Non-coding RNAs in BRAF-mutant melanoma: targets, indicators, and therapeutic potential.
Autor: | Afsar S; Department of Virology, Sri Venkateswara University, Tirupathi, Andhra Pradesh, 517502, India. mammoth.afsar1@gmail.com., Syed RU; Department of Pharmaceutics, College of Pharmacy, University of Ha'il, 81442, Hail, Saudi Arabia. ru.syed@outlook.com., Khojali WMA; Department of Pharmaceutical Chemistry, College of Pharmacy, University of Hail, 81442, Hail, Saudi Arabia.; Department of Pharmaceutical Chemistry, Faculty of Pharmacy, Omdurman Islamic University, Omdurman, 14415, Sudan., Masood N; Chemistry Department, Faculty of Science, University of Ha'il, P.O. Box 2440, 81451, Ha'il,, Saudi Arabia., Osman ME; Department of Clinical Pharmacy, Faculty of Pharmacy, University of Hail, Hail, Saudi Arabia., Jyothi JS; Department of Pharmaceutics, Hindu College of Pharmacy, Andhra Pradesh, India., Hadi MA; Department of Pharmaceutics, Bhaskar Pharmacy College, Moinabad, R.R.District, Hyderabad, 500075, Telangana, India., Khalifa AAS; Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, University of Hail, 81442, Hail, Saudi Arabia., Aboshouk NAM; Department of Clinical Laboratory Sciences, College of Applied Medical Sciences, University of Hail, 81442, Hail, Saudi Arabia., Alsaikhan HA; College of Pharmacy, University of Ha'il, 81442, Hail, Saudi Arabia., Alafnan AS; College of Pharmacy, University of Ha'il, 81442, Hail, Saudi Arabia., Alrashidi BA; College of Pharmacy, University of Ha'il, 81442, Hail, Saudi Arabia. |
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Jazyk: | angličtina |
Zdroj: | Naunyn-Schmiedeberg's archives of pharmacology [Naunyn Schmiedebergs Arch Pharmacol] 2024 Aug 21. Date of Electronic Publication: 2024 Aug 21. |
DOI: | 10.1007/s00210-024-03366-3 |
Abstrakt: | Melanoma, a highly aggressive skin cancer, is often driven by BRAF mutations, such as the V600E mutation, which promotes cancer growth through the MAPK pathway and contributes to treatment resistance. Understanding the role of non-coding RNAs (ncRNAs) in these processes is crucial for developing new therapeutic strategies. This review aims to elucidate the relationship between ncRNAs and BRAF mutations in melanoma, focusing on their regulatory roles and impact on treatment resistance. We comprehensively reviewed current literature to synthesize evidence on ncRNA-mediated regulation of BRAF-mutant melanoma and their influence on therapeutic responses. Key ncRNAs, including microRNAs and long ncRNAs, were identified as significant regulators of melanoma development and therapy resistance. MicroRNAs such as miR-15/16 and miR-200 families modulate critical pathways like Wnt signaling and melanogenesis. Long ncRNAs like ANRIL and SAMMSON play roles in cell growth, invasion, and drug susceptibility. Specific ncRNAs, such as BANCR and RMEL3, intersect with the MAPK pathway, highlighting their potential as therapeutic targets or biomarkers in BRAF-mutant melanoma. Additionally, ncRNAs involved in drug resistance, such as miR-579-3p and miR-1246, target processes like autophagy and immune checkpoint regulation. This review highlights the pivotal roles of ncRNAs in regulating BRAF-mutant melanoma and their contribution to drug resistance. These findings underscore the potential of ncRNAs as biomarkers and therapeutic targets, paving the way for innovative treatments to improve outcomes for melanoma patients. (© 2024. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.) |
Databáze: | MEDLINE |
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