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一种临床相关的脉冲处理生成了一种硼替佐米耐药的骨髓瘤细胞系,该细胞系缺乏蛋白酶体突变,并且对 Bcl-2 抑制剂 venetoclax 敏感。

A clinically relevant pulse treatment generates a bortezomib-resistant myeloma cell line that lacks proteasome mutations and is sensitive to Bcl-2 inhibitor venetoclax.

机构信息

Department of Molecular and Systems Biology, and Norris Cotton Cancer Center, Geisel School of Medicine, Dartmouth College, Hanover, NH, USA.

SLDK-Rancho Biosciences, San Diego, CA, USA.

出版信息

Sci Rep. 2022 Jul 27;12(1):12788. doi: 10.1038/s41598-022-17239-3.

Abstract

Proteasome inhibitors bortezomib and carfilzomib are the backbones of treatments of multiple myeloma, which remains incurable despite many recent advances. With many patients relapsing despite high initial response rates to proteasome inhibitor-containing regimens, it is critical to understand the process of acquired resistance. In vitro generated resistant cell lines are important tools in this process. The majority of previously developed bortezomib-resistant cell lines bear mutations in the proteasome PSMB5 sites, the prime target of bortezomib and carfilzomib, which are rarely observed in patients. Here we present a novel bortezomib-resistant derivative of the KMS-12-BM multiple myeloma cell line, KMS-12-BM-BPR. Unlike previously published bortezomib-resistant cell lines, it was created using clinically relevant twice-weekly pulse treatments with bortezomib instead of continuous incubation. It does not contain mutations in the PSMB5 site and retains its sensitivity to carfilzomib. Reduced load on proteasome due to decreased protein synthesis appears to be the main cause of resistance. In addition, KMS-12-BM-BPR cells are more sensitive to Bcl-2 inhibitor venetoclax. Overall, this study demonstrates the feasibility of creating a proteasome inhibitor resistant myeloma cell lines by using clinically relevant pulse treatments and provides a novel model of acquired resistance.

摘要

蛋白酶体抑制剂硼替佐米和卡非佐米是多发性骨髓瘤治疗的骨干,尽管最近取得了许多进展,但这种疾病仍然无法治愈。尽管许多患者对包含蛋白酶体抑制剂的方案有很高的初始反应率,但仍会复发,因此了解获得性耐药的过程至关重要。体外产生的耐药细胞系是这一过程中的重要工具。以前开发的大多数硼替佐米耐药细胞系都在蛋白酶体 PSMB5 位点发生突变,这是硼替佐米和卡非佐米的主要靶点,而这些突变在患者中很少观察到。在这里,我们提出了一种新的硼替佐米耐药多发性骨髓瘤细胞系 KMS-12-BM 的衍生物,KMS-12-BM-BPR。与以前发表的硼替佐米耐药细胞系不同,它是使用临床相关的每周两次脉冲硼替佐米治疗而不是连续孵育产生的。它不包含 PSMB5 位点的突变,并保留对卡非佐米的敏感性。由于蛋白质合成减少导致的蛋白酶体负担减少似乎是耐药的主要原因。此外,KMS-12-BM-BPR 细胞对 Bcl-2 抑制剂 venetoclax 更敏感。总的来说,这项研究表明,通过使用临床相关的脉冲治疗来创建蛋白酶体抑制剂耐药的骨髓瘤细胞系是可行的,并提供了一种新的获得性耐药模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8608/9329464/59b00402f2ba/41598_2022_17239_Fig1_HTML.jpg

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