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Yueming Zhu

Researcher at Northwestern University

Publications -  19
Citations -  936

Yueming Zhu is an academic researcher from Northwestern University. The author has contributed to research in topics: Mitochondrion & Acetylation. The author has an hindex of 13, co-authored 19 publications receiving 695 citations.

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SIRT3 deacetylates and increases pyruvate dehydrogenase activity in cancer cells.

TL;DR: The results suggest that the acetylation of PDHA1 provides another layer of enzymatic regulation, in addition to phosphorylation, involving a reversible acetyllysine, suggesting that theacetylome, as well as the kinome, links glycolysis to respiration.
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Loss of NAD-Dependent Protein Deacetylase Sirtuin-2 Alters Mitochondrial Protein Acetylation and Dysregulates Mitophagy.

TL;DR: Findings support that SIRT2 functions as a mitochondrial sirtuin, as well as a regulator of autophagy/mitophagy to maintain mitochondrial biology, thus facilitating cell survival, and for the first time it is shown that Sirt2 directs mitochondrial metabolism.
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SIRT2-Mediated Deacetylation and Tetramerization of Pyruvate Kinase Directs Glycolysis and Tumor Growth.

TL;DR: It is argued that loss of SIRT2 function in cancer cells reprograms their glycolytic metabolism via PKM2 regulation, partially explaining the tumor-permissive phenotype of mice lacking Sirt2 Cancer Res; 76(13); 3802-12.
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Polychlorinated-biphenyl-induced oxidative stress and cytotoxicity can be mitigated by antioxidants after exposure

TL;DR: The hypothesis that exposure of exponentially growing human breast and prostate epithelial cells to PCBs causes increased steady-state levels of intracellular O(2)(*-) and H(2)O(2), induction of MnSOD or CuZnSOD activity, and clonogenic cell killing that could be inhibited by a clinically relevant thiol antioxidant, NAC, as well as by catalase and superoxide dismutase after PCB exposure are supported.
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Manganese superoxide dismutase (SOD2): is there a center in the universe of mitochondrial redox signaling?

TL;DR: How H2O2 formation in mitochondria depends on and is controlled by MnSOD is discussed and why a better understanding of redox hubs in the mitochondria will likely lead to new and improved therapeutics of a number of diseases, including cancer.