TY - JOUR
T1 - Chemical mitophagy modulators
T2 - Drug development strategies and novel regulatory mechanisms
AU - Dong, Yu
AU - Zhuang, Xu Xu
AU - Wang, Yi Ting
AU - Tan, Jieqiong
AU - Feng, Du
AU - Li, Min
AU - Zhong, Qing
AU - Song, Zhiyin
AU - Shen, Han Ming
AU - Fang, Evandro F.
AU - Lu, Jia Hong
N1 - Jiahong Lu is supported by the National Natural Science Foundation of China (No. 82271455), the University of Macau grants (No. MYRG2022–00094-ICMS), the Guangdong Basic and Applied Basic Research Foundation (No. 2022A1515012416), the Science and Tech- nology Development Fund, Macau SAR (No. 0128/2019/A3), and the Shenzhen Fundamental Research Program (No. SGDX20210823103804030). Evandro Fei Fang is supported by Cure Alzheimer’s Fund (#282952), HELSE SØR-ØST (#2020001, #2021021, #2023093), the Research Council of Norway (#262175, #334361), Molecule AG/VITADAO (#282942), NordForsk Foundation (#119986), Akershus University Hospital (#269901, #261973, #262960), the Civitan Norges Forskningsfond for Alzheimers sykdom (#281931), the Czech Republic-Norway KAPPA programme (with Martin Vyhn´alek, #TO01000215), and the Rosa sløyfe/Norwegian Cancer Society & Norwegian Breast Cancer Society (#207819)
Publisher Copyright:
© 2023 The Authors
PY - 2023/8
Y1 - 2023/8
N2 - Maintaining mitochondrial homeostasis is a potential therapeutic strategy for various diseases, including neurodegenerative diseases, cardiovascular diseases, metabolic disorders, and cancer. Selective degradation of mitochondria by autophagy (mitophagy) is a fundamental mitochondrial quality control mechanism conserved from yeast to humans. Indeed, small-molecule modulators of mitophagy are valuable pharmaceutical tools that can be used to dissect complex biological processes and turn them into potential drugs. In the past few years, pharmacological regulation of mitophagy has shown promising therapeutic efficacy in various disease models. However, with the increasing number of chemical mitophagy modulator studies, frequent methodological flaws can be observed, leading some studies to draw unreliable or misleading conclusions. This review attempts (a) to summarize the molecular mechanisms of mitophagy; (b) to propose a Mitophagy Modulator Characterization System (MMCS); (c) to perform a comprehensive analysis of methods used to characterize mitophagy modulators, covering publications over the past 20 years; (d) to provide novel targets for pharmacological intervention of mitophagy. We believe this review will provide a panorama of current research on chemical mitophagy modulators and promote the development of safe and robust mitophagy modulators with therapeutic potential by introducing high methodological standards.
AB - Maintaining mitochondrial homeostasis is a potential therapeutic strategy for various diseases, including neurodegenerative diseases, cardiovascular diseases, metabolic disorders, and cancer. Selective degradation of mitochondria by autophagy (mitophagy) is a fundamental mitochondrial quality control mechanism conserved from yeast to humans. Indeed, small-molecule modulators of mitophagy are valuable pharmaceutical tools that can be used to dissect complex biological processes and turn them into potential drugs. In the past few years, pharmacological regulation of mitophagy has shown promising therapeutic efficacy in various disease models. However, with the increasing number of chemical mitophagy modulator studies, frequent methodological flaws can be observed, leading some studies to draw unreliable or misleading conclusions. This review attempts (a) to summarize the molecular mechanisms of mitophagy; (b) to propose a Mitophagy Modulator Characterization System (MMCS); (c) to perform a comprehensive analysis of methods used to characterize mitophagy modulators, covering publications over the past 20 years; (d) to provide novel targets for pharmacological intervention of mitophagy. We believe this review will provide a panorama of current research on chemical mitophagy modulators and promote the development of safe and robust mitophagy modulators with therapeutic potential by introducing high methodological standards.
KW - Cancer
KW - Cardiovascular diseases
KW - Drug development
KW - Metabolic disorders
KW - Mitophagy
KW - Neurodegenerative diseases
UR - http://www.scopus.com/inward/record.url?scp=85163445082&partnerID=8YFLogxK
UR - https://www.sciencedirect.com/science/article/pii/S1043661823001913?via%3Dihub
U2 - 10.1016/j.phrs.2023.106835
DO - 10.1016/j.phrs.2023.106835
M3 - Journal article
C2 - 37348691
AN - SCOPUS:85163445082
SN - 1043-6618
VL - 194
JO - Pharmacological Research
JF - Pharmacological Research
M1 - 106835
ER -