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Marizomib suppresses triple-negative breast cancer via proteasome and oxidative phosphorylation inhibition
PV. Raninga, A. Lee, D. Sinha, LF. Dong, KK. Datta, X. Lu, P. Kalita-de Croft, M. Dutt, M. Hill, N. Pouliot, H. Gowda, M. Kalimutho, J. Neuzil, KK. Khanna
Jazyk angličtina Země Austrálie
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NV17-30138A
MZ0
CEP - Centrální evidence projektů
Digitální knihovna NLK
Plný text - Článek
NLK
Directory of Open Access Journals
od 2011
Free Medical Journals
od 2011
PubMed Central
od 2011
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od 2011 do 2020
ProQuest Central
od 2019-01-01
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od 2011-01-01
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od 2011-01-01
Health & Medicine (ProQuest)
od 2019-01-01
ROAD: Directory of Open Access Scholarly Resources
od 2011
PubMed
32373211
DOI
10.7150/thno.42705
Knihovny.cz E-zdroje
- MeSH
- apoptóza účinky léků genetika MeSH
- epitelo-mezenchymální tranzice účinky léků genetika MeSH
- inhibitory proteasomu terapeutické užití MeSH
- laktony terapeutické užití MeSH
- lidé MeSH
- myši MeSH
- nádorové buněčné linie MeSH
- oxidativní fosforylace účinky léků MeSH
- proliferace buněk účinky léků genetika MeSH
- proteasomový endopeptidasový komplex účinky léků metabolismus MeSH
- protinádorové látky terapeutické užití MeSH
- pyrroly terapeutické užití MeSH
- triple-negativní karcinom prsu farmakoterapie genetika metabolismus MeSH
- xenogenní modely - testy protinádorové aktivity MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Purpose: Lacking effective targeted therapies, triple-negative breast cancer (TNBCs) is highly aggressive and metastatic disease, and remains clinically challenging breast cancer subtype to treat. Despite the survival dependency on the proteasome pathway genes, FDA-approved proteasome inhibitors induced minimal clinical response in breast cancer patients due to weak proteasome inhibition. Hence, developing effective targeted therapy using potent proteasome inhibitor is required. Methods: We evaluated anti-cancer activity of a potent proteasome inhibitor, marizomib, in vitro using breast cancer lines and in vivo using 4T1.2 murine syngeneic model, MDA-MB-231 xenografts, and patient-derived tumor xenografts. Global proteome profiling, western blots, and RT-qPCR were used to investigate the mechanism of action for marizomib. Effect of marizomib on lung and brain metastasis was evaluated using syngeneic 4T1BR4 murine TNBC model in vivo. Results: We show that marizomib inhibits multiple proteasome catalytic activities and induces a better anti-tumor response in TNBC cell lines and patient-derived xenografts alone and in combination with the standard-of-care chemotherapy. Mechanistically, we show that marizomib is a dual inhibitor of proteasome and oxidative phosphorylation (OXPHOS) in TNBCs. Marizomib reduces lung and brain metastases by reducing the number of circulating tumor cells and the expression of genes involved in the epithelial-to-mesenchymal transition. We demonstrate that marizomib-induced OXPHOS inhibition upregulates glycolysis to meet the energetic demands of TNBC cells and combined inhibition of glycolysis with marizomib leads to a synergistic anti-cancer activity. Conclusions: Our data provide a strong rationale for a clinical evaluation of marizomib in primary and metastatic TNBC patients.
Institute of Biotechnology Czech Academy of Sciences Prague West 252 50 Czech Republic
Olivia Newton John Cancer Research Institute 145 Studley Road Heidelberg Vic 3084 Australia
QIMR Berghofer Medical Research Institute 300 Herston Road Herston Brisbane QLD 4006 Australia
School of Medical Science Griffith University Southport QLD 4222 Australia
Citace poskytuje Crossref.org
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