| Literature DB >> 22173032 |
Deresa Lee1, Sang-Joon Park, Ki Sa Sung, Jikyoung Park, Sean Bong Lee, Sang-Yoon Park, Hyo Jeong Lee, Jang-Won Ahn, So Jung Choi, Seok-Geun Lee, Sung-Hoon Kim, Duk-Hwan Kim, Jhingook Kim, Yongsok Kim, Cheol Yong Choi.
Abstract
The Ras effector NORE1 is frequently silenced in primary adenocarcinomas, although the significance of this silencing for tumorigenesis is unclear. Here we show that NORE1 induces polyubiquitination and proteasomal degradation of oncoprotein HIPK1 by facilitating its interaction with the Mdm2 E3 ubiquitin ligase. Endogenous HIPK1 is stabilized in Nore1-deficient mouse embryonic fibroblasts, and depletion of HIPK1 in NORE1-silenced lung adenocarcinoma cells inhibits anchorage-independent cell growth and tumour formation in nude mice. These findings indicate that the control of HIPK1 stability by Mdm2-NORE1 has a major effect on cell behaviour, and epigenetic inactivation of NORE1 enables adenocarcinoma formation in vivo through HIPK1 stabilization.Entities:
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Year: 2012 PMID: 22173032 PMCID: PMC3271333 DOI: 10.1038/embor.2011.235
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807