Schmidmaier Ralf, Simsek Meral, Baumann Philipp, Emmerich Bertold, Meinhardt Gerold
Department of Medicine Innenstadt, Division of Hematology and Oncology, University Hospital Munich, Munich, Germany.
Anticancer Drugs. 2006 Jul;17(6):621-9. doi: 10.1097/01.cad.0000215058.85813.02.
Despite advances in the treatment of multiple myeloma, it remains an incurable disease because of primary and secondary drug resistance. Mevalonate pathway inhibitors like bisphosphonates and statins have antimyeloma activity in vitro at very high concentrations, which may probably not be reached in vivo. NCI-H929, OPM-2, U266 and RPMI-8226 myeloma cell lines were treated in the presence or absence of bone marrow stromal cells with simvastatin or zoledronate in combination with classical antimyeloma drugs like melphalan or bortezomib. Zoledronate did not show substantial antimyeloma activity at low and intermediate concentrations, whereas simvastatin potently induced apoptosis in myeloma cells without signs of primary, cell-adhesion-mediated drug resistance. Furthermore, sequential blockage of the mevalonate pathway by zoledronate and simvastatin demonstrated synergistic induction of apoptosis and reversal of cell-adhesion-mediated drug resistance. Our data provide a rationale for combining zoledronate and simvastatin with classical antimyeloma drugs.
尽管在多发性骨髓瘤的治疗方面取得了进展,但由于原发性和继发性耐药性,它仍然是一种无法治愈的疾病。甲羟戊酸途径抑制剂如双膦酸盐和他汀类药物在体外极高浓度时具有抗骨髓瘤活性,而在体内可能无法达到这样的浓度。在有或没有骨髓基质细胞存在的情况下,用辛伐他汀或唑来膦酸联合美法仑或硼替佐米等经典抗骨髓瘤药物处理NCI-H929、OPM-2、U266和RPMI-8226骨髓瘤细胞系。唑来膦酸在低浓度和中等浓度时未显示出显著的抗骨髓瘤活性,而辛伐他汀能有效诱导骨髓瘤细胞凋亡,且没有原发性细胞黏附介导的耐药迹象。此外,唑来膦酸和辛伐他汀对甲羟戊酸途径的序贯阻断显示出协同诱导凋亡以及逆转细胞黏附介导的耐药性。我们的数据为将唑来膦酸和辛伐他汀与经典抗骨髓瘤药物联合使用提供了理论依据。