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骨髓瘤患者成骨细胞中Osterix的组成性下调:硼替佐米和来那度胺的体外作用

Constitutive down-regulation of Osterix in osteoblasts from myeloma patients: in vitro effect of Bortezomib and Lenalidomide.

作者信息

De Matteo Monica, Brunetti Anna Elisabetta, Maiorano Eugenio, Cafforio Paola, Dammacco Franco, Silvestris Franco

机构信息

DIMO, Department of Internal Medicine and Clinical Oncology, University of Bari Medical School, Piazza Giulio Cesare 11, 70124, Bari, Italy.

出版信息

Leuk Res. 2010 Feb;34(2):243-9. doi: 10.1016/j.leukres.2009.07.017. Epub 2009 Aug 4.

Abstract

Bortezomib and Lenalidomide have been shown to be effective in the control of multiple myeloma (MM) progression. We have investigated their role in the in vitro expression of Osterix by primary osteoblast cultures from MM patients and found that Osterix RNA was constitutively down-regulated in these cells. Treatment of osteoblasts with Bortezomib resulted in an increase of Osterix RNA and in enhanced activity of both BMP-2 and Runx2. Instead, Lenalidomide was unable to modify Osterix transcription. These findings provide additional evidence suggesting that, at least in vitro, Bortezomib promotes the osteoblast maturation whereas Lenalidomide is ineffective.

摘要

硼替佐米和来那度胺已被证明在控制多发性骨髓瘤(MM)进展方面有效。我们研究了它们在MM患者原代成骨细胞培养物中对骨形成蛋白(Osterix)体外表达的作用,发现这些细胞中Osterix RNA持续下调。用硼替佐米处理成骨细胞会导致Osterix RNA增加以及骨形态发生蛋白-2(BMP-2)和核心结合因子α1(Runx2)的活性增强。相反,来那度胺无法改变Osterix转录。这些发现提供了额外的证据表明,至少在体外,硼替佐米促进成骨细胞成熟而来那度胺无效。

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