Abstract | PURPOSE: METHODS: T47D cells were stimulated with MTE at concentrations of 5, 10 and 50 µg/ml. Cell viability was assessed using a WST-1 assay after an incubation time of 72 h. PPARγ expression was quantified at the gene level by real-time polymerase chain reaction (PCR). A western blot (WB) was carried out for the qualitative assessment of the expression behavior of on a protein level. RESULTS: The WST-1 test showed a significant inhibition of viability in T47D cells after 72 h at 5, 10 and 50 µg/ml. The PCR showed an overexpression of PPARγ in T47D cells in all concentrations. At the concentration of 50 µg/ml the expression was significantly increased (p < 0.05). The WB demonstrated a significant quantitative increase of PPARγ at protein level with MTE concentrations of 10 and 50 µg/ml. In addition, there was a negative correlation between the overexpression of PPAR γ and the inhibition of proliferation. CONCLUSION: MTE decreases the cell viability of T47D cells and furthermore leads to an overexpression of PPARγ on protein and mRNA level.
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Authors | Simon Keckstein, Constantin Tilgener, Udo Jeschke, Simone Hofmann, Theresa Vilsmaier, Till Kaltofen, Helene Heidegger, Falk Batz, Sven Mahner, Lennard Schröder |
Journal | Archives of gynecology and obstetrics
(Arch Gynecol Obstet)
Vol. 306
Issue 2
Pg. 451-459
(08 2022)
ISSN: 1432-0711 [Electronic] Germany |
PMID | 35079875
(Publication Type: Journal Article)
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Copyright | © 2022. The Author(s). |
Chemical References |
- PPAR gamma
- Plant Extracts
- RNA, Messenger
- Tea
|
Topics |
- Breast Neoplasms
(drug therapy)
- Cell Survival
- Female
- Humans
- PPAR gamma
(genetics)
- Plant Extracts
(pharmacology)
- RNA, Messenger
(genetics)
- Tea
|