Prof Federica Sotgia F.Sotgia@salford.ac.uk
A mitochondrial based oncology platform for targeting cancer stem cells (CSCs) : MITO-ONC-RX
Sotgia, F; Ozsvari, B; Fiorillo, M; De Francesco, EM; Bonuccelli, G; Lisanti, MP
Authors
B Ozsvari
M Fiorillo
EM De Francesco
G Bonuccelli
Prof Michael Lisanti M.P.Lisanti@salford.ac.uk
Abstract
Here, we wish to propose a new systematic approach to cancer therapy, based on the targeting of mitochondrial metabolism, especially in cancer stem cells (CSCs). In the future, we envision that anti-mitochondrial therapy would ultimately be practiced as an add-on to more conventional therapy, largely for the prevention of tumor recurrence and cancer metastasis. This mitochondrial based oncology platform would require a panel of FDA-approved therapeutics (e.g. Doxycycline) that can safely be used to inhibit mitochondrial OXPHOS and/or biogenesis in CSCs. In addition, new therapeutics that target mitochondria could also be developed, to optimize their ability to eradicate CSCs. Finally, in this context, mitochondrial-based biomarkers (i.e. “Mito-signatures”) could be utilized as companion diagnostics, to identify high-risk cancer patients at diagnosis, facilitating the early detection of tumor recurrence and the prevention of treatment failure. In summary, we suggest that new clinical trials are warranted to test and possibly implement this emerging treatment strategy, in a variety of human cancer types. This general approach, using FDA-approved antibiotics to target mitochondria, was effective in killing CSCs originating from many different cancer types, including DCIS, breast (ER(+) and ER(-)), prostate, ovarian, lung and pancreatic cancers, as well as melanoma and glioblastoma, among others. Thus, we propose the term MITO-ONC-RX, to describe this anti-mitochondrial platform for targeting CSCs. The use of re-purposed FDA-approved drugs will undoubtedly help to accelerate the clinical evaluation of this approach, as these drugs can move directly into Phase II clinical trials, saving considerable amounts of time (10–15 y) and billions in financial resources.
Citation
Sotgia, F., Ozsvari, B., Fiorillo, M., De Francesco, E., Bonuccelli, G., & Lisanti, M. (2018). A mitochondrial based oncology platform for targeting cancer stem cells (CSCs) : MITO-ONC-RX. Cell Cycle, 17(17), 2091-2100. https://doi.org/10.1080/15384101.2018.1515551
Journal Article Type | Article |
---|---|
Acceptance Date | Aug 20, 2018 |
Online Publication Date | Sep 26, 2018 |
Publication Date | Sep 26, 2018 |
Deposit Date | Oct 2, 2018 |
Publicly Available Date | Oct 2, 2018 |
Journal | Cell Cycle |
Print ISSN | 1538-4101 |
Electronic ISSN | 1551-4005 |
Publisher | Taylor and Francis |
Volume | 17 |
Issue | 17 |
Pages | 2091-2100 |
DOI | https://doi.org/10.1080/15384101.2018.1515551 |
Publisher URL | https://doi.org/10.1080/15384101.2018.1515551 |
Related Public URLs | https://www.tandfonline.com/toc/kccy20/current |
Files
A mitochondrial based oncology platform for targeting cancer stem cells CSCs MITO ONC RX.pdf
(2.4 Mb)
PDF
Licence
http://creativecommons.org/licenses/by-nc-nd/4.0/
Publisher Licence URL
http://creativecommons.org/licenses/by-nc-nd/4.0/
You might also like
Downloadable Citations
About USIR
Administrator e-mail: library-research@salford.ac.uk
This application uses the following open-source libraries:
SheetJS Community Edition
Apache License Version 2.0 (http://www.apache.org/licenses/)
PDF.js
Apache License Version 2.0 (http://www.apache.org/licenses/)
Font Awesome
SIL OFL 1.1 (http://scripts.sil.org/OFL)
MIT License (http://opensource.org/licenses/mit-license.html)
CC BY 3.0 ( http://creativecommons.org/licenses/by/3.0/)
Powered by Worktribe © 2024
Advanced Search