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Establishment and characterization of therapy-resistant mantle cell lymphoma cell lines derived from diff erent tissue sites

机译:来自不同组织部位的耐治疗套细胞淋巴瘤细胞系的建立和表征

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Mantle cell lymphoma (MCL) is a rare but aggressive form of B cell non-Hodgkin lymphoma in which therapy resistance is common. New therapeutic options have extended survival in refractory MCL but have not provided durable remission. Tools are needed to assess the molecular and genetic changes associated with therapy resistance. Therefore, therapy-resistant MCL cell lines were established from the liver, kidney and lungs of human Granta 519-bearing NOD-SCID (non-obese diabetic-severe combined immunodeficiency) mice following treatment with CHOP (cyclophosphamide, doxorubicin, vincristine, prednisone) chemotherapy in combination with bortezomib. The cytomorphologies, immunophenotypes, growth patterns in semi-solid agar, cytogenetic profiles and gene expression differences between these cell lines were characterized to identify major changes associated with therapy resistance. Therapy-resistant cell lines exhibit more aggressive growth patterns and markedly different gene expression profiles compared to parental Granta 519 cells. Thus, these stable therapy-resistant cell lines are useful models to further study the molecular basis of drug resistance and to identify clinically relevant molecular targets in MCL.
机译:套细胞淋巴瘤(MCL)是一种罕见但侵袭性的B细胞非霍奇金淋巴瘤,其中常见的治疗耐药性。新的治疗选择延长了难治性MCL的生存期,但未提供持久的缓解。需要工具来评估与治疗抗性相关的分子和遗传变化。因此,在用CHOP(环磷酰胺,阿霉素,长春新碱,泼尼松)治疗后,从人Granta 519携带性NOD-SCID(非肥胖-糖尿病-严重合并免疫缺陷)小鼠的肝,肾和肺中建立了抗药性的MCL细胞系。化疗与硼替佐米合用。这些细胞系之间的细胞形态,免疫表型,半固体琼脂中的生长方式,细胞遗传学特征和基因表达差异被表征为鉴定与治疗耐药性相关的主要变化。与亲本Granta 519细胞相比,抗治疗性细胞系表现出更具侵略性的生长模式和明显不同的基因表达谱。因此,这些稳定的对治疗有抗药性的细胞系是进一步研究药物抗性的分子基础并鉴定MCL中临床相关分子靶标的有用模型。

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