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Jun Hee Lim

Researcher at Ajou University

Publications -  6
Citations -  453

Jun Hee Lim is an academic researcher from Ajou University. The author has contributed to research in topics: Downregulation and upregulation & Unfolded protein response. The author has an hindex of 6, co-authored 6 publications receiving 408 citations. Previous affiliations of Jun Hee Lim include UPRRP College of Natural Sciences.

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Curcumin sensitizes tumor necrosis factor-related apoptosis-inducing ligand (TRAIL)-induced apoptosis through reactive oxygen species-mediated upregulation of death receptor 5 (DR5)

TL;DR: It is demonstrated that subtoxic concentrations of curcumin sensitize human renal cancer cells to the tumor necrosis factor-related apoptosis inducing ligand (TRAIL-mediated apoptosis) by ROS-mediated DR5 upregulation.
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Monensin, a polyether ionophore antibiotic, overcomes TRAIL resistance in glioma cells via endoplasmic reticulum stress, DR5 upregulation and c-FLIP downregulation

TL;DR: Monensin effectively sensitizes various glioma cells, but not normal astrocytes, to TRAIL-mediated apoptosis; this occurs at least partly via monensin-induced endoplasmic reticulum (ER) stress, CHOP-mediated DR5 upregulation and proteasome-mediated downregulation of c-FLIP.
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Resveratrol induces pro-apoptotic endoplasmic reticulum stress in human colon cancer cells.

TL;DR: Treatment of HT29 human colon carcinoma cells with resveratrol was found to induce a number of signature ER stress markers, and the inhibition of caspase-4 activity by z-LEVD-fmk significantly reduced resver atrol-induced apoptosis, providing strong evidence to support an important role of ER stress response in mediating the resverAtrol- induced apoptosis.
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Molecular cloning and characterization of the human budding uninhibited by benomyl (BUB3) promoter.

TL;DR: A series of studies designed to understand the genomic structure of BUB3, particularly as it relates to regulation of gene expression are described, indicating that this region 5' region contains distinctive positive and negative regulatory elements.
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Influence of p53 and p21Waf1 expression on G2/M phase arrest of colorectal carcinoma HCT116 cells to proteasome inhibitors

TL;DR: The release experiments from nocodazole-induced mitotic phase cells indicated that MG132 inhibits the proliferation of HCT116 cells via arrest in the G2 phase, suggesting that p53 and p21 may not be essential for MG132-induced G2/M phase arrest.