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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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HDAC4 Protein Regulates HIF1α Protein Lysine Acetylation and Cancer Cell Response to Hypoxia

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.
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HIF1α Protein Stability Is Increased by Acetylation at Lysine 709

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

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.
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Malate dehydrogenase 2 confers docetaxel resistance via regulations of JNK signaling and oxidative metabolism.

TL;DR: Novel mechanistic understandings in cancer cell chemotherapeutic sensitivity and resistance can optimize treatment and improve patient outcome in prostate cancer therapeutics.
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Interplay between hypoxia and androgen controls a metabolic switch conferring resistance to androgen/AR-targeted therapy.

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.