The Nrf1 and Nrf2 Balance in Oxidative Stress Regulation and Androgen Signaling in Prostate Cancer Cells

Cancers

Michelle A. Schultz²  Asim B. Abdel-Mageed¹ 

[1] Department of Urology, Tulane University Medical Center, 1430 Tulane Avenue, New Orleans, LA 70112, USA; E-Mail:;Department of Pharmacology, Tulane University Medical Center, 1430 Tulane Avenue, New Orleans, LA 70112, USA; E-Mail:

关键词: Nrf1 (NF-E2 related factor-1);    Nrf2 (NF-E2 related factor-2);    prostate cancer;    oxidative stress;    androgen independence;    androgen deprivation therapy;    reactive oxygen species (ROS);    androgen receptor (AR);    di-hydrotestosterone (DHT);   

DOI  :  10.3390/cancers2021354

来源: mdpi

【 摘 要 】

Reactive oxygen species (ROS) signaling has recently sparked a surge of interest as being the molecular underpinning for cancer cell survival, but the precise mechanisms involved have not been completely elucidated. This review covers the possible roles of two ROS-induced transcription factors, Nrf1 and Nrf2, and the antioxidant proteins peroxiredoxin-1 (Prx-1) and Thioredoxin-1 (Txn-1) in modulating AR expression and signaling in aggressive prostate cancer (PCa) cells. In androgen independent (AI) C4-2B cells, in comparison to the parental androgen dependent (AD) LNCaP cells, we present evidence of high Nrf1 and Prx-1 expression and low Nrf2 expression in these aggressive PCa cells. Furthermore, in DHT treated C4-2B cells, increased expression of the p65 (active) isoform of Nrf1 correlated with enhanced AR transactivation. Our findings implicate a crucial balance of Nrf1 and Nrf2 signaling in regulating AR activity in AI-PCa cells. Here we will discuss how understanding the mechanisms by which oxidative stress may affect AR signaling may aid in developing novel therapies for AI-PCa.

【 授权许可】

CC BY   
© 2010 by the authors; licensee MDPI, Basel, Switzerland.