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Changhui Xue
Researcher at Oregon Health & Science University
Publications - 12
Citations - 588
Changhui Xue is an academic researcher from Oregon Health & Science University. The author has contributed to research in topics: Cancer cell & Regulation of gene expression. The author has an hindex of 8, co-authored 12 publications receiving 448 citations.
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Journal ArticleDOI
HDAC4 Protein Regulates HIF1α Protein Lysine Acetylation and Cancer Cell Response to Hypoxia
Hao Geng,Christopher T. Harvey,Janét Pittsenbarger,Qiong Liu,Tomasz M. Beer,Changhui Xue,David Z. Qian +6 more
TL;DR: The novel biological relationship between HDAC4 and HIF1α presented here suggests a potential role for the deacetylase enzyme in regulating HIF-1 cancer cell response to hypoxia and presents a more specific molecular target of inhibition.
Journal ArticleDOI
HIF1α Protein Stability Is Increased by Acetylation at Lysine 709
Hao Geng,Qiong Liu,Changhui Xue,Larry L. David,Tomasz M. Beer,George Thomas,Mu Shui Dai,David Z. Qian +7 more
TL;DR: A novel biological consequence upon HIF1α-p300 interaction is demonstrated, in which Hif1α can be stabilized by p300 via Lys-709 acetylation, which increases the protein stability and decreases polyubiquitination in both normoxia and hypoxia.
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Identification of a Potent Inhibitor of CREB-Mediated Gene Transcription with Efficacious in Vivo Anticancer Activity
Fuchun Xie,Bingbing X. Li,Alina Kassenbrock,Changhui Xue,Xiaoyan Wang,David Z. Qian,Rosalie C. Sears,Xiangshu Xiao +7 more
TL;DR: Biological evaluations of a series of structural congeners of naphthamide 3a uncovered compound 3i (666-15) as a potent and selective inhibitor of CREB-mediated gene transcription and potently inhibited cancer cell growth without harming normal cells.
Journal ArticleDOI
Malate dehydrogenase 2 confers docetaxel resistance via regulations of JNK signaling and oxidative metabolism.
Qiong Liu,Christopher T. Harvey,Hao Geng,Changhui Xue,Vivian Chen,Tomasz M. Beer,David Z. Qian +6 more
TL;DR: Novel mechanistic understandings in cancer cell chemotherapeutic sensitivity and resistance can optimize treatment and improve patient outcome in prostate cancer therapeutics.
Journal ArticleDOI
Interplay between hypoxia and androgen controls a metabolic switch conferring resistance to androgen/AR-targeted therapy.
Hao Geng,Changhui Xue,Janet Mendonca,Xiao Xin Sun,Qiong Liu,Patrick N. Reardon,Yingxiao Chen,Kendrick Qian,Vivian Hua,Alice P. Chen,Freddy Pan,Julia Yuan,Sang Dang,Tomasz M. Beer,Mu Shui Dai,Sushant Kachhap,David Z. Qian +16 more
TL;DR: It is shown that, under conditions of hypoxia, AR inhibition via enzalutamide increases the expression of the glycolytic enzyme phosphoglucose isomerase (GPI) promoting a metabolic rewiring that allows the cells to survive, and consistent GPI inhibition restores sensitivity to enzalUTamide.