Title of article :
Resveratrol suppresses the proliferation of breast cancer cells by inhibiting fatty acid synthase signaling pathway
Author/Authors :
Khan، نويسنده , , Arif and Aljarbou، نويسنده , , Ahmad N. and Aldebasi، نويسنده , , Yousef H. and Faisal، نويسنده , , Syed M. and Khan، نويسنده , , Masood A.، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2014
Pages :
8
From page :
765
To page :
772
Abstract :
In breast cancer cells, overexpression of human epidermal growth factor receptor 2 (HER2) increases the translation of fatty acid synthase (FASN) by altering the activity of PI3K/Akt signaling pathways. Cancer chemotherapy causes major side effects and is not effective enough in slowing down the progression of the disease. Earlier studies showed a role for resveratrol in the inhibition of FASN, but the molecular mechanisms of resveratrol-induced inhibition are not known. In the present study, we examined the novel mechanism of resveratrol on Her2-overexpressed breast cancer cells. fect of resveratrol on the growth of breast cancer cells was assessed as percent cell viability by cytotoxicity-based MTT assay and the induction of apoptosis was determined by cell-death detection ELISA and flow cytometric analysis of Annexin-V–PI binding. Western immunobloting was used to detect signaling events in human breast cancer (SKBR-3) cells. howed that resveratrol-mediated down-regulation of FASN and HER2 genes synergistically induced apoptotic death in SKBR-3 cells. This concurrently caused a prominent up-regulation of PEA3, leads to down-regulation of HER2 genes. Resveratrol also alleviated the PI3K/Akt/mTOR signaling by down-regulation of Akt phosphorylation and up-regulation of PTEN expression. findings suggest that resveratrol alters the cell cycle progression and induce cell death via FASN inhibition in HER2 positive breast cancer.
Keywords :
Akt , FASN , HER2 , PI3K , resveratrol , SKBR-3
Journal title :
Cancer Epidemiology
Serial Year :
2014
Journal title :
Cancer Epidemiology
Record number :
1767122
Link To Document :
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