Bioinspired imidazo[1,2-a:4,5-c′]dipyridines with dual antiproliferative and anti-migrative properties in human cancer cells: The SAR investigation

被引:6
作者
Alzain, Abdulrahim A. [1 ,2 ]
Brisson, Lucie [3 ]
Delaye, Pierre-Olivier [1 ]
Penichon, Melanie [1 ]
Chadet, Stephanie [4 ]
Besson, Pierre [4 ]
Chevalier, Stephan [3 ]
Allouchi, Hassan [1 ]
Mohamed, Magdi A. [5 ,6 ]
Roger, Sebastien [4 ,7 ]
Enguehard-Gueiffier, Cecile [1 ]
机构
[1] Univ Tours, Fac Pharm, EA 7502 SIMBA, 31 Ave Monge, F-37200 Tours, France
[2] Univ Gezira, Fac Pharm, Dept Pharmaceut Chem, POB 20, Gezira, Sudan
[3] Univ Tours, INSERM, UMR 1069 N2C, 10 Blvd Tonnelle, F-37032 Tours, France
[4] Univ Tours, EA 4245 T21, 10 Blvd Tonnelle, F-37032 Tours, France
[5] Univ Khartoum, Fac Pharm, Dept Pharmaceut Chem, Khartoum, Sudan
[6] Jouf Univ, Coll Pharm, Dept Pharmaceut Chem, Sakakah, Saudi Arabia
[7] Inst Univ France, F-75006 Paris, France
关键词
Imidazo[1,2-a:4,5-c ']dipyridines; Antiproliferative activity; Anti-migration activity; Harmine analogues; BETA-CARBOLINE; BIOLOGICAL EVALUATION; HARMINE; DERIVATIVES; ANTICANCER; ACID; HYBRIDS; DESIGN;
D O I
10.1016/j.ejmech.2021.113258
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Herein, we report the design, synthesis and evaluation of novel bioinspired imidazo[1,2- a:4,5c']dipyridines. The structural optimization identified four anti-proliferative compounds. Compounds 11, 18, 19 and 20 exhibited excellent anticancer activities in vitro with IC50 of 0.4-5 mu M against three human cancer cell lines (MDA-MB-468, MDA-MB-435s and MDA-MB-231). These four compounds induced apoptosis in MDA-MB-231 cells in a dose-dependent manner, targeting different apoptotic proteins expression: 11 increased the expression of pro-apoptotic Bax protein while 18-20 reduced the level of anti-apoptotic Bcl-2 protein. Compounds 18 and 19 also reduced MDA-MB-231 cells proliferation as measured by Ki67 staining. Furthermore, compounds were also tested for the ability to inhibit cell migration in the highly aggressive human MDA-MB-435s cell line. Six compounds of this series (8, 15, 18, 22, 23, 24) inhibited cell migration by 41-50% while four compounds (20, 25, 27, 30) inhibited the migration by 53-62% in wound-healing experiments. Interestingly, compound 20 presented both antiproliferative and anti-migration activities and might be a promising anti-metastatic agent for cancer treatment. (c) 2021 Elsevier Masson SAS. All rights reserved.
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页数:16
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