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The expression of p21 is upregulated by forkhead box A1/2 in p53-null H1299 cells

Authors
An, Joo-HeeJang, Sang-MinKim, Jung-WoongKim, Chul-HongSong, Peter I.Choi, Kyung-Hee
Issue Date
Nov-2014
Publisher
ELSEVIER SCIENCE BV
Keywords
Transcription factor FOXA1/2; p21; Trichostatin A; Target gene; p53-Independent pathway
Citation
FEBS LETTERS, v.588, no.21, pp 4065 - 4070
Pages
6
Journal Title
FEBS LETTERS
Volume
588
Number
21
Start Page
4065
End Page
4070
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/11607
DOI
10.1016/j.febslet.2014.09.033
ISSN
0014-5793
1873-3468
Abstract
The expression of the cell cycle inhibitor p21 is increased in response to various stimuli and stress signals through p53-dependent and independent pathways. We demonstrate in this study that forkhead box A1/2 (FOXA1/2) is a crucial transcription factor in the activation of p21 transcription via direct binding to the p21 promoter in p53-null H1299 lung carcinoma cells. In addition, histone deacetylase inhibitor trichostatin A (TSA)-mediated upregulation of p21 expression was repressed by knockdown of FOXA1/2 in H1299 cells. Consequently, these results suggest that FOXA1/2 is required for p53-independent p21 expression. (C) 2014 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
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자연과학대학 (생명과학과)
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