S
Soo-Jin Jeong
Researcher at Kyung Hee University
Publications - 119
Citations - 2556
Soo-Jin Jeong is an academic researcher from Kyung Hee University. The author has contributed to research in topics: Apoptosis & Tumor necrosis factor alpha. The author has an hindex of 29, co-authored 118 publications receiving 2113 citations.
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Journal ArticleDOI
Melatonin synergistically enhances cisplatin‐induced apoptosis via the dephosphorylation of ERK/p90 ribosomal S6 kinase/heat shock protein 27 in SK‐OV‐3 cells
TL;DR: It is demonstrated that melatonin enhances cisplatin‐induced apoptosis via the inactivation of ERK/p90RSK/HSP27 cascade in SK‐OV‐3 cells as a potent synergist to cisPlatin treatment.
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Suppression of STAT3 and HIF-1 alpha mediates anti-angiogenic activity of betulinic acid in hypoxic PC-3 prostate cancer cells.
Jimin Shin,Hyo-Jeong Lee,Deok-Beom Jung,Ji Hoon Jung,Hyo-Jung Lee,Eun-Ok Lee,Seok-Geun Lee,Beom Sang Shim,Seung-Hoon Choi,Seong-Gyu Ko,Kwang Seok Ahn,Soo-Jin Jeong,Sung-Hoon Kim +12 more
TL;DR: It is suggested that betulinic acid has anti-angiogenic activity by disturbing the binding of HIF-1α and STAT3 to the VEGF promoter in hypoxic PC-3 cells.
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Sphingosine kinase 1 pathway is involved in melatonin-induced HIF-1α inactivation in hypoxic PC-3 prostate cancer cells.
Sung-Yun Cho,Hyo-Jeong Lee,Soo-Jin Jeong,Hyo-Jung Lee,Hyun-Seok Kim,Chang Yan Chen,Eun-Ok Lee,Sung-Hoon Kim +7 more
TL;DR: Melatonin suppresses HIF‐1α accumulation via inhibition of SPHK1 pathway and ROS generation in PC‐3 cells under hypoxia, and reactive oxygen species (ROS) scavenger N‐acteylcysteine enhanced melatonin‐inhibited HIF-1α expression and SPHK 1 activity.
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Anethole exerts antimetatstaic activity via inhibition of matrix metalloproteinase 2/9 and AKT/mitogen-activated kinase/nuclear factor kappa B signaling pathways.
Eun Jeong Choo,Yun-Hee Rhee,Soo-Jin Jeong,Hyo-Jung Lee,Hyun-Seok Kim,Hyun Suk Ko,Ji-Hyun Kim,Tae-Rin Kwon,Ji Hoon Jung,Jin-Hyoung Kim,Hyo-Jeong Lee,Eun-Ok Lee,Dae Keun Kim,Chang-Yan Chen,Sung-Hoon Kim +14 more
TL;DR: Findings indicate that anethole is a potent anti-metastatic drug that functions through inhibiting MMP-2/9 and AKT/mitogen-activated protein kinase (MAPK)/NF-κB signal transducers.
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Tanshinone IIA induces autophagic cell death via activation of AMPK and ERK and inhibition of mTOR and p70 S6K in KBM-5 leukemia cells.
TL;DR: It is suggested that Tan IIA induces autophagic cell death via activation of AMPK and ERK and inhibition of mTOR and p70 S6K in KBM‐5 cells as a potent natural compound for leukemia treatment.