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Updated: Nov 27, 2025

In Vitro and In Vivo Detection of Mitophagy in Human Cells, C. Elegans, and Mice
Published on: November 22, 2017
Mitophagy Receptors in Tumor Biology
Yangchun Xie1, Jiao Liu2, Rui Kang3
1Department of Oncology, The Second Xiangya Hospital, Central South University, Changsha, China.
Abstract:
Mitochondria are multifunctional organelles that regulate cancer biology by synthesizing macromolecules, producing energy, and regulating cell death. The understanding of mitochondrial morphology, function, biogenesis, fission and fusion kinetics, and degradation is important for the development of new anticancer strategies. Mitophagy is a type of selective autophagy that can degrade damaged mitochondria under various environmental stresses, especially oxidative damage and hypoxia. The key regulator of mitophagy is the autophagy receptor, which recognizes damaged mitochondria and allows them to enter autophagosomes by binding to MAP1LC3 or GABARAP, and then undergo lysosomal-dependent degradation. Many components of mitochondria, including mitochondrial membrane proteins (e.g., PINK1, BNIP3L, BNIP3, FUNDC1, NIPSNAP1, NIPSNAP2, BCL2L13, PHB2, and FKBP8) and lipids (e.g., cardiolipin and ceramides), act as mitophagy receptors in a context-dependent manner. Dysfunctional mitophagy not only inhibits, but also promotes, tumorigenesis. Similarly, mitophagy plays a dual role in chemotherapy, radiotherapy, and immunotherapy. In this review, we summarize the latest advances in the mechanisms of mitophagy and highlight the pathological role of mitophagy receptors in tumorigenesis and treatment.
Insights
Mitophagy, the degradation of damaged mitochondria, is crucial in cancer. Autophagy receptors regulate this process, and their dysfunction impacts tumor growth and treatment response.
Area of Science:
- Mitochondrial biology
- Cellular degradation pathways
- Cancer research
Background:
- Mitochondria are vital organelles involved in energy production, macromolecule synthesis, and cell death regulation.
- Understanding mitochondrial dynamics, including mitophagy, is key for developing novel anticancer strategies.
- Mitophagy, a selective form of autophagy, removes damaged mitochondria, particularly under stress conditions like hypoxia and oxidative damage.
Purpose of the Study:
- To review the latest advancements in mitophagy mechanisms.
- To highlight the role of mitophagy receptors in cancer development and treatment.
Main Methods:
- Literature review of current research on mitophagy.
- Analysis of the function of autophagy receptors in mitochondrial degradation.
- Examination of the dual role of mitophagy in tumorigenesis and cancer therapy.
Main Results:
- Autophagy receptors, including mitochondrial proteins and lipids, mediate mitophagy in a context-dependent manner.
- Dysfunctional mitophagy can either inhibit or promote tumor formation.
- Mitophagy exhibits a dual role in the efficacy of chemotherapy, radiotherapy, and immunotherapy.
Conclusions:
- Mitophagy receptors are critical regulators of mitochondrial quality control with significant implications in cancer.
- Targeting mitophagy pathways and receptors presents a promising avenue for cancer treatment strategies.
- Further research into mitophagy mechanisms is essential for advancing cancer therapy.
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