Jin-Mu Yi
Chungbuk National University
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BMC Complementary and Alternative Medicine | 2012
Jin-Mu Yi; Jong-Shik Park; Se-Mi Oh; Jun Lee; Jinhee Kim; Dal-Seok Oh; Ok-Sun Bang; No Soo Kim
BackgroundGleditsia sinensis thorns have been widely used in traditional Korean medicine for the treatment of several diseases, including obesity, thrombosis, and tumor-related diseases. The aim of the study is to determine the antiangiogenic effect of Gleditsia sinensis thorns in vitro and in vivo in a bid to evaluate its potential as an anticancer drug.MethodsEthanol extract of Gleditsia sinensis thorns (EEGS) were prepared and used for in vitro and in vivo assays. In vitro antiangiogenic effect of EEGS was determined in HUVEC primary cells by cell migration and tube formation assays. In vivo antiangiogenic effect of EEGS was determined by measuring vessel formation and vascular endothelial cells migrating into the implanted matrigels in nude mice. The angiogenesis-related proteins of which expression levels were altered by EEGS were identified by proteomic analysis.ResultsEEGS exerted a dose-dependent antiproliferative effect on HUVEC cells without significant cytotoxicity. Angiogenic properties, such as cell migration and tube formation, were significantly inhibited by EEGS in a dose-dependent manner. New vessel formation was also suppressed by EEGS, as determined by the directed in vivo angiogenesis assays in nude mice. EEGS reduced the expression of proangiogenic proteins, endothelin 1 and matrix metallopeptidase 2, in HUVEC cells.ConclusionsOur findings suggest that EEGS can inhibit angiogenesis by down-regulating proangiogenic proteins, and therefore it should be considered as a potential anticancer drug targeting tumor-derived angiogenesis.
Journal of The Korean Society for Applied Biological Chemistry | 2012
Haejin Kim; Jin-Mu Yi; No Soo Kim; You Jin Lee; Jinhee Kim; Dal-Seok Oh; Se-Mi Oh; Ok-Sun Bang; Jun Lee
Activity-guided fractionation of an ethanol extract from the fruits of Vitex rotundifolia led to the isolation of three flavonoids (1–3), one lignan (4), and three phenolic compounds (5–7). The structures of compounds 1–7 were identified by NMR data. The efficacy of all compounds was evaluated by their cytotoxic activities against nine human cancer cell lines using an in vitro assay.
BMC Complementary and Alternative Medicine | 2015
Jin-Mu Yi; Ok-Sun Bang; No Soo Kim
BackgroundAngiogenesis is a general hallmark of cancer; therefore, the inhibition of tumor-derived angiogenesis is considered to be an attractive target in the development of anti-cancer agents. Sa-mi-yeon-geon-tang (SMYGT), a decoction that consists of four natural medicinal products, has been traditionally prescribed in Oriental medicine to treat diverse diseases, including cancer. In the present study, we investigated the anti-angiogenic potential of SMYGT in vitro and in ovo.MethodsThe anti-angiogenic potential of SMYGT was evaluated using conventional in vitro assays with human umbilical vein endothelial cells (HUVECs) and chorioallantoic membrane (CAM) assays with fertilized eggs. The expression changes of pro-angiogenic proteins and intracellular signaling in HUVECs following SMYGT treatment were determined by quantitative polymerase chain reaction, gelatinase zymography, and western blot analysis.ResultsSMYGT efficiently inhibited three-dimensional capillary-like tube formation by HUVECs on extracellular matrix supports, as well as new vessel formation on CAMs. SMYGT inhibited cell adhesion to the extracellular matrix and HUVEC cell invasion through Matrigel without affecting cell proliferation, viability, and motility. These anti-angiogenic effects of SMYGT in HUVECs were related to decreases in the phosphorylation of focal adhesion kinase and the expression of matrix metallopeptidase-2 activity.ConclusionsSMYGT exhibited an anti-angiogenic potential in both in vitro and in ovo experiments, which may partially contribute to its anti-tumor effect in clinical conditions. We suggest that SMYGT may be a promising source material for the development of anti-cancer chemotherapeutics that target angiogenesis.
BMC Complementary and Alternative Medicine | 2014
Jin-Mu Yi; Jong-Shik Park; Jun Kyoung Lee; Jin Tae Hong; Ok-Sun Bang; No Soo Kim
BackgroundAngiogenesis, which is initiated by certain tumor micro-environmental conditions and diverse protein factors, plays a pivotal role during tumor development and metastasis. Therefore, many efforts have been made to develop effective anti-angiogenic agents as anticancer therapeutics. In the current study, we investigated the anti-angiogenic potential of an ethanol extract of Annona atemoya seeds (EEAA) in vitro and in vivo.MethodsThe anti-angiogenic potential of EEAA was evaluated using various in vitro/in vivo models, including cell proliferation, migration, and tube formation by human umbilical vascular endothelial cells (HUVECs); a Matrigel plug assay; and tumor-induced angiogenesis. The expression of hypoxia-inducible factors (HIFs) and vascular endothelial growth factor (VEGF) was investigated using reverse transcription-polymerase chain reaction, immunoassays, and western blotting.ResultsEEAA was able to significantly inhibit the angiogenic properties of HUVECs in vitro as well as angiogenic factor-induced blood vessel formation in vivo. EEAA down-regulated the expression of VEGF and HIF-1alpha/2alpha at the mRNA and protein levels, respectively, in cancer cells under hypoxic conditions.ConclusionsEEAA shows a strong anti-angiogenic potential in both in vitro and in vivo systems, and we suggest that EEAA may be a valuable herbal source for anticancer drug development.
Archives of Pharmacal Research | 2013
You Jin Lee; No Soo Kim; Haejin Kim; Jin-Mu Yi; Se-Mi Oh; Ok-Sun Bang; Jun Lee
Oncology Letters | 2013
Se-Mi Oh; Jinhee Kim; Jun Lee; Jin-Mu Yi; Dal-Seok Oh; Ok-Sun Bang; No Soo Kim
Biological & Pharmaceutical Bulletin | 2014
Jun Lee; Jin-Mu Yi; Haejin Kim; You Jin Lee; Jong-Shik Park; Ok-Sun Bang; No Soo Kim
Biological & Pharmaceutical Bulletin | 2012
You Jin Lee; Jinhee Kim; Jin-Mu Yi; Se-Mi Oh; No Soo Kim; Haejin Kim; Dal-Seok Oh; Ok-Sun Bang; Jun Lee
Chemico-Biological Interactions | 2015
Ki Mo Kim; Deok Rim Heo; Jun Lee; Jong-Shik Park; Myung-Gi Baek; Jin-Mu Yi; Haejin Kim; Ok-Sun Bang
Biological & Pharmaceutical Bulletin | 2015
Jin-Mu Yi; Jinhee Kim; Jong-Shik Park; Jun Lee; You Jin Lee; Jin Tae Hong; Ok-Sun Bang; No Soo Kim