AI Article Synopsis

  • Advances in cancer treatment face significant challenges due to treatment resistance, with autophagy playing a key role in this issue.
  • Studies indicate that autophagy contributes to resistance across various cancer types, particularly in relation to chemotherapies and targeted therapies, linked to signaling pathways like MAPK and PI3K/AKT.
  • This text reviews current evidence on how autophagy interacts with these pathways and highlights new molecular mechanisms, focusing on the interactions of p62/KEAP1/NRF2 and FOXO3A/PUMA in contributing to chemoresistance.

Article Abstract

Despite advances in diagnostic tools and therapeutic options, treatment resistance remains a challenge for many cancer patients. Recent studies have found evidence that autophagy, a cellular pathway that delivers cytoplasmic components to lysosomes for degradation and recycling, contributes to treatment resistance in different cancer types. A role for autophagy in resistance to chemotherapies and targeted therapies has been described based largely on associations with various signaling pathways, including MAPK and PI3K/AKT signaling. However, our current understanding of the molecular mechanisms underlying the role of autophagy in facilitating treatment resistance remains limited. Here we provide a comprehensive summary of the evidence linking autophagy to major signaling pathways in the context of treatment resistance and tumor progression, and then highlight recently emerged molecular mechanisms underlying autophagy and the p62/KEAP1/NRF2 and FOXO3A/PUMA axes in chemoresistance.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6896088PMC
http://dx.doi.org/10.3390/cancers11111775DOI Listing

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