Genomic and Epigenomic Analysis of Plasma Cell-Free DNA Identifies Stemness Features Associated with Worse Survival in Lethal Prostate Cancer

We analyzed a total of 220 patients with mCRPC, validated the importance of cell-free AR/enhancer alterations as a prognostic biomarker in lethal mCRPC, and showed that the underlying mechanism for lethality involves reprogramming developmental states toward increased stemness. See related commentary by Nawfal et al., p. 7.

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Publication Details

Journal
Clinical Cancer Research
Published
2024-08-23
DOI
https://doi.org/10.1158/1078-0432.ccr-24-1658
Citations
8
Primary Topic
Prostate Cancer Treatment and Research
Type
article
Field-Weighted Citation Impact
3.35

Funders

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article

Genomic and Epigenomic Analysis of Plasma Cell-Free DNA Identifies Stemness Features Associated with Worse Survival in Lethal Prostate Cancer

Sean S. Park, Jacob J. Orme, Ramandeep K. Babbra, Irfan Alahi et al.
8 citations
Clinical Cancer Research
Prostate Cancer Treatment and Research
3.35
article

Genomic and Epigenomic Analysis of Plasma Cell-Free DNA Identifies Stemness Features Associated with Worse Survival in Lethal Prostate Cancer

Sean S. Park, Jacob J. Orme, Ramandeep K. Babbra, Irfan Alahi, Jace Webster, Chad Z. Tang, Alexander D. Sherry, Sydney Caputo, Dzifa Y. Duose, Peter K. Harris, Alexander L. Shiang, Christopher A. Maher, Lilli Greiner, Wenjia Feng, Ryan Mueller, Savar Sinha, Elisa M. Ledet, Faridi Qaium, Ellen Jaeger, Gabris Ni, Aadel A. Chaudhuri, Breanna Yang, Oliver A. Sartor, Ha X. Dang, Russell K. Pachynski, Pradeep S. Chauhan, Fabrice Lucien, Debanjan Saha, Jessica Linford, Steven Alexander, Patrick J. Miller
article en
8 citations

Abstract

We analyzed a total of 220 patients with mCRPC, validated the importance of cell-free AR/enhancer alterations as a prognostic biomarker in lethal mCRPC, and showed that the underlying mechanism for lethality involves reprogramming developmental states toward increased stemness. See related commentary by Nawfal et al., p. 7.

Clinical Cancer ResearchVol. 31(1)
James S. McDonnell Foundation (US), Tulane University (US), Cedars-Sinai Medical Center (US), Mayo Clinic (US), The University of Texas MD Anderson Cancer Center (US), Washington University in St. Louis (US), Ochsner Baptist Medical Center (US), University of Rochester Medical Center (US), Cancer Clinic (US), Mayo Clinic in Arizona (US), Mayo Clinic in Florida (US)
U.S. Department of Defense, V Foundation for Cancer Research, Amgen, Pfizer, AstraZeneca, Sanofi, Cancer Prevention and Research Institute of Texas, Exelixis, National Comprehensive Cancer Network, Advanced Accelerator Applications, Genentech, Pharmacyclics, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 7%
Prostate Cancer Treatment and Research
3.35
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