Mitocans Revisited: Mitochondrial Targeting as Efficient Anti-Cancer Therapy
Jazyk angličtina Země Švýcarsko Médium electronic
Typ dokumentu časopisecké články, přehledy
Grantová podpora
DP180103426
Australian Respiratory Council
DP 130101651
Australian Respiratory Council
PubMed
33114695
PubMed Central
PMC7663685
DOI
10.3390/ijms21217941
PII: ijms21217941
Knihovny.cz E-zdroje
- Klíčová slova
- anti-cancer strategy, drug delivery, mitocans, mitochondrial targeting,
- MeSH
- chemorezistence účinky léků MeSH
- cílená molekulární terapie MeSH
- citrátový cyklus účinky léků MeSH
- elektronový transportní řetězec účinky léků metabolismus MeSH
- klinické zkoušky jako téma MeSH
- lidé MeSH
- mitochondrie účinky léků metabolismus MeSH
- nádory farmakoterapie metabolismus MeSH
- oxidace-redukce účinky léků MeSH
- progrese nemoci MeSH
- protinádorové látky farmakologie terapeutické užití MeSH
- regulace genové exprese u nádorů účinky léků MeSH
- signální transdukce účinky léků MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- přehledy MeSH
- Názvy látek
- elektronový transportní řetězec MeSH
- protinádorové látky MeSH
Mitochondria are essential cellular organelles, controlling multiple signalling pathways critical for cell survival and cell death. Increasing evidence suggests that mitochondrial metabolism and functions are indispensable in tumorigenesis and cancer progression, rendering mitochondria and mitochondrial functions as plausible targets for anti-cancer therapeutics. In this review, we summarised the major strategies of selective targeting of mitochondria and their functions to combat cancer, including targeting mitochondrial metabolism, the electron transport chain and tricarboxylic acid cycle, mitochondrial redox signalling pathways, and ROS homeostasis. We highlight that delivering anti-cancer drugs into mitochondria exhibits enormous potential for future cancer therapeutic strategies, with a great advantage of potentially overcoming drug resistance. Mitocans, exemplified by mitochondrially targeted vitamin E succinate and tamoxifen (MitoTam), selectively target cancer cell mitochondria and efficiently kill multiple types of cancer cells by disrupting mitochondrial function, with MitoTam currently undergoing a clinical trial.
Institute of Biotechnology Czech Academy of Sciences 252 50 Prague West Czech Republic
School of Medical Science Griffith University Southport 4222 Qld Australia
School of Medicine Griffith University Southport 4222 Qld Australia
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