
This study was aimed to explore the inhibitory effect of triptolide on proliferation and inducing apoptosis effect of K562/G01 cells and their possible mechanism. MTT assay was used to detect the effect of imatinib or triptolide alone and their combination on K562/G01 proliferation; the cell cycle, apoptosis rate, P-gp protein expression were detected by flow cytometry (FCM); the expression of P-gp was assessed by Western blot; the BCR/ABL gene expression was assayed by real time quantitative PCR. The results showed that triptolide could enhance the effect of imatinib on proliferation inhibition and apoptosis of K562/G01, arrested the cell cycle in G1 phase, down-regulated the expression of BCR/ABL gene and P-gp protein. It is concluded that triptolide induces K562/G01 cell proliferation inhibition and apoptosis, the mechanism may be related to cell cycle arrest, decrease of P-gp protein expression, inhibition of BCR/ABL gene expression.
ATP Binding Cassette Transporter, Subfamily B, Fusion Proteins, bcr-abl, Apoptosis, Cell Cycle Checkpoints, Phenanthrenes, Piperazines, Pyrimidines, Drug Resistance, Neoplasm, Benzamides, Imatinib Mesylate, Epoxy Compounds, Humans, ATP Binding Cassette Transporter, Subfamily B, Member 1, Diterpenes, K562 Cells, Cell Proliferation
ATP Binding Cassette Transporter, Subfamily B, Fusion Proteins, bcr-abl, Apoptosis, Cell Cycle Checkpoints, Phenanthrenes, Piperazines, Pyrimidines, Drug Resistance, Neoplasm, Benzamides, Imatinib Mesylate, Epoxy Compounds, Humans, ATP Binding Cassette Transporter, Subfamily B, Member 1, Diterpenes, K562 Cells, Cell Proliferation
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