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Effects of Artesunate Combined with Arsenious Acid on Proliferation and Apoptosis of Multiple Myeloma Cells via PI3K/AKT Signaling Pathway / 中国实验血液学杂志
Journal of Experimental Hematology ; (6): 1819-1824, 2021.
Article Dans Chinois | WPRIM | ID: wpr-922341
ABSTRACT
OBJECTIVE@#To investigate the effect of artesunate and arsenous acid and their combination on the proliferation and apoptosis of human multiple myeloma cells and their mechanism.@*METHODS@#Human multiple myeloma cell line RPMI 8226 cells were cultured and treated with 0, 1, 2, 4, 8 nmol/L arsenous acid and 0, 40, 80, 160, 320 μmol/L artesunate, respectively. The inhibition of cell growth was detected by CCK-8 assay. The apoptosis rate was detected by flow cytometry. QPCR was used to detect the mRNA expression of cell proliferation and apoptosis-related factors. The expression of cell proliferation, apoptosis-related factors and PI3K/AKT pathway protein were detected by Western blot.@*RESULTS@#CCK-8 assay showed that the growth of multiple myeloma cells was inhibited by arsenous acid and artesunate. The IC@*CONCLUSION@#Artesunate combined with arsenous acid inhibits proliferation and promotes apoptosis of tumor cells through PI3K/AKT signaling pathway, and is superior to the effect of two drugs alone.
Sujets)
Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Transduction du signal / Apoptose / Phosphatidylinositol 3-kinases / Lignée cellulaire tumorale / Facteur de croissance endothéliale vasculaire de type A / Prolifération cellulaire / Protéines proto-oncogènes c-akt / Artésunate / Myélome multiple Limites du sujet: Humains langue: Chinois Texte intégral: Journal of Experimental Hematology Année: 2021 Type: Article

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Texte intégral: Disponible Indice: WPRIM (Pacifique occidental) Sujet Principal: Transduction du signal / Apoptose / Phosphatidylinositol 3-kinases / Lignée cellulaire tumorale / Facteur de croissance endothéliale vasculaire de type A / Prolifération cellulaire / Protéines proto-oncogènes c-akt / Artésunate / Myélome multiple Limites du sujet: Humains langue: Chinois Texte intégral: Journal of Experimental Hematology Année: 2021 Type: Article