Molecular Mechanisms Underlying Autophagy-Mediated Treatment Resistance in Cancer

التفاصيل البيبلوغرافية
العنوان: Molecular Mechanisms Underlying Autophagy-Mediated Treatment Resistance in Cancer
المؤلفون: Cally J Ho, Sharon M. Gorski
المصدر: Cancers, Vol 11, Iss 11, p 1775 (2019)
Cancers
بيانات النشر: MDPI AG, 2019.
سنة النشر: 2019
مصطلحات موضوعية: 0301 basic medicine, Cancer Research, autophagy, targeted agents, molecular mechanisms, Context (language use), Review, chemotherapy, lcsh:RC254-282, treatment resistance, 03 medical and health sciences, 0302 clinical medicine, Puma, medicine, cancer, Protein kinase B, PI3K/AKT/mTOR pathway, biology, Autophagy, Cancer, chemoresistance, biology.organism_classification, medicine.disease, lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, 3. Good health, 030104 developmental biology, Oncology, Tumor progression, 030220 oncology & carcinogenesis, Cancer research, Signal transduction
الوصف: 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.
اللغة: English
تدمد: 2072-6694
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6497afffb8aee68367fbb47d14b4be24Test
https://www.mdpi.com/2072-6694/11/11/1775Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....6497afffb8aee68367fbb47d14b4be24
قاعدة البيانات: OpenAIRE