Article

Slug regulates Cyclin D1 expressionin by ubiquitin-proteasome pathway in prostate cancer cells.

Department of Urology, Huashan Hospital, Fudan University, Shanghai, China.
Panminerva medica (impact factor: 1.11). 09/2012; 54(3):219-23. pp.219-23
Source: PubMed

ABSTRACT Cyclin D1 is an important cell cycle regulatory proteins, which is a functional target of Slug in the regulation of cell growth of prostate cancer cells. But the pathway of these two factors interacting with each other is unclear.
The infectde PCa Cells were treated with proteasome inhibitor MG-132. Expression level of Slug, HA-cyclin D1 and other protein was examined by Western blot.
Increasing doses of adenovirus expressing human Slug were added to DU-145 cells separately, but there were no significantly difference on expressions of Slug and cyclin D1. We found that the protein expressions of HA-Cyclin D1 (wide-type) were all reduced through high expression of Slug, which is dose-dependent. However, there is no change for HA-Cyclin D1 (mutant) expression in PC-3 with pMIGW-Cyclin D1-HA T286A. The protein expression of HA-Cyclin D1 were all reduced three days after infection by adding adenovirus expressing human Slug to PC-3 carrying pMIGW-Cyclin D1-HA vector compared to negative control, which is dose-dependent. However, there is no change for HA-Cyclin D1 expression in PC-3 with pMIGW-Cyclin D1-HA treated by MG-132.
We found that forced expression of Slug inhibited proliferation of prostate cancer cells through downregulation of cyclin D1 expression. And Slug regulates cyclin D1 expressionin by ubiquitin-proteasome pathway in PCa cells.

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Keywords

cell growth
 
Cyclin D1
 
cyclin D1 expression
 
Expression level
 
forced expression
 
HA-cyclin D1
 
HA-Cyclin D1 expression
 
human Slug
 
Increasing doses
 
infectde PCa Cells
 
PCa cells
 
pMIGW-Cyclin D1-HA T286A
 
pMIGW-Cyclin D1-HA vector
 
prostate cancer cells
 
proteasome inhibitor MG-132
 
protein expression
 
Slug inhibited proliferation
 
Slug regulates cyclin D1 expressionin
 
two factors interacting
 
ubiquitin-proteasome pathway