Zhu Kuichun, Gerbino Elvira, Beaupre Darrin M, Mackley Paul A, Muro-Cacho Carlos, Beam Craig, Hamilton Andrew D, Lichtenheld Mathias G, Kerr William G, Dalton William, Alsina Melissa, Sebti Saïd M
Drug Discovery Program, Biostatistics Core, H. Lee Moffitt Cancer Center & Research Institute, Tampa, FL 33612, USA.
Blood. 2005 Jun 15;105(12):4759-66. doi: 10.1182/blood-2004-11-4307. Epub 2005 Feb 22.
Despite major advances, multiple myeloma (MM) remains an incurable malignancy. Recently we have found that disease stabilization was achieved in 64% of patients with advanced MM treated with the farnesyltransferase inhibitor R115777 (Zarnestra) in a phase 2 clinical trial. In order to enhance R115777 antitumor activity in MM, we examined the combination of this novel agent with other anticancer drugs in MM cell lines. In this study, R115777 was found to synergize with paclitaxel and docetaxel, but not with other chemotherapy agents, including doxorubicin, 5-fluorouracil, cisplastin, melphalan, mitoxantrone, and dexamethasone. R115777 synergized with paclitaxel to inhibit MM cell proliferation and to induce apoptosis. Synergism in the induction of apoptosis was accompanied by increase in cytochrome c release and caspase-3 activation. Furthermore, flow cytometry analysis also showed that paclitaxel and R115777 synergized to induce G(2)/M cell-cycle arrest. Importantly, synergism was observed in taxane- and R115777-resistant MM cells. In the human severe combined immunodeficient (SCID-hu) bone model of myeloma growth, the ability of paclitaxel to inhibit tumor growth in vivo was enhanced by R115777. Combination of paclitaxel or docetaxel with R115777 in the treatment of MM cells from patients with multiple myeloma was more beneficial than treatment with single agents. Our results provide the basis for combination therapy clinical trials with paclitaxel or docetaxel with R115777 in MM patients.
尽管取得了重大进展,但多发性骨髓瘤(MM)仍然是一种无法治愈的恶性肿瘤。最近我们发现,在一项2期临床试验中,使用法尼基转移酶抑制剂R115777(Zarnestra)治疗的晚期MM患者中,64%实现了疾病稳定。为了增强R115777在MM中的抗肿瘤活性,我们在MM细胞系中研究了这种新型药物与其他抗癌药物的联合应用。在本研究中,发现R115777与紫杉醇和多西他赛协同作用,但与其他化疗药物(包括阿霉素、5-氟尿嘧啶、顺铂、美法仑、米托蒽醌和地塞米松)无协同作用。R115777与紫杉醇协同抑制MM细胞增殖并诱导凋亡。凋亡诱导中的协同作用伴随着细胞色素c释放增加和半胱天冬酶-3激活。此外,流式细胞术分析还表明,紫杉醇和R115777协同诱导G(2)/M期细胞周期阻滞。重要的是,在对紫杉烷和R115777耐药的MM细胞中也观察到了协同作用。在人类严重联合免疫缺陷(SCID-hu)骨髓瘤生长骨模型中,R115777增强了紫杉醇在体内抑制肿瘤生长的能力。紫杉醇或多西他赛与R115777联合治疗多发性骨髓瘤患者的MM细胞比单药治疗更有益。我们的结果为MM患者使用紫杉醇或多西他赛与R115777进行联合治疗临床试验提供了依据。