Riboceine and N-acetylcysteine protect normal prostate cells from chemotherapy-induced oxidative stress while selectively modulating the cytotoxicity of methotrexate and docetaxel in prostate (PC-3) and breast cancer (MCF-7) cells
RIB and NAC provide selective cytoprotection to normal prostate cells during chemotherapy while maintaining anticancer effects in sensitive prostate cancer cells. However, their concurrent use in resistant cancers like MCF-7 may reduce drug efficacy, warranting cautious clinical application. Time-shifted antioxidant administration (e.g., post-chemotherapy) could be explored as a strategy to balance protection and efficacy. Future studies should include in vivo validation, apoptosis profiling, and protein-level mechanistic assays to confirm the predicted pathways.
Authors
- Eunice Dotse (ORCID: https://orcid.org/0000-0002-1118-6942)
- Joseph Kofi Abankwah (ORCID: https://orcid.org/0009-0003-9749-5467)
- Regina Appiah‐Opong (ORCID: https://orcid.org/0000-0003-4219-7107)
- Trudy Janice Philips (ORCID: https://orcid.org/0000-0003-3279-6333)
- Benoit Banga N’guessan (ORCID: https://orcid.org/0000-0002-0749-2218)
Institutions
- University of Ghana (GH)
- University of Health and Allied Sciences (GH)
- Noguchi Memorial Institute for Medical Research (GH)
Publication Details
- Journal
- Biomedicine & Pharmacotherapy
- Published
- 2025-07-20
- DOI
- https://doi.org/10.1016/j.biopha.2025.118355
- Citations
- 1
- Primary Topic
- Cancer, Hypoxia, and Metabolism
- Type
- article
- Field-Weighted Citation Impact
- 0.94