Unmasking Neuroendocrine Prostate Cancer with a Machine Learning-Driven Seven-Gene Stemness Signature That Predicts Progression

Prostate cancer (PCa) poses a significant global health challenge, particularly due to its progression into aggressive forms like neuroendocrine prostate cancer (NEPC). This study developed and validated a stemness-associated gene signature using advanced machine learning techniques, including Rando...

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Veröffentlicht in:International journal of molecular sciences 2024-11, Vol.25 (21), p.11356
Hauptverfasser: Sabater, Agustina, Sanchis, Pablo, Seniuk, Rocio, Pascual, Gaston, Anselmino, Nicolas, Alonso, Daniel F, Cayol, Federico, Vazquez, Elba, Marti, Marcelo, Cotignola, Javier, Toro, Ayelen, Labanca, Estefania, Bizzotto, Juan, Gueron, Geraldine
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Sprache:eng
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Zusammenfassung:Prostate cancer (PCa) poses a significant global health challenge, particularly due to its progression into aggressive forms like neuroendocrine prostate cancer (NEPC). This study developed and validated a stemness-associated gene signature using advanced machine learning techniques, including Random Forest and Lasso regression, applied to large-scale transcriptomic datasets. The resulting seven-gene signature ( , , , , , , and ) was validated across independent cohorts and patient-derived xenograft (PDX) models. This signature demonstrated strong prognostic value for progression-free, disease-free, relapse-free, metastasis-free, and overall survival. Importantly, the signature not only identified specific NEPC subtypes, such as large-cell neuroendocrine carcinoma, which is associated with very poor outcomes, but also predicted a poor prognosis for PCa cases that exhibit this molecular signature, even when they were not histopathologically classified as NEPC. This dual prognostic and classifier capability makes the seven-gene signature a robust tool for personalized medicine, providing a valuable resource for predicting disease progression and guiding treatment strategies in PCa management.
ISSN:1422-0067
1661-6596
1422-0067
DOI:10.3390/ijms252111356