The antiproliferation effect of berbamine on k562 resistant cells by inhibiting NF-kappaB pathway.

• Abstract: Imatinib mesylate is effective against Ph chromosome-positive leukemia; however, resistance has been reported. High expression of bcr-abl in mRNA and protein levels, and other alterations were found in patients who experienced imatinib treatment failures and thus it is important to design alternative treatment strategies. The aim of this study was to evaluate the in vitro effect of berbamine, on imatinib-resistant chronic myelogenous leukemia (CML) K562 (K562-r) cells, and explore the mechanisms. The growth of K562-r cells was examined using the 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyl-tetrazolium bromide (MTT) assay. Morphological analysis and DNA agarose electrophoresis were used to detect apoptosis in K562-r cells, and the extent of the cells in the sub-G1 cell cycle phase was measured using flow cytometry. The expression levels of BCR-ABL, phospho-BCR-ABL, and nuclear factor kappaB (NF-kappaB), IkappaBalpha, phospho-IkappaBalpha, IkappaB kinases alpha(IKKalpha), and Survivin were determined by Western blot. bcr-abl mRNA expression was determined by RT-PCR. MTT assays indicated that berbamine significantly inhibited the proliferation of K562-r cells. Cells with characteristics of apoptosis were confirmed by morphology examination and DNA agarose electrophoresis and percentage of apoptosis were increased after treatment with berbamine. The results also showed that berbamine was able to down-regulate BCR-ABL and phospho-BCR-ABL proteins by affecting bcr-abl mRNA expression and decrease expression of nuclear NF-kappaB, phospho-IkappaBalpha, IKKalpha, and Survivin. Collectively, berbamine could inhibit the proliferation of K562-r cells and induce apoptosis. The mechanisms may be related at least in part, to inhibit BCR-ABL and its downstream NF-kappaB signaling. Berbamine may provide an alternative candidate for the treatment of patients with CML resistant to imatinib therapy.
• Authors: Yan-Lin Wei, Yun Liang, Lei Xu, Xiao-Ying Zhao (Affiliation: Department of Hematology, The Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou, Zhejiang Province, China.)
• Journal: Anatomical record (Hoboken, N.J. : 2007) (Anat Rec (Hoboken)) Vol. 292 Issue 7 Pg. 945-50 (Jul 2009) ISSN: 1932-8494 [Electronic] United States
• PMID: 19548306 (Publication Type: Evaluation Studies, Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• BIRC5 protein, human
• Benzylisoquinolines
• I-kappa B Proteins
• Indicators and Reagents
• Microtubule-Associated Proteins
• NF-kappa B
• Piperazines
• Pyrimidines
• RNA, Messenger
• Tetrazolium Salts
• NF-kappaB inhibitor alpha
• imatinib
• berbamine

Topics

• Antineoplastic Agents (pharmacology)
• Apoptosis (drug effects, physiology)
• Benzylisoquinolines (pharmacology)
• Cell Line, Tumor
• Cell Proliferation (drug effects)
• Down-Regulation (drug effects, physiology)
• Drug Evaluation, Preclinical (methods)
• Drug Resistance, Neoplasm (physiology)
• G1 Phase (drug effects, physiology)
• Genes, abl (drug effects, genetics)
• Humans
• I-kappa B Proteins (drug effects, metabolism)
• Indicators and Reagents
• K562 Cells
• Leukemia, Myelogenous, Chronic, BCR-ABL Positive (drug therapy, metabolism, physiopathology)
• Microtubule-Associated Proteins (drug effects, metabolism)
• NF-kappa B (antagonists & inhibitors, metabolism)
• Phosphorylation (drug effects)
• Piperazines (pharmacology)
• Pyrimidines (pharmacology)
• RNA, Messenger (drug effects, metabolism)
• Signal Transduction (drug effects, physiology)
• Tetrazolium Salts