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A new duet in cancer biology: AMPK the typical and UBE2O the atypical

Authors
Vila, Isabelle K.Song, Su JungSong, Min Sup
Issue Date
2017
Publisher
TAYLOR & FRANCIS INC
Keywords
AMPK; AMPK alpha 2; arsenite; breast cancer; cancer metabolism; HIF1 alpha; mTOR; prostate cancer; UBE2O; ubiquitination
Citation
MOLECULAR & CELLULAR ONCOLOGY, v.4, no.3
Journal Title
MOLECULAR & CELLULAR ONCOLOGY
Volume
4
Number
3
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/8458
DOI
10.1080/23723556.2017.1304846
ISSN
2372-3556
Abstract
Ubiquitin-conjugating enzyme E2O (UBE2O) is upregulated in human cancers. We have demonstrated that genetic deletion or pharmacological blockade of UBE2O reduces tumorigenesis through inhibiting the mammalian target of rapamycin complex 1-hypoxia-inducible factor 1-alpha pathway. Critically, UBE2O targets adenosine monophosphate (AMP)-activated protein kinase-alpha 2 (AMPK alpha 2) for ubiquitination and degradation. We thus suggest the UBE2O-AMPK alpha 2 axis as a potential therapeutic target for cancer.
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College of Medicine (Department of Biochemistry)
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