Targeting mRNA-coding genes in prostate cancer using CRISPR/Cas9 technology with a special focus on androgen receptor

Mobina Tabibian1, Fahimeh Salasar Moghaddam2, Elahe Motevaseli3

  • 1Department of Cellular and Molecular Biology, Faculty of Life Sciences and Biotechnologies, Shahid Beheshti University, Tehran, Iran.

Abstract

Insights

CRISPR/Cas9 technology shows promise for prostate cancer treatment by modifying key genes, including those in androgen receptor signaling. This gene-editing tool has demonstrated effectiveness in reducing tumor burden in preclinical models.

Area of Science:

  • Oncology
  • Genetics
  • Molecular Biology

Background:

  • Prostate cancer is a prevalent malignancy in men.
  • Gene signaling pathways are critical in prostate cancer progression.
  • CRISPR/Cas9 gene editing offers a novel therapeutic strategy.

Purpose of the Study:

  • To review recent advancements in CRISPR/Cas9 applications for prostate cancer.
  • To focus on the modification of androgen receptor signaling pathways.
  • To highlight CRISPR/Cas9's role in altering prostate cancer phenotypes.

Main Methods:

  • CRISPR/Cas9 gene editing was employed to modify gene expression in prostate cancer cells.
  • Targeted genes were analyzed for their role in prostate cancer phenotypes.
  • Efficacy was assessed in preclinical animal models of prostate cancer.

Main Results:

  • CRISPR/Cas9 successfully targeted multiple genes in prostate cancer cells.
  • Modulation of androgen receptor signaling genes impacted castration-resistant prostate cancer growth.
  • PI3K/AKT/mTOR and immune response genes were also modulated effectively.

Conclusions:

  • CRISPR/Cas9 technology has proven effective in targeting critical genes in prostate cancer.
  • Preclinical studies show potential for reducing tumor burden.
  • Future clinical applications of CRISPR/Cas9 may significantly alter prostate cancer outcomes.