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Positive feedback regulation between Akt phosphorylation and fatty acid synthase expression in osteosarcoma.

Authors :
Wang H
Luo QF
Peng AF
Long XH
Wang TF
Liu ZL
Zhang GM
Zhou RP
Gao S
Zhou Y
Chen WZ
Source :
International journal of molecular medicine [Int J Mol Med] 2014 Mar; Vol. 33 (3), pp. 633-9. Date of Electronic Publication: 2013 Dec 23.
Publication Year :
2014

Abstract

The activation of PI3K/Akt and the overexpression of fatty acid synthase (FASN) are frequently observed in human osteosarcoma (OS). In the present study, in order to investigate the possible association between the phosphorylation of Akt and FASN expression, immunohistochemical staining was conducted on 24 OS specimens from patients with pulmonary metastasis, which revealed a significant positive correlation between phosphorylated Akt (p-Akt) and the expression of FASN (R=0.469, P=0.04). To investigate the association between p-Akt and FASN in vitro, human U2-OS OS cells were treated with FASN-specific RNAi plasmid or LY294002 (an inhibitor of PI3k/Akt). The mRNA levels of Akt and FASN were measured by real-time PCR. Western blot analysis was also performed to detect the protein experession of PI3K, Akt, p-Akt and FASN. The results demonstrated that the PI3K/Akt signaling pathway modulates FASN expression; the inhibition of FASN resulted in the downregulation of p-Akt in the U2-OS cells. Furthermore, the effects induced by the inhibition of the activity of p-Akt or FASN on the malignant phenotype of U2-OS cells were investigated, demonstrating that the malignant phenotype was inhibited by suppressing the activity of PI3K/Akt or FASN in the U2-OS cells. The findings from our study suggest the existence of a positive feedback regulation between Akt phosphorylation and FASN expression and that this loop may play an important role in the malignant phenotype of OS cells.

Details

Language :
English
ISSN :
1791-244X
Volume :
33
Issue :
3
Database :
MEDLINE
Journal :
International journal of molecular medicine
Publication Type :
Academic Journal
Accession number :
24366211
Full Text :
https://doi.org/10.3892/ijmm.2013.1602