慢性粒细胞白血病
K562细胞
细胞凋亡
断点群集区域
白血病
化学
伊马替尼
癌症研究
半胱氨酸蛋白酶
阿布勒
费城染色体
免疫学
生物
程序性细胞死亡
生物化学
信号转导
受体
髓系白血病
酪氨酸激酶
染色体易位
基因
作者
Romano Silvestri,Gabriella Marfè,M. Artico,Giuseppe La Regina,Antonio Lavecchia,Ettore Novellino,Manuela Morgante,Carla Di Stefano,Gianfranco Catalano,Giuseppe Filomeni,Elisabetta Abruzzese,Maria Rosa Ciriolo,Matteo Antonio Russo,Sergio Amadori,Roberto Cirilli,Francesco La Torre,Paola Sinibaldi Salimei
摘要
Pyrrolo[1,2-b][1,2,5]benzothiadiazepine 5,5-dioxides (PBTDs) induced apoptosis in human BCR-ABL-expressing leukemia cells. The apoptotic activity was also observed in primary leukemic blasts, obtained from chronic myelogenous leukemia (CML) patients at onset or from patients in blast crisis and who were imatinib-resistant. Compounds 5 and 14 induced apoptosis before BCR-ABL protein expression and tyrosin phosphorylation were affected and activated different caspases in the apoptotic pathway. PBTDs are a new class of valid candidates for the treatment of CML.
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