Is Autophagy Inhibition in Combination with Temozolomide a Therapeutically Viable Strategy?

Cells

Department of Pharmacology and Toxicology, Massey Cancer Center, Virginia Commonwealth University, 401 College St., Richmond, VA 23298, USA.

Published: February 2023

AI Article Synopsis

  • Temozolomide is an oral chemotherapy drug primarily used to treat glioblastoma multiforme and has shown effectiveness in recurrent anaplastic astrocytoma and metastatic melanoma.
  • Resistance to temozolomide significantly limits its effectiveness, particularly in glioblastoma patients, with proposed mechanisms including the development of cytoprotective autophagy.
  • This review discusses the evidence surrounding autophagy as a survival mechanism in tumor cells and suggests that targeting autophagy could enhance the effectiveness of temozolomide and help overcome resistance.

Article Abstract

Temozolomide is an oral alkylating agent that is used as the first line treatment for glioblastoma multiform, and in recurrent anaplastic astrocytoma, as well as having demonstrable activity in patients with metastatic melanoma. However, as the case with other chemotherapeutic agents, the development of resistance often limits the therapeutic benefit of temozolomide, particularly in the case of glioblastoma. A number of resistance mechanisms have been proposed including the development of cytoprotective autophagy. Cytoprotective autophagy is a survival mechanism that confers upon tumor cells the ability to survive in a nutrient deficient environment as well as under external stresses, such as cancer chemotherapeutic drugs and radiation, in part through the suppression of apoptotic cell death. In this review/commentary, we explore the available literature and provide an overview of the evidence for the promotion of protective autophagy in response to temozolomide, highlighting the possibility of targeting autophagy as an adjuvant therapy to potentially increase the effectiveness of temozolomide and to overcome the development of resistance.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9954434PMC
http://dx.doi.org/10.3390/cells12040535DOI Listing

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