2024RESEARCH INVENTION JOURNAL OF BIOLOGICAL AND APPLIED SCIENCESOpen access

Targeting Androgen Receptor Variants in Castration-Resistant Prostate Cancer (CRPC)

Omeye Francis I.

Open full text 1 citations

Abstract

Castration-resistant prostate cancer (CRPC) remains a lethal stage of prostate cancer, characterized by resistance to androgen deprivation therapy (ADT) and poor clinical prognosis. One of the key drivers in CRPC progression is the androgen receptor (AR), specifically the emergence of androgen receptor variants (AR-Vs) that sustain AR signaling even in the absence of androgens. AR-Vs, such as AR-V7, promote androgen-independent activation of oncogenic pathways, leading to uncontrolled cell proliferation and therapeutic resistance. Targeting AR-Vs offers a promising therapeutic strategy to manage CRPC effectively. This review explores the molecular mechanisms underpinning AR-V expression, examines the roles of major AR variants in CRPC progression, and evaluates current and emerging therapies targeting AR-Vs. By summarizing recent advancements and the limitations of current approaches, we highlight potential future directions to improve therapeutic outcomes for CRPC patients. Keywords: Androgen receptor variants, Castration-resistant prostate cancer, AR-V7, Androgen deprivation therapy, Targeted therapy, Oncogenic pathways

Open-access reader

About this research paper

What this paper is about

Castration-resistant prostate cancer (CRPC) remains a lethal stage of prostate cancer, characterized by resistance to androgen deprivation therapy (ADT) and poor clinical prognosis. One of the key drivers in CRPC progression is the androgen receptor (AR), specifically the emergence of androgen receptor variants (AR-Vs) that sustain AR signaling even in the absence of androgens. AR-Vs, such as AR-V7, promote androgen-independent activation of oncogenic pathways, leading to uncontrolled cell proliferation and therapeutic resistance. Targeting AR-Vs offers a promising therapeutic strategy to manage CRPC effectively. This review explores the molecular mechanisms underpinning AR-V expression, examines the roles of major AR variants in CRPC progression, and evaluates current and emerging therapies targeting AR-Vs. By summarizing recent advancements and the limitations of current approaches, we highlight potential future directions to improve therapeutic outcomes for CRPC patients. Keywords: Androgen receptor variants, Castration-resistant prostate cancer, AR-V7, Androgen deprivation therapy, Targeted therapy, Oncogenic pathways

Why it matters

OpenAlex reports 1 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Castration-resistant prostate cancer (CRPC) remains a lethal stage of prostate cancer, characterized by resistance to androgen deprivation therapy (ADT) and poor clinical prognosis. One of the key drivers in CRPC progression is the androgen receptor (AR), specifically the emergence of androgen receptor variants (AR-Vs) that sustain AR signaling even in the absence of androgens. AR-Vs, such as AR-V7, promote androgen-independent activation of oncogenic pathways, leading to uncontrolled cell proliferation and therapeutic resistance. Targeting AR-Vs offers a promising therapeutic strategy to manage CRPC effectively. This review explores the molecular mechanisms underpinning AR-V expression, examines the roles of major AR variants in CRPC progression, and evaluates current and emerging therapies targeting AR-Vs. By summarizing recent advancements and the limitations of current approaches, we highlight potential future directions to improve therapeutic outcomes for CRPC patients. Keywords: Androgen receptor variants, Castration-resistant prostate cancer, AR-V7, Androgen deprivation therapy, Targeted therapy, Oncogenic pathways

Key concepts: Androgen receptor, Prostate cancer, Androgen deprivation therapy, Androgen, Enzalutamide, Cancer research, Medicine, Oncology

Related papers

Back to paper searchBrowse research topicsOriginal source
Targeting Androgen Receptor Variants in Castration-Resistant Prostate Cancer (CRPC) — Research Paper | ScholarLens