Department of Medical Oncology, Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA 02215, USA.
Br J Haematol. 2012 Nov;159(3):340-51. doi: 10.1111/j.1365-2141.2012.09253.x. Epub 2012 Sep 13.
Jasmonates, plant stress hormones, have been demonstrated to be effective in killing various types of cancer cells. We therefore tested if methyljasmonate (MJ) has activity against multiple myeloma (MM) in vitro and in vivo. MM cell lines and primary MM tumour cells responded to MJ in vitro at concentrations that did not significantly affect normal haematopoietic cells, without stroma-mediated resistance. Brief MJ exposures of MM cells caused release of Hexokinase 2 (HK2) from mitochondria, rapid ATP depletion, perturbation of major intracellular signalling pathways, and ensuing mainly apoptotic cell death. Sensitivity to MJ correlated with lower cellular glucose consumption and lactate production, as well as lower intracellular protein levels of HK2, phosphorylated Voltage-dependent anion channel 2/3 (pVDAC2/3) and Aldo-keto reductase family 1 member C1 (AKR1C1), which represent potential biomarkers of responsiveness to MJ treatment, especially as AKR1C1 transcript levels also correlate with clinical outcome in bortezomib- or dexamethasone-treated MM patients. Interestingly, MJ synergized with bortezomib in vitro and prolonged survival of immunocompromised mice harbouring diffuse lesions of MM.1S cells compared to vehicle-treated mice (P = 0·0046). These studies indicate that jasmonates represent a new, promising strategy to treat MM.
茉莉酸,植物应激激素,已被证实对多种类型的癌细胞具有杀伤作用。因此,我们测试了茉莉酸甲酯(MJ)在体外和体内对多发性骨髓瘤(MM)是否具有活性。MM 细胞系和原代 MM 肿瘤细胞在体外对 MJ 有反应,浓度不会显著影响正常造血细胞,也没有基质介导的耐药性。MM 细胞的短暂 MJ 暴露会导致己糖激酶 2(HK2)从线粒体中释放,导致 ATP 迅速耗竭,主要细胞内信号通路受到干扰,随后主要发生细胞凋亡。对 MJ 的敏感性与细胞葡萄糖消耗和乳酸生成减少以及 HK2、磷酸化电压依赖性阴离子通道 2/3(pVDAC2/3)和醛酮还原酶家族 1 成员 C1(AKR1C1)的细胞内蛋白水平降低有关,这代表了对 MJ 治疗反应的潜在生物标志物,尤其是 AKR1C1 转录水平也与硼替佐米或地塞米松治疗的 MM 患者的临床结果相关。有趣的是,MJ 在体外与硼替佐米协同作用,并延长了携带 MM.1S 细胞弥漫性病变的免疫缺陷小鼠的存活时间,与接受载体治疗的小鼠相比(P=0.0046)。这些研究表明,茉莉酸盐代表了治疗 MM 的一种新的、有前途的策略。