Pharmacological Rac1 inhibitors with selective apoptotic activity in human acute leukemic cell lines

被引:24
作者
Cabrera, Maia [1 ]
Echeverria, Emiliana [1 ]
Remes Lenicov, Federico [2 ]
Cardama, Georgina [3 ]
Gonzalez, Nazareno [3 ]
Davio, Carlos [1 ]
Fernandez, Natalia [1 ]
Lorenzano Menna, Pablo [3 ]
机构
[1] UBA, CONICET, Fac Farm & Bioquim, Inst Invest Farmacol,ININFA, Buenos Aires, DF, Argentina
[2] UBA, CONICET, Fac Med, Inst Invest Biomed Retrovirus & SIDA,INBIRS, Buenos Aires, DF, Argentina
[3] Univ Nacl Quilmes, Lab Oncol Mol, Buenos Aires, DF, Argentina
关键词
Rac1; acute myeloid leukemia; apoptosis; ZINC69391; 1A-116; NF-KAPPA-B; ACUTE LYMPHOBLASTIC-LEUKEMIA; GUANOSINE TRIPHOSPHATASES REPRESENT; ACUTE MYELOID-LEUKEMIA; HEMATOPOIETIC-CELL; RHO GTPASES; STEM-CELLS; CANCER; BCL-2; ACTIVATION;
D O I
10.18632/oncotarget.21533
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Rac1 GTPase has long been recognized as a critical regulatory protein in different cellular and molecular processes involved in cancer progression, including acute myeloid leukemia. Here we show the antitumoral activity of ZINC69391 and 1A-116, two chemically-related Rac1 pharmacological inhibitors, on a panel of four leukemic cell lines representing different levels of maturation. Importantly, we show that the main mechanism involved in the antitumoral effect triggered by the Rac1 inhibitors comprises the induction of the mitochondrial or intrinsic apoptotic pathway. Interestingly, Rac1 inhibition selectively induced apoptosis on patient-derived leukemia cells but not on normal mononuclear cells. These results show the potential therapeutic benefits of targeting Rac1 pathway in hematopoietic malignancies.
引用
收藏
页码:98509 / 98523
页数:15
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