KDM4A promotes NEPC progression through regulation of MYC expression

Neuroendocrine prostate cancer (NEPC) is a highly aggressive and lethal subtype of prostate cancer (PCa) that often emerges in response to androgen receptor pathway inhibitors (ARPIs), which are widely used in treating metastatic castration-resistant and hormone-sensitive prostate cancer. The incidence of NEPC is increasing, yet effective therapeutic strategies remain limited due to an incomplete understanding of its molecular drivers. Through transcriptomic analyses of human prostate tumor samples, we identified the histone lysine demethylase KDM4A as uniquely overexpressed in human and mouse NEPC compared to prostate adenocarcinoma. Functional validation demonstrated that KDM4A is a key regulator of NEPC progression and a promising therapeutic target, as knockdown or knockout of KDM4A suppresses NEPC cell proliferation in vitro and tumor growth in vivo. Mechanistically, we found that KDM4A directly regulates the transcription of the oncogene MYC, which we show is essential for NEPC cell growth through knockdown and inhibitor studies. Importantly, pharmacologic inhibition of KDM4A using QC6352, a potent pan-KDM4 inhibitor, significantly reduced NEPC cell proliferation in vitro and tumor growth in vivo, providing proof-of-concept for therapeutic targeting. Collectively, our findings establish KDM4A as a critical epigenetic driver of NEPC through MYC regulation and demonstrate its therapeutic potential for this lethal disease that currently lacks effective treatments.

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Publication Details

Journal
Cancer Letters
Published
2025-11-29
DOI
https://doi.org/10.1016/j.canlet.2025.218184
Primary Topic
Prostate Cancer Treatment and Research
Type
article
Field-Weighted Citation Impact
0.00
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article

KDM4A promotes NEPC progression through regulation of MYC expression

Abhinav K. Jain, Barbara A. Foster, Muhammad Amjad Bashir, Peter R. Shepherd et al.
Cancer Letters
Prostate Cancer Treatment and Research
article

KDM4A promotes NEPC progression through regulation of MYC expression

Abhinav K. Jain, Barbara A. Foster, Muhammad Amjad Bashir, Peter R. Shepherd, Min Gyu Lee, Eric Metzger, Christopher J. Logothetis, Feng Wang, Anh Hoang, Sue-Hwa Lin, Xingzhi Song, Jessica Suh, Nora M. Navone, Patricia Troncoso, Ming Zhu, ThucNhi T. Dang, Derek Liang, Michela Mazzocco, Paul Gettys Corn, Ellen Karasik, Daniel E. Frigo, Guocan Wang, Rebecca Schüle, Brandon A. Figueroa, Miao Zhang, Jie Fu, Xin Liang, Chunxia Yan, Fei Yuan, Jiwon Park, Juan L. Contreras, Celia Sze Ling Mak, Bijeta Pradhan, Zhi Tan, Jianhua Zhang, Aiping Luo, Ana Aparicio, Xiaoxuan Wang
article en

Abstract

Neuroendocrine prostate cancer (NEPC) is a highly aggressive and lethal subtype of prostate cancer (PCa) that often emerges in response to androgen receptor pathway inhibitors (ARPIs), which are widely used in treating metastatic castration-resistant and hormone-sensitive prostate cancer. The incidence of NEPC is increasing, yet effective therapeutic strategies remain limited due to an incomplete understanding of its molecular drivers. Through transcriptomic analyses of human prostate tumor samples, we identified the histone lysine demethylase KDM4A as uniquely overexpressed in human and mouse NEPC compared to prostate adenocarcinoma. Functional validation demonstrated that KDM4A is a key regulator of NEPC progression and a promising therapeutic target, as knockdown or knockout of KDM4A suppresses NEPC cell proliferation in vitro and tumor growth in vivo. Mechanistically, we found that KDM4A directly regulates the transcription of the oncogene MYC, which we show is essential for NEPC cell growth through knockdown and inhibitor studies. Importantly, pharmacologic inhibition of KDM4A using QC6352, a potent pan-KDM4 inhibitor, significantly reduced NEPC cell proliferation in vitro and tumor growth in vivo, providing proof-of-concept for therapeutic targeting. Collectively, our findings establish KDM4A as a critical epigenetic driver of NEPC through MYC regulation and demonstrate its therapeutic potential for this lethal disease that currently lacks effective treatments.

Cancer LettersVol. 638
Roswell Park Comprehensive Cancer Center (US), The University of Texas MD Anderson Cancer Center (US), University of Freiburg (DE), Baylor College of Medicine (US), Drug Discovery Laboratory (Norway) (NO), Imaging Systems Technology (United States) (US), Spanish Oncology Genitourinary Group (ES)
Openalex Percentile: Top 44%
Prostate Cancer Treatment and Research
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