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Vorinostat-induced bone loss might be related to drug toxicity

机译:vorinostat诱导的骨质损失可能与药物毒性有关

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摘要

There is growing evidence that some HDAC inhibitors, such as trichostatin A (TSA), valproic acid (VPA), and sodium butyrate (NaBu), which all belong to the "first generation" of HDACi, could stimulate os-teogenic differentiation of mesenchymal stem cells (MSCs) and exhibit anabolic effects on the skeleton [1-5]. However, McGee-Lawrence et al. demonstrated that another pan-inhibitor of class I and II HDAC proteins, Vorinostat (SAHA or Zolinza?), caused bone loss in C57BL/6J mice by inhibition of osteoblastogenic differentiation [6]. According to our own observations [7], we wish to give our opinion about this conclusion.
机译:越来越多的证据表明,一些HDAC抑制剂,如甲状腺炎素A(TSA),丙甲酸(VPA)和丁酸钠(NaBU),它们都属于HDACI的“第一代”,可以刺激间充质分化 干细胞(MSCs)并表现出骨骼骨骼的合成代谢效应[1-5]。 但是,McGee-Lawrence等人。 证明另一种泛抑制剂I类和II HDAC蛋白,vorinostat(Saha或Zolinza),通过抑制骨纤维素分化而导致C57BL / 6J小鼠中的骨质损失[6]。 根据我们自己的观察[7],我们希望促进我们对此结论的看法。

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