来那度胺
硼替佐米
多发性骨髓瘤
医学
蛋白酶体抑制剂
小脑
沙利度胺
地塞米松
肿瘤科
内科学
药理学
癌症研究
化学
泛素
泛素连接酶
基因
生物化学
作者
Busong Wang,Jingjing Duan,Liang Zhou
出处
期刊:Anti-Cancer Drugs
[Ovid Technologies (Wolters Kluwer)]
日期:2021-03-01
卷期号:32 (3): 227-232
被引量:5
标识
DOI:10.1097/cad.0000000000001041
摘要
The combination of bortezomib (Velcade, PS-341) and lenalidomide (Revlimid) for the treatment of multiple myeloma was proved by USA Food and Drug Administration in 2006. Lenalidomide prevents the proliferation of multiple myeloma cells through binding to cereblon and promoting the ubiquitinational degradation of IKZF1 (Ikaros)/IKZF3 (Aiolos). However, the proteasome inhibitor bortezomib would inhibit the ubiquitinational degradation of IKZF1/IKZF3. How bortezomib could not block the antiproliferative effect of lenalidomide on multiple myeloma cells, which is the paradoxical pharmacological mechanisms in multiple myeloma. In this review, we summarized recent advances in molecular mechanisms underlying the combination of bortezomib and lenalidomide for the treatment multiple myeloma, discussed the paradoxical pharmacological mechanisms of lenalidomide and bortezomib in the treatment of multiple myeloma.
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