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Honokiol overcomes conventional drug resistance in human multiple myeloma by induction of caspase-dependent and -independent apoptosis

机译:厚朴酚通过诱导胱天蛋白酶依赖性和非依赖性凋亡来克服人多发性骨髓瘤的常规耐药性

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摘要

Honokiol (HNK) is an active component purified from magnolia, a plant used in traditional Chinese and Japanese medicine. Here we show that HNK significantly induces cytotoxicity in human multiple myeloma (MM) cell lines and tumor cells from patients with relapsed refractory MM. Neither coculture with bone marrow stromal cells nor cytokines (interleukin-6 and insulin-like growth factor-1) protect against HNK-induced cytotoxicity. Although activation of caspases 3, 7, 8, and 9 is triggered by HNK, the pan-caspase inhibitor z-VAD-fmk does not abrogate HNK-induced apoptosis. Importantly, release of an executioner of caspase-independent apoptosis, apoptosis-inducing factor (AIF), from mitochondria is induced by HNK treatment. HNK induces apoptosis in the SU-DHL4 cell line, which has low levels of caspase 3 and 8 associated with resistance to both conventional and novel drugs. These results suggest that HNK induces apoptosis via both caspase-dependent and -independent pathways. Furthermore, HNK enhances MM cell cytotoxicity and apoptosis induced by bortezomib. In addition to its direct cytotoxicity to MM cells, HNK also represses tube formation by endothelial cells, suggesting that HNK inhibits neovascurization in the bone marrow microenvironment. Taken together, our results provide the preclinical rationale for clinical protocols of HNK to improve patient outcome in MM. (Blood. 2005;106:1794-1800)
机译:厚朴酚(HNK)是从木兰中提取的活性成分,木兰是中药和日药中使用的植物。在这里,我们显示HNK会从难治性MM复发患者中诱导人多发性骨髓瘤(MM)细胞系和肿瘤细胞的细胞毒性。与骨髓基质细胞共培养或细胞因子(白介素6和胰岛素样生长因子1)都不能抵抗HNK诱导的细胞毒性。尽管胱天蛋白酶3、7、8和9的激活是由HNK触发的,但是泛半胱天冬酶抑制剂z-VAD-fmk不能消除HNK诱导的凋亡。重要的是,通过HNK处理诱导了从线粒体释放caspase非依赖性凋亡执行者,凋亡诱导因子(AIF)。 HNK在SU-DHL4细胞系中诱导凋亡,该细胞系具有低水平的caspase 3和8,与对常规药物和新药的耐药性相关。这些结果表明,HNK通过胱天蛋白酶依赖性和非依赖性途径诱导细胞凋亡。此外,HNK增强了硼替佐米诱导的MM细胞的细胞毒性和凋亡。 HNK除对MM细胞具有直接的细胞毒性外,还抑制内皮细胞的管形成,表明HNK抑制了骨髓微环境中的新血管硬化。综上所述,我们的结果为HNK改善MM患者预后的临床方案提供了临床前依据。 (2005年; 106:1794-1800)

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