Melanoma redox biology and the emergence of drug resistance.

Adv Cancer Res

Mātai Hāora-Centre for Redox Biology and Medicine, Department of Pathology and Biomedical Science, University of Otago, Christchurch, New Zealand. Electronic address:

Published: July 2024

AI Article Synopsis

  • * Patients often face initial therapy unresponsiveness or develop resistance, highlighting the need for new strategies that can kill resistant melanoma cells or prevent their development.
  • * The text reviews the role of oxidative stress in melanoma, suggesting that targeting antioxidant pathways might be key to limiting the emergence of drug-resistant cells.

Article Abstract

Melanoma is the deadliest form of skin cancer, with the loss of approximately 60,000 lives world-wide each year. Despite the development of targeted therapeutics, including compounds that have selectivity for mutant oncoproteins expressed only in cancer cells, many patients are either unresponsive to initial therapy or their tumors acquire resistance. This results in five-year survival rates of below 25%. New strategies that either kill drug-resistant melanoma cells or prevent their emergence would be extremely valuable. Melanoma, like other cancers, has long been described as being under increased oxidative stress, resulting in an increased reliance on antioxidant defense systems. Changes in redox homeostasis are most apparent during metastasis and during the metabolic reprogramming associated with the development of treatment resistance. This review discusses oxidative stress in melanoma, with a particular focus on targeting antioxidant pathways to limit the emergence of drug resistant cells.

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Source
http://dx.doi.org/10.1016/bs.acr.2024.06.004DOI Listing

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