PMID- 31699565 OWN - NLM STAT- MEDLINE DCOM- 20210728 LR - 20210728 IS - 1879-3061 (Electronic) IS - 1043-2760 (Print) IS - 1043-2760 (Linking) VI - 31 IP - 1 DP - 2020 Jan TI - Pros and Cons of Chaperone-Mediated Autophagy in Cancer Biology. PG - 53-66 LID - S1043-2760(19)30208-5 [pii] LID - 10.1016/j.tem.2019.09.007 [doi] AB - Autophagy contributes to cellular quality control and energetics through lysosomal breakdown and recycling of essential cellular components. Chaperone-mediated autophagy (CMA) adds to these autophagic functions the ability to timely and selectively degrade single tagged proteins to terminate their cellular function and, in this way, participate in the regulation of multiple cellular processes. Many cancer cells upregulate CMA for protumorigenic and prosurvival purposes. However, growing evidence supports a physiological role for CMA in limiting malignant transformation. Understanding the mechanisms behind this functional switch of CMA from antioncogenic to pro-oncogenic is fundamental for targeting CMA in cancer treatment. We summarize current understanding of CMA functions in cancer biology and discuss the basis for its context-dependent dual role in oncogenesis. CI - Copyright (c) 2019 Elsevier Ltd. All rights reserved. FAU - Arias, Esperanza AU - Arias E AD - Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Marion Bessin Liver Research Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, NY 10461, USA. Electronic address: esperanza.arias-perez@einstein.yu.edu. FAU - Cuervo, Ana Maria AU - Cuervo AM AD - Marion Bessin Liver Research Center, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Institute for Aging Studies, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Development and Molecular Biology, Albert Einstein College of Medicine, Bronx, NY 10461, USA. Electronic address: ana-maria.cuervo@einstein.yu.edu. LA - eng GR - U54 NS100717/NS/NINDS NIH HHS/United States GR - R01 AG021904/AG/NIA NIH HHS/United States GR - R01 DK124308/DK/NIDDK NIH HHS/United States GR - R37 AG021904/AG/NIA NIH HHS/United States GR - RF1 AG054108/AG/NIA NIH HHS/United States GR - R01 DK098408/DK/NIDDK NIH HHS/United States GR - P01 AG031782/AG/NIA NIH HHS/United States PT - Journal Article PT - Review DEP - 20191104 PL - United States TA - Trends Endocrinol Metab JT - Trends in endocrinology and metabolism: TEM JID - 9001516 SB - IM MH - Animals MH - Carcinogenesis/metabolism MH - Chaperone-Mediated Autophagy/genetics/*physiology MH - Humans MH - Lysosomes/metabolism MH - Neoplasms/*metabolism/*pathology PMC - PMC7020649 MID - NIHMS1542248 OTO - NOTNLM OT - chaperones OT - lysosomes OT - metabolism OT - oncogenes OT - protein degradation OT - tumorigenesis EDAT- 2019/11/09 06:00 MHDA- 2021/07/29 06:00 PMCR- 2021/01/01 CRDT- 2019/11/09 06:00 PHST- 2019/08/02 00:00 [received] PHST- 2019/09/16 00:00 [revised] PHST- 2019/09/17 00:00 [accepted] PHST- 2019/11/09 06:00 [pubmed] PHST- 2021/07/29 06:00 [medline] PHST- 2019/11/09 06:00 [entrez] PHST- 2021/01/01 00:00 [pmc-release] AID - S1043-2760(19)30208-5 [pii] AID - 10.1016/j.tem.2019.09.007 [doi] PST - ppublish SO - Trends Endocrinol Metab. 2020 Jan;31(1):53-66. doi: 10.1016/j.tem.2019.09.007. Epub 2019 Nov 4.