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A novel nano-immunoassay method for quantification of proteins from CD138-purified myeloma cells: biological and clinical utility

机译:一种从CD138纯化的骨髓瘤细胞中定量蛋白质的新型纳米免疫测定方法:生物学和临床应用

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摘要

Protein analysis in bone marrow samples from patients with multiple myeloma has been limited by the low concentration of proteins obtained after CD138+ cell selection. A novel approach based on capillary nano-immunoassay could make it possible to quantify dozens of proteins from each myeloma sample in an automated manner. Here we present a method for the accurate and robust quantification of the expression of multiple proteins extracted from CD138-purified multiple myeloma samples frozen in RLT Plus buffer, which is commonly used for nucleic acid preservation and isolation. Additionally, the biological and clinical value of this analysis for a panel of 12 proteins essential to the pathogenesis of multiple myeloma was evaluated in 63 patients with newly diagnosed multiple myeloma. The analysis of the prognostic impact of CRBN/Cereblon and IKZF1/Ikaros mRNA/protein showed that only the protein levels were able to predict progression-free survival of patients; mRNA levels were not associated with prognosis. Interestingly, high levels of Cereblon and Ikaros proteins were associated with longer progression-free survival only in patients who received immunomodulatory drugs and not in those treated with other drugs. In conclusion, the capillary nano-immunoassay platform provides a novel opportunity for automated quantification of the expression of more than 20 proteins in CD138+ primary multiple myeloma samples.
机译:多发性骨髓瘤患者骨髓样本中的蛋白质分析受到CD138 + 细胞选择后获得的蛋白质浓度低的限制。一种基于毛细管纳米免疫测定的新颖方法可以自动定量每个骨髓瘤样品中的数十种蛋白质。在这里,我们提出了一种准确,可靠地定量从冷冻在RLT Plus缓冲液中的CD138纯化的多发性骨髓瘤样品中提取的多种蛋白表达的方法,该方法通常用于核酸保存和分离。另外,在63例新诊断的多发性骨髓瘤患者中评估了该分析对多发性骨髓瘤发病机理必不可少的12种蛋白质的生物学和临床价值。对CRBN / Cereblon和IKZF1 / Ikaros mRNA /蛋白质的预后影响进行的分析表明,只有蛋白质水平才能预测患者的无进展生存期。 mRNA水平与预后无关。有趣的是,仅在接受免疫调节药物的患者而非其他药物治疗的患者中,高水平的Cereblon和Ikaros蛋白与更长的无进展生存期相关。总之,毛细管纳米免疫测定平台为自动定量CD138 + 多发性骨髓瘤样本中20多种蛋白的表达提供了新的机会。

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