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Hui Yang

Researcher at Fudan University

Publications -  34
Citations -  6365

Hui Yang is an academic researcher from Fudan University. The author has contributed to research in topics: Innate immune system & Medicine. The author has an hindex of 17, co-authored 26 publications receiving 4927 citations. Previous affiliations of Hui Yang include University of Texas Southwestern Medical Center.

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Oncometabolite 2-Hydroxyglutarate Is a Competitive Inhibitor of α-Ketoglutarate-Dependent Dioxygenases

TL;DR: 2-HG is a competitive inhibitor of multiple α-KG-dependent dioxygenases, including histone demethylases and the TET family of 5-methlycytosine (5mC) hydroxylases, leading to genome-wide histone and DNA methylation alterations.
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Inhibition of α-KG-dependent histone and DNA demethylases by fumarate and succinate that are accumulated in mutations of FH and SDH tumor suppressors

TL;DR: This study suggests that tumor-derived FH and SDH mutations accumulate fumarate and succinate, leading to enzymatic inhibition of multiple α-KG-dependent dioxygenases and consequent alterations of genome-wide histone and DNA methylation.
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cGAS is essential for cellular senescence

TL;DR: It is shown that cGAS mediates cellular senescence and retards immortalization, a cytosolic DNA sensor that activates innate immunity, which is distinct from, and complementary to, the role ofcGAS in activating antitumor immunity.
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Autophagy induction via STING trafficking is a primordial function of the cGAS pathway.

TL;DR: It is reported that cGAMP-induced autophagy is important for the clearance of DNA and viruses in the cytosol and Interestingly, STING from the sea anemone Nematostella vectensis inducesAutophagy but not interferons in response to stimulation by cGamp, which suggests that induction of autophileagy is a primordial function of the cGAS–STING pathway.
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Tumor development is associated with decrease of TET gene expression and 5-methylcytosine hydroxylation

TL;DR: The levels of 5hmC are dramatically reduced in human breast, liver, lung, pancreatic and prostate cancers when compared with the matched surrounding normal tissues and the substantial reduction of the expression of all three TET genes is revealed, revealing a possible mechanism for the reduced5hmC in cancer cells.