4.7 Review

Modulation of redox homeostasis: A strategy to overcome cancer drug resistance

Journal

FRONTIERS IN PHARMACOLOGY
Volume 14, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphar.2023.1156538

Keywords

redox homeostasis; drug resistance; cancer therapy; reactive oxygen species; redox signaling

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Cancer treatment is hindered by resistance to conventional therapeutic strategies, and redox homeostasis manipulation can effectively overcome drug resistance. Reactive oxygen species (ROS) regulate multiple signaling pathways and cancer cells upregulate their antioxidant system to cope with elevated ROS levels during therapy, resulting in therapeutic resistance. This review highlights the interplay between redox modification, signaling pathways, and therapeutic resistance, including altered drug efflux, action targets and metabolism, enhanced DNA damage repair, maintained stemness, and reshaped tumor microenvironment. A comprehensive understanding of these interrelationships can improve treatment efficacy.
Cancer treatment is hampered by resistance to conventional therapeutic strategies, including chemotherapy, immunotherapy, and targeted therapy. Redox homeostasis manipulation is one of the most effective innovative treatment techniques for overcoming drug resistance. Reactive oxygen species (ROS), previously considered intracellular byproducts of aerobic metabolism, are now known to regulate multiple signaling pathways as second messengers. Cancer cells cope with elevated amounts of ROS during therapy by upregulating the antioxidant system, enabling tumor therapeutic resistance via a variety of mechanisms. In this review, we aim to shed light on redox modification and signaling pathways that may contribute to therapeutic resistance. We summarized the molecular mechanisms by which redox signaling-regulated drug resistance, including altered drug efflux, action targets and metabolism, enhanced DNA damage repair, maintained stemness, and reshaped tumor microenvironment. A comprehensive understanding of these interrelationships should improve treatment efficacy from a fundamental and clinical research point of view.

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