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Tetrandrine inhibits human brain glioblastoma multiforme GBM 8401 cancer cell migration and invasion in vitro.
Jiang, Yi-Wen; Cheng, Hsin-Yu; Kuo, Chao-Lin; Way, Tzong-Der; Lien, Jin-Cherng; Chueh, Fu-Shin; Lin, Yun-Lian; Chung, Jing-Gung.
Affiliation
  • Jiang YW; Department of Biological Science and Technology, China Medical University, Taichung, Taiwan.
  • Cheng HY; Department of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, China Medical University, Taichung, Taiwan.
  • Kuo CL; Department of Biological Science and Technology, China Medical University, Taichung, Taiwan.
  • Way TD; Department of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, China Medical University, Taichung, Taiwan.
  • Lien JC; Department of Chinese Pharmaceutical Sciences and Chinese Medicine Resources, China Medical University, Taichung, Taiwan.
  • Chueh FS; Department of Biological Science and Technology, China Medical University, Taichung, Taiwan.
  • Lin YL; School of pharmacy, China Medical University, Taichung, Taiwan.
  • Chung JG; Department of Food Nutrition and Health Biotechnology, Asia University, Wufeng, Taichung, Taiwan.
Environ Toxicol ; 34(4): 364-374, 2019 Apr.
Article in En | MEDLINE | ID: mdl-30549224
ABSTRACT
Tetrandrine (TET) has been reported to induce anti-cancer activity in many human cancer cells and also to inhibit cancer cell migration and invasion. However, there are no reports to show TET inhibits cell migration and invasion in human brain glioblastoma multiforme GBM 8401 cells. In this study, we investigated the anti-metastasis effects of TET on GBM 8401 cells in vitro. Under sub-lethal concentrations (from 1, 5 up to 10 µM), TET significantly inhibited cell mobility, migration and invasion of GBM 8401 cells that were assayed by wound healing and Transwell assays. Gelatin zymography assay showed that TET inhibited MMP-2 activity in GBM 8401 cells. Western blotting results indicated that TET inhibited several key metastasis-related proteins, such as p-EGFR(Tyr1068) , SOS-1, GRB2, Ras, p-AKT(Ser473) and p-AKT(Thr308) , NF-κB-p65, Snail, E-cadherin, N-cadherin, NF-κB, MMP-2 and MMP-9 that were significant reduction at 24 and 48 hours treatment by TET. TET reduced MAPK signaling associated proteins such as p-JNK1/2 and p-c-Jun in GBM 8401 cells. The electrophoretic mobility shift (EMSA) assay was used to investigate NF-κB and DNA binding was reduced by TET in a dose-dependently. Based on these findings, we suggested that TET could be used in anti-metastasis of human brain glioblastoma multiforme GBM 8401 cells in the future.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Cell Movement / Anticarcinogenic Agents / Glioblastoma / Benzylisoquinolines Limits: Humans Language: En Journal: Environ Toxicol Journal subject: SAUDE AMBIENTAL / TOXICOLOGIA Year: 2019 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Cell Movement / Anticarcinogenic Agents / Glioblastoma / Benzylisoquinolines Limits: Humans Language: En Journal: Environ Toxicol Journal subject: SAUDE AMBIENTAL / TOXICOLOGIA Year: 2019 Document type: Article Affiliation country: