Department of Medical Oncology, The LeBow Institute for Myeloma Therapeutics and Jerome Lipper Multiple Myeloma Center, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02115, USA.
Br J Haematol. 2010 May;149(4):537-49. doi: 10.1111/j.1365-2141.2010.08127.x. Epub 2010 Mar 12.
This study investigated the cytotoxicity and mechanism of action of AS703026, a novel, selective, orally bioavailable MEK1/2 inhibitor, in human multiple myeloma (MM). AS703026 inhibited growth and survival of MM cells and cytokine-induced osteoclast differentiation more potently (9- to 10-fold) than AZD6244. Inhibition of proliferation induced by AS703026 was mediated by G0-G1 cell cycle arrest and was accompanied by reduction of MAF oncogene expression. AS703026 further induced apoptosis via caspase 3 and Poly ADP ribose polymerase (PARP) cleavage in MM cells, both in the presence or absence of bone marrow stromal cells (BMSCs). Importantly, AS703026 sensitized MM cells to a broad spectrum of conventional (dexamethasone, melphalan), novel or emerging (lenalidomide, perifosine, bortezomib, rapamycin) anti-MM therapies. Significant tumour growth reduction in AS703026- vs. vehicle-treated mice bearing H929 MM xenograft tumours correlated with downregulated pERK1/2, induced PARP cleavage, and decreased microvessels in vivo. Moreover, AS703026 (<200 nmol/l) was cytotoxic against the majority of tumour cells tested from patients with relapsed and refractory MM (84%), regardless of mutational status of RAS and BRAF genes. Importantly, BMSC-induced viability of MM patient cells was similarly blocked within the same dose range. Our results therefore support clinical evaluation of AS703026, alone or in combination with other anti-MM agents, to improve patient outcome.
这项研究调查了 AS703026(一种新型、选择性、口服生物可利用的 MEK1/2 抑制剂)对人多发性骨髓瘤(MM)的细胞毒性和作用机制。AS703026 比 AZD6244 更有效地抑制 MM 细胞的生长和存活以及细胞因子诱导的破骨细胞分化(强 9-10 倍)。AS703026 诱导的增殖抑制是通过 G0-G1 细胞周期阻滞介导的,并伴随着 MAF 癌基因表达的减少。AS703026 通过半胱天冬酶 3 和多聚 ADP 核糖聚合酶(PARP)在 MM 细胞中的裂解进一步诱导细胞凋亡,无论骨髓基质细胞(BMSCs)是否存在。重要的是,AS703026 使 MM 细胞对广泛的传统(地塞米松、美法仑)、新型或新兴(来那度胺、培非司亭、硼替佐米、雷帕霉素)抗 MM 疗法敏感。AS703026 治疗组与对照组(vehicle)相比,携带 H929 MM 异种移植瘤的小鼠肿瘤生长明显减少,这与体内 pERK1/2 下调、PARP 裂解诱导和微血管减少有关。此外,AS703026(<200nmol/l)对大多数来自复发和难治性 MM 患者的肿瘤细胞具有细胞毒性(84%),而与 RAS 和 BRAF 基因的突变状态无关。重要的是,BMSC 诱导的 MM 患者细胞活力也在相同的剂量范围内被阻断。因此,我们的研究结果支持 AS703026 的临床评估,无论是单独使用还是与其他抗 MM 药物联合使用,以改善患者的预后。