4.8 Article

Tumor subtype defines distinct pathways of molecular and clinical progression in primary prostate cancer

Journal

JOURNAL OF CLINICAL INVESTIGATION
Volume 131, Issue 10, Pages -

Publisher

AMER SOC CLINICAL INVESTIGATION INC
DOI: 10.1172/JCI147878

Keywords

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Funding

  1. Prostate Cancer Foundation
  2. NCI [P50CA211024, R01CA233650]
  3. Urology Care Foundation Rising Star in Urology Research Award
  4. Damon Runyon Cancer Research Foundation MetLife Foundation Family Clinical Investigator Award
  5. US Department of Defense Postdoctoral Fellowship [W81XWH-17-1-013 7]
  6. Foundation AIRC [IG 19221]

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The study reveals that different subtypes of prostate cancer follow distinct pathways of progression, with late events associated with prognosis. Late events show strikingly different features at radical prostatectomy, suggesting that common clinical parameters may be influenced by underlying tumor lineage and impact treatment decisions.
BACKGROUND. Molecular characterization of prostate cancer (PCa) has revealed distinct subclasses based on underlying genomic alterations occurring early in the natural history of the disease. However, how these early alterations influence subsequent molecular events and the course of the disease over its long natural history remains unclear. METHODS. We explored the molecular and clinical progression of different genomic subtypes of PCa using distinct tumor lineage models based on human genomic and transcriptomic data. We developed transcriptional classifiers, and defined early and late categories of molecular subclasses from 8,158 PCa patients. Molecular subclasses were correlated with clinical outcomes and pathologic characteristics using Kaplan-Meier and logistic regression analyses. RESULTS. We identified PTEN and CHD1 alterations as subtype-specific late progression events specifically in ERGoverexpressing (ERG+) and SPOP-mutant tumors, respectively, and 2 distinct progression models consisting of ERG/PTEN (normal to ERG+ to PTEN-deleted) and SPOP/CHD1 (normal to SPOP-mutated to CHD1-deleted) with shared early tumorigenesis but distinct pathways toward progression. We found that within ERG+ and SPOP-mutant subtypes, late events were associated with worse prognosis. Importantly, the clinical and pathologic features associated with distinct late events at radical prostatectomy were strikingly different; PTEN deletions were associated with increased locoregional stage, while CHD1 deletions were only associated with increased grade, despite equivalent metastatic potential. CONCLUSION. These findings suggest a paradigm in which specific subtypes of PCa follow distinct pathways of progression, at both the molecular and clinical levels. Therefore, the interpretation of common clinical parameters such as locoregional tumor stage may be influenced by the underlying tumor lineage, and potentially influence management decisions.

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