D
Do Youn Jun
Researcher at UPRRP College of Natural Sciences
Publications - 54
Citations - 775
Do Youn Jun 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 15, co-authored 54 publications receiving 700 citations.
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Apoptogenic activity of auraptene of Zanthoxylum schinifolium toward human acute leukemia Jurkat T cells is associated with ER stress-mediated caspase-8 activation that stimulates mitochondria-dependent or -independent caspase cascade
TL;DR: It is demonstrated that the apoptotic effect of AUR on Jurkat T cells was exerted by the ER stress-mediated activation of caspase-8, and the subsequent induction of mitochondria-dependent or -independent activation ofcaspase cascade, which could be suppressed by Bcl-xL.
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Characterization of human phosphoserine aminotransferase involved in the phosphorylated pathway of L-serine biosynthesis
TL;DR: The results demonstrate that although two isoforms of human PSAT can be produced by alternative splicing, PSAT beta rather than PSAT alpha is the physiologically functional enzyme required for the phosphorylated pathway, and indicate that the humanPSAT gene is regulated depending on tissue specificity as well as cellular proliferation status with a maximum level expression in the S-phase.
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Nucleotide sequence and differential expression of the human 3-phosphoglycerate dehydrogenase gene
TL;DR: It is demonstrated that the human 3-PGDH gene is regulated at the transcriptional level depending on tissue specificty and cellular proliferative status, and its transcriptional regulation mechanism may be a useful target for diagnosis and therapy of cancer.
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Mollugin induces apoptosis in human Jurkat T cells through endoplasmic reticulum stress-mediated activation of JNK and caspase-12 and subsequent activation of mitochondria-dependent caspase cascade regulated by Bcl-xL.
TL;DR: It is demonstrated that mollugin-induced cytotoxicity in Jurkat T cells was mainly attributable to apoptosis provoked via endoplasmic reticulum (ER) stress-mediated activation of JNK and caspase-12, and subsequent mitochondria-dependent activation of caspasing-9 and -3, which could be regulated by Bcl-xL.
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Clinical Implication of Serine Metabolism-Associated Enzymes in Colon Cancer.
Shinkyo Yoon,Jong Gwang Kim,An Na Seo,Soo Yeun Park,Hyejin Kim,Jun Seok Park,Gyu-Seog Choi,Ji Yun Jeong,Do Youn Jun,Ghil Suk Yoon,Byung Woog Kang +10 more
TL;DR: In conclusion, PHGDH, PDK1, and PSAT were significantly increased in colonic TT compared with pNT, and the prognostic implication of these enzymes needs to be further investigated.