Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2017 Oct:118:42-53.
doi: 10.1016/j.critrevonc.2017.08.009. Epub 2017 Aug 30.

Targeting androgen-independent pathways: new chances for patients with prostate cancer?

Affiliations
Review

Targeting androgen-independent pathways: new chances for patients with prostate cancer?

C Cattrini et al. Crit Rev Oncol Hematol. 2017 Oct.

Abstract

Androgen deprivation therapy (ADT) is the mainstay treatment for advanced prostate cancer (PC). Most patients eventually progress to a condition known as castration-resistant prostate cancer (CRPC), characterized by lack of response to ADT. Although new androgen receptor signaling (ARS) inhibitors and chemotherapeutic agents have been introduced to overcome resistance to ADT, many patients progress because of primary or acquired resistance to these agents. This comprehensive review aims at exploring the mechanisms of resistance and progression of PC, with specific focus on alterations which lead to the activation of androgen receptor (AR)-independent pathways of survival. Our work integrates available clinical and preclinical data on agents which target these pathways, assessing their potential clinical implication in specific settings of patients. Given the rising interest of the scientific community in cancer immunotherapy strategies, further attention is dedicated to the role of immune evasion in PC.

Keywords: Androgen receptor; Castration-resistant prostate cancer; Phenotypic plasticity; Stress response; Survival pathways; Tumor heterogeneity.

PubMed Disclaimer

MeSH terms