Screening of GPCR drugs for repurposing in breast cancer

Noor Mazin Abdulkareem1, Raksha Bhat2, Reid T Powell3

  • 1Department of Pharmacological and Pharmaceutical Sciences, University of Houston College of Pharmacy, Houston, TX, United states.

Frontiers in Pharmacology
|December 23, 2022
PubMed

Insights

Drug repurposing offers a faster path to cancer treatments. Researchers screened GPCR-targeting drugs, identifying nebivolol as a potential therapy for triple-negative and HER2-positive breast cancer, showing promise in inhibiting metastasis.

Area of Science:

  • Oncology
  • Pharmacology
  • Drug Discovery

Background:

  • Drug repurposing accelerates cancer treatment development by utilizing existing FDA-approved medications.
  • Identifying novel therapeutic strategies for triple-negative breast cancer (TNBC) and drug-resistant HER2-positive breast cancer (BC) remains critical.
  • Current drug repurposing efforts for cancer are limited by a scarcity of effective identification strategies.

Purpose of the Study:

  • To evaluate G protein-coupled receptor (GPCR)-targeting drugs for repurposing potential against TNBC and HER2+ BC.
  • To assess the efficacy of GPCR-targeting agents in inhibiting cancer cell growth in relevant preclinical models.
  • To identify promising drug candidates for further investigation in challenging breast cancer subtypes.

Main Methods:

  • High-throughput screening (HTS) of GPCR-targeting drugs against two TNBC and two HER2+ BC cell lines.
  • Assessment of drug efficacy and potency in inhibiting cancer cell growth rate.
  • Validation of lead compounds in independent assays and analysis of their effects on cell invasion and migration.
  • Retrospective analysis of the SEER-Medicare dataset to evaluate all-cause mortality risk.

Main Results:

  • Six drug candidates, including four FDA-approved drugs, were identified as potential hits.
  • Nebivolol, a β-adrenergic receptor-targeting drug, demonstrated validated anti-cancer effects across all tested cell lines.
  • Nebivolol inhibited cancer cell invasion and migration, suggesting potential anti-metastatic properties.
  • SEER-Medicare data showed a non-statistically significant trend towards reduced all-cause mortality in nebivolol users.

Conclusions:

  • Nebivolol exhibits potential as a repurposed therapeutic agent for specific breast cancer subtypes.
  • Further in-depth in vivo studies and larger real-world data analyses are warranted to confirm nebivolol's efficacy and safety for breast cancer treatment.
  • The study highlights the value of GPCR-targeting drug screening for identifying novel cancer therapies.