SESN2 Knockdown Increases Betulinic Acid-Induced Radiosensitivity of Hypoxic Breast Cancer Cells
Authors:
- Antje GüttlerAGAntje Güttler
- Claus WeinholdtClaus Weinholdt
- Elisabeth RuffERElisabeth Ruff
- Judith ReidtJRJudith Reidt
- Elisa DarnstaedtEDElisa Darnstaedt
- Alicia WildemannAWAlicia Wildemann
- Marina PetrenkoMPMarina Petrenko
- Jacqueline KeßlerJKJacqueline Keßler
- Matthias KapplerMKMatthias Kappler
- Ivo GrosseIvo Grosse
- Dirk VordermarkDVDirk Vordermark
- Matthias BacheMBMatthias Bache
Open Access
Abstract
Betulinic acid (BA) is a natural compound well known for its anti-inflammatory, anti-viral, anti-bacterial, anti-malarial effects and anti-tumor properties. Its enhanced cytotoxicity in tumor cells and induction of cell death in various cancer entities qualifies BA as an interesting candidate for novel treatment concepts. Our analyses showed enhanced cytotoxicity and radiosensitization under hypoxic conditions in human breast cancer cells. So far, the underlying mechanisms are unknown. Therefore, we investigated the BA-treated human breast cancer cell lines MDA-MB-231 and MCF-7 under normoxic and hypoxic conditions based on microarray technology. Hypoxia and BA regulated a variety of genes in both breast cancer cell lines. KEGG pathway analysis identified an enrichment of the p53 pathway in MCF-7 cells (wtp53) under hypoxia. In MDA-MB-231 cells (mtp53) an additional BA incubation was required to activate the p53 signaling pathway. Fourteen down-regulated and up-regulated genes of the p53 pathway were selected for further validation via qRT-PCR in a panel of five breast cancer cell lines. The stress-induced gene Sestrin-2 (SESN2) was identified as one of the most strongly up-regulated genes after BA treatment. Knockdown of SESN2 enhanced BA-induced ROS production, DNA damage, radiosensitivity and reduced autophagy in breast cancer cells. Our results identified SESN2 as an important target to enhance the radiobiological and anti-tumor effects of BA on breast cancer cells.Keywords
Funding Information
- Deutsche Forschungsgemeinschaft (DFG) (410899006 (BA 4877/3, GR 3526/11, VO 871/6))
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