Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2582762 | Environmental Toxicology and Pharmacology | 2016 | 9 Pages |
Abstract
This study is the first report of the antitumor activities of desmethylanhydroicaritin (DMAI) isolated from Sophora flavescens on U87MG cells. Human glioblastoma is one of the most aggressive malignant type of brain tumors and highly diffuses to around normal brain tissues. DMAI showed anti-proliferation effects on U87MG cells at the concentration of 30 μM, however did not affect to HEK-293 cells. DMAI induced anti-proliferation effects via ERK/MAPK, PI3 K/Akt/mTOR signal pathway and G2/M phase cell cycle arrest. DMAI led to morphological change and inhibition of filapodia formation through regulation of Rac 1 and Cdc 42. In addition, migration and invasion of U87MG cells were inhibited by DMAI via down-regulation of matrix metalloproteinase (MMP) â2 and MMP â9 expressions and activities. Our results suggest that DMAI has a potential as a therapeutic agent against glioblastoma cells.
Keywords
EGFRU87MGcdc2WST-1CDC42PARPDAPIERKmTORGAPDHPI3KMMPPBSBSAMAPKbovine serum albuminProliferationInvasioncell division cycle 2cell division cycle 42phosphoinositide 3-kinasematrix metalloproteinasePhosphate-buffered salineMigrationmammalian target of rapamycinmitogen activated protein kinasemitogen-activated protein kinasePoly(ADP-ribose) polymeraseextracellular receptor kinaseglyceraldehyde-3-phosphate dehydrogenaseEpidermal growth factor receptor
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Authors
Chang-Won Kang, Nan-Hee Kim, Huyn Ah Jung, Hyung-Wook Choi, Min-Jae Kang, Jae-Sue Choi, Gun-Do Kim,