diagnosed cancer in men worldwide. Understanding the complex process of prostate tumor evolution and progression is crucial for improved diagnosis, treatments, and patient outcomes. Previous studies have focused on unraveling the dynamics of prostate cancer evolution using phylogenetic or lineage analysis approaches. However, those approaches have limitations in capturing the complete disease process or incorporating genomic and transcriptomic variations comprehensively. In this study, we applied a novel computational approach to derive a prostate cancer progression model using multi-dimensional data from 497 prostate tumor samples and 52 tumor-adjacent normal samples obtained from the TCGA study. The model was validated using data from an independent cohort of 545 primary tumor samples. By integrating transcriptomic and genomic data, our model provides a comprehensive view of prostate tumor progression, identifies crucial signaling pathways and genetic events, and uncovers distinct transcription signatures associated with disease progression. Our findings have significant implications for cancer research and hold promise for guiding personalized treatment strategies in prostate cancer.

Identifiants

pubmed: 39347576
pii: 748713
doi: 10.1158/2767-9764.CRC-24-0210
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Runpu Chen (R)

University at Buffalo, Buffalo, NY, United States.

Li Tang (L)

Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.

Thomas Melendy (T)

Jacobs School of Medicine & Biomedical Sciences, Buffalo, NY, United States.

Le Yang (L)

University at Buffalo, Buffalo, NY, United States.

Steve Goodison (S)

Mayo Clinic, Jacksonville, FL, United States.

Yijun Sun (Y)

University at Buffalo, Buffalo, NY, United States.

Classifications MeSH