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Expression, mutation, and methylation of cereblon‐pathway genes at pre‐ and post‐lenalidomide treatment in multiple myeloma

机译:在多发性骨髓瘤中的邻邻邻邻邻邻邻三任业胺治疗中的遗传群基因的表达,突变和甲基化

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Cereblon (CRBN) is a target for immunomodulatory drugs. This study investigated the prognostic value of the expression of CRBN‐pathway genes on the clinical relevance of lenalidomide (Len) treatment and evaluated the levels of CRBN‐binding proteins and mutations in these genes after Len treatment. Forty‐eight primary multiple myeloma cells were collected prior to treatment with Len and dexamethasone (Ld) and 25 paired samples were obtained post‐Ld therapy. These tumor cells were used to determine the expression and mutated forms of the CRBN‐pathway genes. Following normalization with CRBN levels, there was a significantly reduced IKZF1/CRBN ratio in samples that responded poorly to Ld therapy. Moreover, patients with low ratios of IKZF1/CRBN showed a significantly shorter progression‐free survival (PFS) and overall survival (OS) than those with higher ratios. However, patients with high ratios of KPNA2/CRBN showed a significantly shorter PFS and OS than patients with lower ratios. Of the 25 paired samples analyzed, most samples showed a reduction in the expression of CRBN and an increase in IKZF1 gene expression. No mutations were observed in CRBN , IKZF1 , or CUL4A genes in the post‐Ld samples. In conclusion, a decreased expression of IKZF1 and increased expression of KPNA2 compared to that of CRBN mRNA predicts poor outcomes of Ld therapy.
机译:Cereblon(CRBN)是免疫调节药物的目标。本研究研究了CRBN-途径基因表达对LenAlidomide(Len)处理的临床相关性的预后值,并在LEN处理后评价这些基因中的CRBN结合蛋白和突变水平。在用LEN和地塞米松(LD)处理之前收集48个初级多发性骨髓瘤细胞,并获得了25个对疗法的成对样品。这些肿瘤细胞用于确定CRBN-途径基因的表达和突变形式。在用CRBN水平进行归一化后,样品中的IKZF1 / CRBN比率显着降低,响应于LD治疗差。此外,IKZF1 / CRBN比率低的患者显示出的无进展的存活率(PFS)和总存活率明显较短,而不是比具有更高比率的患者。然而,KPNA2 / CRBN比率高的患者显示出比较低比率较低的患者显着更短的PFS和OS。在分析的25个配对样品中,大多数样品显示CRBN表达和IKZF1基因表达的表达减少。在后LD样品中,在CRBN,IKZF1或CUL4A基因中观察到突变。总之,与CRBN mRNA相比,IKZF1的表达和KPNA2的表达增加预测LD治疗差的差。

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