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Prostate cancer progression modeling provides insight into dynamic molecular changes associated with progressive disease states.
Chen, Runpu; Tang, Li; Melendy, Thomas; Yang, Le; Goodison, Steve; Sun, Yijun.
Afiliación
  • Chen R; University at Buffalo, Buffalo, NY, United States.
  • Tang L; Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States.
  • Melendy T; Jacobs School of Medicine & Biomedical Sciences, Buffalo, NY, United States.
  • Yang L; University at Buffalo, Buffalo, NY, United States.
  • Goodison S; Mayo Clinic, Jacksonville, FL, United States.
  • Sun Y; University at Buffalo, Buffalo, NY, United States.
Cancer Res Commun ; 2024 Sep 30.
Article en En | MEDLINE | ID: mdl-39347576
ABSTRACT
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.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancer Res Commun Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Cancer Res Commun Año: 2024 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos