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Establishment and Characteristics of a Novel Mantle Cell Lymphoma-derived Cell Line and a Bendamustine-resistant Subline

机译:新型套细胞淋巴瘤来源的细胞系和苯达莫司汀抗性亚系的建立和特性

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摘要

Background/Aim: Bendamustine hydrochloride (BH) is a key therapeutic agent for mantle cell lymphoma (MCL), while the mechanism underlying BH-resistance has not been verified. Materials and Methods: We compared molecular/biological characteristics of a newly-generated MCL-derived cell line KPUM-YY1 and its BH-resistant subline KPUM-YY1R. Results: The growth-inhibitory IC50 for BH was 20 μM in KPUM-YY1 cells, while cell proliferation was not inhibited by up to 60 μM BH in KPUM-YY1R cells. Compared to KPUM-YY1 cells, gene expression profiling in KPUM-YY1R cells revealed up-regulation of 312 genes, including ABCB1 encoding P-glycoprotein (P-gp), and microsomal glutathione S-transferase 1 (MGST1). Addition of either a P-gp inhibitor or a GST inhibitor, at least partly, restored sensitivity to BH in KPUM-YY1R cells. In addition, KPUM-YY1R cells showed cross-resistance against various anti-MCL chemotherapeutics. Conclusion: BH resistance is mediated by overlapping mechanisms with overexpression of ABCB1 and MGST1, and is potentially accompanied by multidrug resistance in MCL.
机译:背景/目的:盐酸苯达莫司汀(BH)是套细胞淋巴瘤(MCL)的关键治疗剂,但尚未证实其抗BH作用的机制。材料和方法:我们比较了新产生的MCL衍生细胞系KPUM-YY1及其抗BH的亚系KPUM-YY1R的分子/生物学特性。结果:在KPUM-YY1细胞中BH的生长抑制IC50为20μM,而在KPUM-YY1R细胞中高达60μMBH不能抑制细胞增殖。与KPUM-YY1细胞相比,KPUM-YY1R细胞中的基因表达谱揭示了312个基因的上调,包括编码P-糖蛋白(P-gp)的ABCB1和微粒体谷胱甘肽S-转移酶1(MGST1)。添加P-gp抑制剂或GST抑制剂至少部分恢复了KPUM-YY1R细胞对BH的敏感性。此外,KPUM-YY1R细胞对多种抗MCL化疗药物具有交叉耐药性。结论:BH耐药是由ABCB1和MGST1过表达的重叠机制介导的,并可能伴随MCL的多药耐药。

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