Abstract | OBJECTIVE: To study the effect and mechanism of berbamine on the apoptosis of multidrug resistant leukemia K562/Adr cells and in reversing the drug resistance. METHODS: IC50 value of K562/Adr cell was determined with MTT method, cell apoptosis rate was analyzed by flow cytometry with Annexin V FITC-PI assay, with the peak and cell cycle detected by PI staining. At the same time, flow cytometry was also used in determining Caspase-3, P-GP protein expression and drug accumulating capacity in cells, and RT-PCR method was used to analyze the gene expression of mdr-1. RESULTS:
Berbamine could inhibit human leukemia K562/Adr cell growth in dose-dependent manner, it could also induce cell apoptosis, increase the protein expression of Caspase-3 and the drug excretion capacity of cells, reduce the mRNA and protein expression levels of mdr-1 gene. CONCLUSION:
Berbamine could activate Caspase-3 to induce human leukemia K562/Adr cell apoptosis, and by reducing mdr-1 gene expression to reverse its multidrug resistance.
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Authors | Qing-hua Dong, Shu Zheng, Rong-zhen Xu, Qinghua Lu, Liming He |
Journal | Zhongguo Zhong xi yi jie he za zhi Zhongguo Zhongxiyi jiehe zazhi = Chinese journal of integrated traditional and Western medicine
(Zhongguo Zhong Xi Yi Jie He Za Zhi)
Vol. 24
Issue 9
Pg. 820-2
(Sep 2004)
ISSN: 1003-5370 [Print] China |
PMID | 15495829
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- ATP Binding Cassette Transporter, Subfamily B, Member 1
- Alkaloids
- Antineoplastic Agents, Phytogenic
- Benzylisoquinolines
- RNA, Messenger
- CASP3 protein, human
- Caspase 3
- Caspases
- berbamine
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Topics |
- ATP Binding Cassette Transporter, Subfamily B, Member 1
(biosynthesis, genetics)
- Alkaloids
(pharmacology)
- Antineoplastic Agents, Phytogenic
(pharmacology)
- Apoptosis
(drug effects)
- Benzylisoquinolines
(pharmacology)
- Caspase 3
- Caspases
(biosynthesis, genetics)
- Drug Resistance, Neoplasm
(drug effects, genetics)
- Humans
- K562 Cells
- RNA, Messenger
(biosynthesis, genetics)
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