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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.
Abstract:
Drug repurposing can overcome both substantial costs and the lengthy process of new drug discovery and development in cancer treatment. Some Food and Drug Administration (FDA)-approved drugs have been found to have the potential to be repurposed as anti-cancer drugs. However, the progress is slow due to only a handful of strategies employed to identify drugs with repurposing potential. In this study, we evaluated GPCR-targeting drugs by high throughput screening (HTS) for their repurposing potential in triple-negative breast cancer (TNBC) and drug-resistant human epidermal growth factor receptor-2-positive (HER2+) breast cancer (BC), due to the dire need to discover novel targets and drugs in these subtypes. We assessed the efficacy and potency of drugs/compounds targeting different GPCRs for the growth rate inhibition in the following models: two TNBC cell lines (MDA-MB-231 and MDA-MB-468) and two HER2+ BC cell lines (BT474 and SKBR3), sensitive or resistant to lapatinib + trastuzumab, an effective combination of HER2-targeting therapies. We identified six drugs/compounds as potential hits, of which 4 were FDA-approved drugs. We focused on β-adrenergic receptor-targeting nebivolol as a candidate, primarily because of the potential role of these receptors in BC and its excellent long-term safety profile. The effects of nebivolol were validated in an independent assay in all the cell line models. The effects of nebivolol were independent of its activation of β3 receptors and nitric oxide production. Nebivolol reduced invasion and migration potentials which also suggests its inhibitory role in metastasis. Analysis of the Surveillance, Epidemiology and End Results (SEER)-Medicare dataset found numerically but not statistically significant reduced risk of all-cause mortality in the nebivolol group. In-depth future analyses, including detailed in vivo studies and real-world data analysis with more patients, are needed to further investigate the potential of nebivolol as a repurposed therapy for BC.
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.
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