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Gelsolin negatively regulates the activity of tumor suppressor p53 through their physical interaction in hepatocarcinoma HepG2 cells

Authors
An, Joo-HeeKim, Jung-WoongJang, Sang-MinKim, Chul-HongKang, Eun-JinChoi, Kyung-Hee
Issue Date
Aug-2011
Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
Keywords
p53; Apoptosis; Gelsolin; Transcriptional regulation; Protein-protein interaction; Hepatocarcinoma
Citation
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.412, no.1, pp 44 - 49
Pages
6
Journal Title
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
Volume
412
Number
1
Start Page
44
End Page
49
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/21336
DOI
10.1016/j.bbrc.2011.07.034
ISSN
0006-291X
1090-2104
Abstract
As a transcription factor, p53 modulates several cellular responses including cell-cycle control, apoptosis, and differentiation. In this study, we have shown that an actin regulatory protein, gelsolin (GSN), can physically interact with p53. The nuclear localization of p53 is inhibited by GSN overexpression in hepatocarcinoma HepG2 cells. Additionally, we demonstrate that GSN negatively regulates p53-dependent transcriptional activity of a reporter construct, driven by the p21-promoter. Furthermore, p53-mediated apoptosis was repressed in GSN-transfected HepG2 cells. Taken together, these results suggest that GSN binds to p53 and this interaction leads to the inhibition of p53-induced apoptosis by anchoring of p53 in the cytoplasm in HepG2 cells. (C) 2011 Elsevier Inc. All rights reserved.
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Kim, Jung-Woong
자연과학대학 (생명과학과)
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