...
首页> 外文期刊>Blood: The Journal of the American Society of Hematology >The novel mechanism of lenalidomide activity
【24h】

The novel mechanism of lenalidomide activity

机译:来那度胺活性的新机制

获取原文
获取原文并翻译 | 示例

摘要

Lenalidomide acts by a novel drug mechanism-modulation of the substrate specificity of the CRL4(CRBN) E3 ubiquitin ligase. In multiple myeloma, lenalidomide induces the ubiquitination of IKZF1 and IKZF3 by CRL4 CRBN. Subsequent proteasomal degradation of these transcription factors kills multiple myeloma cells. In del(5q) myelodysplastic syndrome, lenalidomide induces the degradation of CK1a, which preferentially affects del(5q) cells because they express this gene at haploinsufficient levels. In the future, modulation of ubiquitin ligase function may enable us to target previously "undruggable" proteins.
机译:来那度胺的作用是通过新型药物机制调节CRL4(CRBN)E3泛素连接酶的底物特异性。在多发性骨髓瘤中,来那度胺通过CRL4 CRBN诱导IKZF1和IKZF3泛素化。这些转录因子随后的蛋白酶体降解会杀死多发性骨髓瘤细胞。在del(5q)骨髓增生异常综合症中,来那度胺会诱导CK1a降解,这会优先影响del(5q)细胞,因为它们以单倍不足的水平表达该基因。将来,对泛素连接酶功能的调节可能使我们能够靶向以前“不可吸收的”蛋白质。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号