Hematopathology Unit, Department of Pathology, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Spain.
Blood. 2011 Jan 27;117(4):1270-9. doi: 10.1182/blood-2010-04-278853. Epub 2010 Nov 24.
Despite the promising introduction of the proteasome inhibitor bortezomib in the treatment of mantle cell lymphoma (MCL), not all patients respond, and resistance often appears after initial treatment. By analyzing a set of 18 MCL samples, including cell lines with constitutive or induced resistance to bortezomib, we found a high correlation between loss of sensitivity to the proteasome inhibitor and up-regulation of the prosurvival chaperone BiP/Grp78. BiP/Grp78 stabilization was ensured at a posttranscriptional level by an increase in the chaperoning activity of heat shock protein of 90 kDa (Hsp90). In bortezomib-resistant cells, both BiP/Grp78 knockdown and cell pretreatment with the Hsp90 inhibitor of the ansamycin class, IPI-504, led to synergistic induction of apoptotic cell death when combined with bortezomib. Cell exposure to the IPI-504-bortezomib combination provoked the dissociation of Hsp90/BiP complexes, leading to BiP/Grp78 depletion, inhibition of unfolded protein response, and promotion of NOXA-mediated mitochondrial depolarization. The IPI-504-bortezomib combination also prevented BiP/Grp78 accumulation, thereby promoting apoptosis and inhibiting the growth of bortezomib-resistant tumors in a mouse model of MCL xenotransplantation. These results suggest that targeting unfolded protein response activation by the inhibition of Hsp90 may be an attractive model for the design of a new bortezomib-based combination therapy for MCL.
尽管蛋白酶体抑制剂硼替佐米在治疗套细胞淋巴瘤(MCL)方面有很大的前景,但并非所有患者都有反应,而且在初始治疗后往往会出现耐药性。通过分析包括对硼替佐米具有固有或诱导耐药性的细胞系在内的 18 个 MCL 样本,我们发现对蛋白酶体抑制剂的敏感性丧失与生存促进伴侣蛋白 BiP/Grp78 的上调之间存在高度相关性。BiP/Grp78 的稳定是通过热休克蛋白 90 kDa(Hsp90)的伴侣活性增加在转录后水平得到保证的。在硼替佐米耐药细胞中,BiP/Grp78 的敲低以及用安莎霉素类 Hsp90 抑制剂 IPI-504 预处理细胞,当与硼替佐米联合使用时,可协同诱导细胞凋亡。细胞暴露于 IPI-504-硼替佐米联合用药中会引发 Hsp90/BiP 复合物的解离,导致 BiP/Grp78 耗竭,抑制未折叠蛋白反应,并促进 NOXA 介导的线粒体去极化。IPI-504-硼替佐米联合用药还可防止 BiP/Grp78 的积累,从而促进凋亡并抑制 MCL 异种移植小鼠模型中硼替佐米耐药肿瘤的生长。这些结果表明,通过抑制 Hsp90 来靶向未折叠蛋白反应的激活可能是设计新的基于硼替佐米的联合治疗 MCL 的有吸引力的模型。