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Promising therapy for neuroendocrine prostate cancer: current status and future directions.
Fei, Xin; Xue, Jia-Wei; Wu, Ji-Zhongrong; Yang, Chong-Yi; Wang, Ke-Jie; Ma, Qi.
  • Fei X; Health Science Center, Ningbo University, Ningbo, Zhejiang, China.
  • Xue JW; Health Science Center, Ningbo University, Ningbo, Zhejiang, China.
  • Wu JZ; Department of Urology, The First Hospital of Ninghai, Ningbo, China.
  • Yang CY; Health Science Center, Ningbo University, Ningbo, Zhejiang, China.
  • Wang KJ; Department of Urology, Shengzhou People's Hospital, Shaoxing, China.
  • Ma Q; Department of Urology, The First Hospital of Ninghai, 142 Taoyuan Middle Road, Yuelong Street, Ninghai county, Ningbo, Zhejiang 315699, China.
Ther Adv Med Oncol ; 16: 17588359241269676, 2024.
Article en En | MEDLINE | ID: mdl-39131727
ABSTRACT
Neuroendocrine prostate cancer (NEPC) is a highly aggressive variant of castration-resistant prostate cancer. It is characterized by low or no expression of the androgen receptor (AR), activation of AR-independent signaling, and increased neuroendocrine phenotype. Most of NEPC is induced by treatment of androgen deprivation therapy and androgen receptor pathway inhibitors (ARPIs). Currently, the treatment of NEPC follows the treatment strategy for small-cell lung cancer, lacking effective drugs and specific treatment options. This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (zeste homolog 2 inhibitors, lysine-specific demethylase 1 inhibitors), aurora kinase A inhibitors, poly-ADP-ribose polymerase inhibitors, delta-like ligand 3 targeted therapies, a combination of immunotherapies, etc. Other promising targets and future directions are also discussed in this review. These novel targets and therapies may provide new opportunities for the treatment of NEPC.
This review summarizes potential novel targets and therapies for NEPC treatment, including epigenetic regulators (EZH2 inhibitors, LSD-1 inhibitors), AURKA inhibitors, PARP inhibitors, and DLL3 targeted therapies, and combination of immunotherapies, etc. These novel targets and therapies may provide new opportunities in the treatment of NEPC.
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