Chauhan Dharminder, Li Guilan, Podar Klaus, Hideshima Teru, Mitsiades Constantine, Schlossman Robert, Munshi Nikhil, Richardson Paul, Cotter Finbarr E, Anderson Kenneth C
Dana-Farber Cancer Institute, 44 Binney St, Boston, MA 02215, USA.
Blood. 2004 Oct 15;104(8):2458-66. doi: 10.1182/blood-2004-02-0547. Epub 2004 Jun 24.
Bortezomib (PS-341), a selective inhibitor of proteasomes, induces apoptosis in multiple myeloma (MM) cells; however, prolonged drug exposure may result in cumulative toxicity and the development of chemoresistance. Here we show that combining PK-11195 (PK), an antagonist to mitochondrial peripheral benzodiazepine receptors (PBRs), with bortezomib triggers synergistic anti-MM activity even in doxorubicin-, melphalan-, thalidomide-, dexamethasone-, and bortezomib-resistant MM cells. No significant cytotoxicity was noted in normal lymphocytes. Low-dose combined PK and bortezomib treatment overcomes the growth, survival, and drug resistance conferred by interleukin-6 or insulin growth factor within the MM bone marrow milieu. The mechanism of PK + bortezomib-induced apoptosis includes: loss of mitochondrial membrane potential; superoxide generation; release of mitochondrial proteins cytochrome-c (cyto-c) and Smac; and activation of caspases-8/-9/-3. Furthermore, PK + bortezomib activates c-Jun NH2 terminal kinase (JNK), which translocates to mitochondria, thereby facilitating release of cyto-c and Smac from mitochondria to cytosol. Blocking JNK, by either dominant-negative mutant (DN-JNK) or cotreatment with a specific JNK inhibitor SP600125, abrogates both PK + bortezomib-induced release of cyto-c/Smac and induction of apoptosis. Together, these preclinical studies suggest that combining bortezomib with PK may enhance its clinical efficacy, reduce attendant toxicity, and overcome conventional and bortezomib resistance in patients with relapsed refractory MM.
硼替佐米(PS - 341)是一种蛋白酶体的选择性抑制剂,可诱导多发性骨髓瘤(MM)细胞凋亡;然而,长时间药物暴露可能导致累积毒性和化疗耐药性的产生。在此我们发现,将线粒体外周苯二氮䓬受体(PBR)拮抗剂PK - 11195(PK)与硼替佐米联合使用,即使在对阿霉素、美法仑、沙利度胺、地塞米松和硼替佐米耐药的MM细胞中也能引发协同抗MM活性。在正常淋巴细胞中未观察到明显的细胞毒性。低剂量联合使用PK和硼替佐米治疗可克服MM骨髓微环境中白细胞介素 - 6或胰岛素生长因子赋予的生长、存活和耐药性。PK +硼替佐米诱导凋亡的机制包括:线粒体膜电位丧失;超氧化物生成;线粒体蛋白细胞色素c(cyto - c)和Smac释放;以及半胱天冬酶 - 8/-9/-3的激活。此外,PK +硼替佐米激活c - Jun氨基末端激酶(JNK),其转位至线粒体,从而促进cyto - c和Smac从线粒体释放到细胞质中。通过显性负性突变体(DN - JNK)或与特异性JNK抑制剂SP600125共同处理来阻断JNK,可消除PK +硼替佐米诱导的cyto - c/Smac释放和凋亡诱导。总之,这些临床前研究表明,将硼替佐米与PK联合使用可能会提高其临床疗效,降低伴随的毒性,并克服复发难治性MM患者的传统耐药和硼替佐米耐药性。