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J Recept Signal Transduct Res ; 40(6): 591-598, 2020 Dec.
Article in English | MEDLINE | ID: mdl-32496906

ABSTRACT

Tanshinone IIA (Tan IIA) is a member of the major lipophilic components extracted from the root of Salvia miltiorrhiza Bunge. Osteosarcomas are primary malignant tumors of bone. The aim of our study is to explore the role of Tan IIA in osteosarcomas survival, migration, and proliferation. MG63 osteosarcoma cell line was cultured in vitro and treated with different concentrations of Tan IIA. Then, ELISA, immunofluorescence, qPCR, western blots, and pathway analysis were conducted to verify whether Tan II modulated osteosarcoma survival, migration, and proliferation through the AMPK/Nrf2 signaling pathway. Our results indicated that Tan IIA dose-dependently inhibited MG63 osteosarcoma cell survival, migration, and proliferation. Mechanistically, Tan IIA reduced cell viability and inhibited the transcriptions of migratory factors. In addition, the number of proliferative MG63 osteosarcoma cell was also reduced by Tan IIA. Molecular investigations demonstrated that Tan IIA treatment caused a drop in the transcriptions and activities of AMPK and Nrf2. Interestingly, knockdown of AMPK and Nrf2 markedly attenuated MG63 osteosarcoma cell survival, migration, and proliferation. Altogether, our results indicate that Tan IIA could be used as an effective anticancer drug to control osteosarcoma proliferation through affecting its survival, migration, and proliferation.


Subject(s)
AMP-Activated Protein Kinases/metabolism , Abietanes/pharmacology , Biomarkers, Tumor/metabolism , Bone Neoplasms/drug therapy , Gene Expression Regulation, Neoplastic/drug effects , NF-E2-Related Factor 2/metabolism , Osteosarcoma/drug therapy , AMP-Activated Protein Kinases/genetics , Antineoplastic Agents, Phytogenic/pharmacology , Apoptosis , Biomarkers, Tumor/genetics , Bone Neoplasms/metabolism , Bone Neoplasms/pathology , Cell Proliferation , Humans , NF-E2-Related Factor 2/genetics , Osteosarcoma/metabolism , Osteosarcoma/pathology , Tumor Cells, Cultured
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