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Ki Yun Kim

Researcher at UPRRP College of Natural Sciences

Publications -  7
Citations -  76

Ki Yun Kim is an academic researcher from UPRRP College of Natural Sciences. The author has contributed to research in topics: Jurkat cells & Apoptosis. The author has an hindex of 5, co-authored 7 publications receiving 50 citations.

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Kaempferol Activates G₂-Checkpoint of the Cell Cycle Resulting in G₂-Arrest and Mitochondria-Dependent Apoptosis in Human Acute Leukemia Jurkat T Cells.

TL;DR: Results demonstrate that kaempferol-mediated antitumor activity toward Jurkat T cells was attributable to G2-checkpoint activation, which caused not only G1-arrest of the cell cycle but also activating phosphorylation of p53 (Ser-15) and subsequent induction of mitochondriadependent apoptotic events, including Bak and PUMA upregulation, Bak activation, Δpsim loss, and caspase cascade activation.
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l-Serine protects mouse hippocampal neuronal HT22 cells against oxidative stress-mediated mitochondrial damage and apoptotic cell death

TL;DR: It is demonstrated that l-serine can protect neuronal cells against oxidative stress-mediated apoptotic cell death by contributing to intracellular antioxidant GSH synthesis and maintaining the mitochondrial fusion-fission balance.
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Enhancement of Quercetin-Induced Apoptosis by Cotreatment with Autophagy Inhibitor Is Associated with Augmentation of BAK-Dependent Mitochondrial Pathway in Jurkat T Cells.

TL;DR: Cotreatment with the autophagy inhibitor resulted in a significant enhancement of quercetin-induced BAK activation and subsequently the mitochondrial damage-mediated apoptosis pathway by augmenting the downregulation of BAG3 and MCL-1 levels in J/Neo cells.
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Phenolic Constituents and Their Anti-inflammatory Activity from Echinochloa utilis Grains

TL;DR: In this paper, seven phenolic compounds including p-coumaric acid, 4-hydroxybenzoic acid and vanillic acid were isolated from the methylene chloride and ethyl acetate fractions of Echinochloa utilis grains.
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Inhibition of autophagy enhances dynamin inhibitor-induced apoptosis via promoting Bak activation and mitochondrial damage in human Jurkat T cells.

TL;DR: Results indicate that MiTMAB-caused cytokinesis failure leads to concomitant induction of apoptosis and cytoprotective autophagy, and suggest that inhibition of autophagic responses is a promising strategy to augment antitumor activity of MiT MAB.