Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/57759
Title: Akt2 and p-Akt overexpression in oral cancer cells is due to a reduced rate of protein degradation
Authors: Prakasit Archewa
Supansa Pata
Pareena Chotjumlong
Chayarop Supanchart
Suttichai Krisanaprakornkit
Anak Iamaroon
Keywords: Medicine
Issue Date: 1-Feb-2017
Abstract: © 2015 Wiley Publishing Asia Pty Ltd. OBJECTIVE: To quantitatively measure the increased expression of Akt2 and its phosphorylated form (p-Akt) in oral cancer cell lines and investigate the post-translational mechanism for Akt2 and p-Akt overexpression.METHODS: Three oral cancer cell lines and three cell lines of primary human oral keratinocytes (HOKs) were cultured and the degrees of Akt2 and p-Akt expression was evaluated by immunoblot analysis and flow cytometry. Each cell line was incubated with cycloheximide, an inhibitor of new protein synthesis, for various times to quantitatively determine the remaining expression levels of Akt2 and p-Akt by flow cytometry. The localization of Akt2 and p-Akt was assessed by immunofluorescence.RESULTS: The levels of Akt2 and p-Akt proteins were significantly higher in cancer cell lines than those in HOKs (P < 0.05). When the new protein synthesis was blocked by cycloheximide treatment, the degradation rate of Akt2 and p-Akt in oral cancer cells was significantly lower than that in HOKs (P < 0.05). Both Akt2 and p-Akt were more intensely stained in the cytoplasm of cancer cells, whereas HOKs expressed Akt2 and p-Akt only minimally.CONCLUSION: Both Akt2 and p-Akt were overexpressed in oral cancer cells, which may be partly explained by a reduced rate of protein degradation in order to maintain high cytosolic levels.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85041897611&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/57759
ISSN: 20411626
Appears in Collections:CMUL: Journal Articles

Files in This Item:
There are no files associated with this item.


Items in CMUIR are protected by copyright, with all rights reserved, unless otherwise indicated.