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      Mitophagy in Cancer: A Tale of Adaptation

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          Abstract

          In the past years, we have learnt that tumors co-evolve with their microenvironment, and that the active interaction between cancer cells and stromal cells plays a pivotal role in cancer initiation, progression and treatment response. Among the players involved, the pathways regulating mitochondrial functions have been shown to be crucial for both cancer and stromal cells. This is perhaps not surprising, considering that mitochondria in both cancerous and non-cancerous cells are decisive for vital metabolic and bioenergetic functions and to elicit cell death. The central part played by mitochondria also implies the existence of stringent mitochondrial quality control mechanisms, where a specialized autophagy pathway (mitophagy) ensures the selective removal of damaged or dysfunctional mitochondria. Although the molecular underpinnings of mitophagy regulation in mammalian cells remain incomplete, it is becoming clear that mitophagy pathways are intricately linked to the metabolic rewiring of cancer cells to support the high bioenergetic demand of the tumor. In this review, after a brief introduction of the main mitophagy regulators operating in mammalian cells, we discuss emerging cell autonomous roles of mitochondria quality control in cancer onset and progression. We also discuss the relevance of mitophagy in the cellular crosstalk with the tumor microenvironment and in anti-cancer therapy responses.

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          Most cited references238

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          On the origin of cancer cells.

          O WARBURG (1956)
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            Nix is a selective autophagy receptor for mitochondrial clearance.

            Autophagy is the cellular homeostatic pathway that delivers large cytosolic materials for degradation in the lysosome. Recent evidence indicates that autophagy mediates selective removal of protein aggregates, organelles and microbes in cells. Yet, the specificity in targeting a particular substrate to the autophagy pathway remains poorly understood. Here, we show that the mitochondrial protein Nix is a selective autophagy receptor by binding to LC3/GABARAP proteins, ubiquitin-like modifiers that are required for the growth of autophagosomal membranes. In cultured cells, Nix recruits GABARAP-L1 to damaged mitochondria through its amino-terminal LC3-interacting region. Furthermore, ablation of the Nix:LC3/GABARAP interaction retards mitochondrial clearance in maturing murine reticulocytes. Thus, Nix functions as an autophagy receptor, which mediates mitochondrial clearance after mitochondrial damage and during erythrocyte differentiation.
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              Mitochondrial transfer between cells can rescue aerobic respiration.

              Current theory indicates that mitochondria were obtained 1.5 billion years ago from an ancient prokaryote. The mitochondria provided the capacity for aerobic respiration, the creation of the eukaryotic cell, and eventually complex multicellular organisms. Recent reports have found that mitochondria play essential roles in aging and determining lifespan. A variety of heritable and acquired diseases are linked to mitochondrial dysfunction. We report here that mitochondria are more dynamic than previously considered: mitochondria or mtDNA can move between cells. The active transfer from adult stem cells and somatic cells can rescue aerobic respiration in mammalian cells with nonfunctional mitochondria.
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                Author and article information

                Journal
                Cells
                Cells
                cells
                Cells
                MDPI
                2073-4409
                22 May 2019
                May 2019
                : 8
                : 5
                : 493
                Affiliations
                [1 ]Laboratory of Cell Death Research and Therapy, Department for Cellular and Molecular Medicine, Campus Gasthuisberg, University of Leuven (KU Leuven), Herestraat 49, B-3000 Leuven, Belgium; monica.varaperez@ 123456kuleuven.vib.be (M.V.-P.); blanca.felipeabrio@ 123456kuleuven.vib.be (B.F.-A.)
                [2 ]Laboratory of Cell Death Research and Therapy, VIB-KU Leuven Center for Cancer Biology, 3000 Leuven, Belgium
                Author notes
                [* ]Correspondence: patrizia.agostinis@ 123456kuleuven.vib.be ; Tel.: +32-16-33-0650
                Article
                cells-08-00493
                10.3390/cells8050493
                6562743
                31121959
                a4ccca25-c845-43d9-b17f-3a34ddce89da
                © 2019 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 02 May 2019
                : 21 May 2019
                Categories
                Review

                mitophagy,mitochondria,autophagy,cancer,tumor microenvironment,anti-cancer therapy resistance,mitochondrial dynamics

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