Emerging proteins involved in castration‑resistant prostate cancer via the AR‑dependent and AR‑independent pathways (Review)

Int J Oncol. 2023 Nov;63(5):127. doi: 10.3892/ijo.2023.5575. Epub 2023 Sep 21.

Abstract

Despite achieving optimal initial responses to androgen deprivation therapy, most patients with prostate cancer eventually progress to a poor prognosis state known as castration‑resistant prostate cancer (CRPC). Currently, there is a notable absence of reliable early warning biomarkers and effective treatment strategies for these patients. Although androgen receptor (AR)‑independent pathways have been discovered and acknowledged in recent years, the AR signaling pathway continues to play a pivotal role in the progression of CRPC. The present review focuses on newly identified proteins within human CRPC tissues. These proteins encompass both those involved in AR‑dependent and AR‑independent pathways. Specifically, the present review provides an in‑depth summary and analysis of the emerging proteins within AR bypass pathways. Furthermore, the significance of these proteins as potential biomarkers and therapeutic targets for treating CRPC is discussed. Therefore, the present review offers valuable theoretical insights and clinical perspectives to comprehensively enhance the understanding of CRPC.

Keywords: androgen receptor; biomarker; castration‑resistant prostate cancer; protein; signaling pathway; therapeutic target.

Publication types

  • Review

MeSH terms

  • Androgen Antagonists
  • Humans
  • Male
  • Prostatic Neoplasms, Castration-Resistant* / genetics
  • Receptors, Androgen*

Substances

  • Receptors, Androgen
  • Androgen Antagonists

Grants and funding

The present study was supported by grants from The National Natural Science Foundation of China Youth Science Foundation Project (grant no. 81802571), Zhejiang Medical and Health Science and Technology Project (grant no. 2019RC039) and Keqiao District Scientific Research Project (grant no. 2021KZ42).