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HIF-2 alpha Enhances beta-Catenin/TCF-Driven Transcription by Interacting with beta-Catenin

Cited 59 time in Web of Science Cited 65 time in Scopus
Authors
Choi, Hyunsung; Chun, Yang-Sook; Park, Jong-Wan; Kim, Tae-You
Issue Date
2010-12-15
Publisher
AMER ASSOC CANCER RESEARCH
Citation
CANCER RESEARCH; Vol.70 24; 10101-10111
Abstract
The tumor-promoting factors beta-catenin and hypoxia-inducible factor (HIF) are often found to be coactivated in rapidly growing tumors. Recently, it was shown that HIF-1 alpha negatively regulates Wnt/beta-catenin signaling by sequestering beta-catenin from beta-catenin/T-cell factor (TCF). However, no investigation has been undertaken on the involvement of HIF-2 alpha in beta-catenin regulation. In this study, it was found that, like HIF-1 alpha, HIF-2 alpha interacts with beta-catenin, but at a different site. Furthermore, HIF-2 alpha was found to assemble with beta-catenin/TCF and facilitate gene transcription. Mutational analyses revealed that transactivation domains of HIF-2 alpha promote p300 coactivator recruitment by beta-catenin. Furthermore, HIF-2 alpha and beta-catenin were found to associate in the nuclei of 786-0 renal cell carcinoma cells, and HIF-2 alpha was found to be required for beta-catenin activation in these cells and for their proliferation. These results suggest that this interaction contributes to the unrestrained growth of tumor cells containing coactivated HIF-2 alpha and beta-catenin. Interestingly, these actions of HIF-2 alpha oppose those of HIF-1 alpha on beta-catenin and cell growth, and this suggests that HIF-1 alpha/HIF-2 alpha balance may importantly determine cell growth when hypoxia and Wnt stimulation coexist. Cancer Res; 70(24); 10101-11. (C) 2010 AACR.
ISSN
0008-5472
Language
English
URI
http://hdl.handle.net/10371/76206
DOI
https://doi.org/10.1158/0008-5472.CAN-10-0505
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College of Medicine/School of Medicine (의과대학/대학원)Dept. of Physiology (생리학교실)Journal Papers (저널논문_생리학교실)
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