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靶向多发性骨髓瘤治疗中的核输出蛋白。

Targeting Nuclear Export Proteins in Multiple Myeloma Therapy.

机构信息

Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, NY, USA.

Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, 1 Gustave L Levy Place, Box 1185, New York, NY, 10029, USA.

出版信息

Target Oncol. 2020 Dec;15(6):697-708. doi: 10.1007/s11523-020-00758-2.

Abstract

Multiple myeloma (MM) is an incurable malignancy of plasma cells with a clinical course characterized by multiple relapses and treatment refractoriness. While recent treatment advancements have extended overall survival (OS), refractory MM has a poor prognosis, with a median OS of between 4 and 6 months. Nuclear export inhibition, specifically inhibition of CRM1/XPO1, is an emerging novel treatment modality that has shown promise in treatment-refractory MM. Initially discovered in yeast in 1983, early clinical applications were met with significant toxicities that limited their utility. The creation of small molecule inhibitors of nuclear export (SINE) has improved on toxicity limitations and has led to investigation in a number of malignancies at the preclinical and clinical stages. Preclinical studies of SINEs in MM have shown that these molecules are cytotoxic to myeloma cells, play a role in therapy resensitization, and suggest a role in limiting bone disease progression. In July 2019, selinexor became the first nuclear export inhibitor approved for use in relapsed/refractory MM based on the STORM trial. As of May 2020, there were eight ongoing trials combining selinexor with standard treatment regimens in relapsed/refractory MM. Eltanexor, a second-generation SINE, is also under investigation and has shown preliminary signs of efficacy in an early clinical trial while potentially having an improved toxicity profile compared with selinexor. Results in ongoing trials will help further define the role of SINEs in MM.

摘要

多发性骨髓瘤(MM)是一种不可治愈的浆细胞恶性肿瘤,其临床病程的特点是多次复发和治疗耐药。虽然最近的治疗进展延长了总生存期(OS),但难治性 MM 的预后较差,中位 OS 为 4 至 6 个月。核输出抑制,特别是 CRM1/XPO1 的抑制,是一种新兴的治疗方法,在治疗耐药性 MM 方面显示出了希望。核输出抑制剂(SINE)于 1983 年在酵母中首次发现,早期的临床应用因毒性显著而受到限制,限制了其应用。小分子核输出抑制剂(SINE)的开发改善了毒性限制,并导致在临床前和临床阶段对多种恶性肿瘤进行了研究。SINE 在 MM 中的临床前研究表明,这些分子对骨髓瘤细胞具有细胞毒性,在治疗重敏化中发挥作用,并提示在限制骨病进展方面发挥作用。2019 年 7 月,selinexor 基于 STORM 试验成为首个获批用于复发性/难治性 MM 的核输出抑制剂。截至 2020 年 5 月,有八项正在进行的试验将 selinexor 与复发性/难治性 MM 的标准治疗方案联合使用。第二代 SINE 药物 eltanexor 也在研究中,在早期临床试验中显示出初步疗效,而与 selinexor 相比,其毒性谱可能有所改善。正在进行的试验结果将有助于进一步确定 SINE 在 MM 中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbf0/7570401/f291884232af/11523_2020_758_Fig1_HTML.jpg

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