Antiproliferative and pro-apoptotic activities of 2′- and 4′-aminochalcones against tumor canine cells

被引:36
|
作者
Santos, Mariana B. [1 ]
Pinhanelli, Vitor C. [2 ]
Garcia, Mayara A. R. [1 ]
Silva, Gabriel [2 ,3 ]
Baek, Seung J. [3 ]
Franca, Suzelei C. [2 ]
Fachin, Ana L. [2 ,4 ]
Marins, Mozart [2 ,4 ]
Regasini, Luis O. [1 ]
机构
[1] Sao Paulo State Univ Unesp, Inst Biosci Humanities & Exact Sci Ibilce, Dept Chem & Environm Sci, Campus Sao Jose Rio Preto, Sao Paulo, SP, Brazil
[2] Univ Ribeirao Preto, Biotechnol Unit, Ribeirao Preto, SP, Brazil
[3] Univ Tennessee, Coll Vet Med, Dept Biomed & Diagnost Sci, Knoxville, TN USA
[4] Univ Ribeirao Preto, Sch Med, Ribeirao Preto, SP, Brazil
基金
巴西圣保罗研究基金会;
关键词
Chalcone; Canine cancer; Antiproliferative; Apoptosis; HISTIOCYTIC SARCOMA; ANTICANCER ACTIVITY; TOPOISOMERASE-II; CHALCONES; DOGS; INHIBITORS; CANCER; FLAVONOIDS; NEOPLASIA; CCNU;
D O I
10.1016/j.ejmech.2017.06.049
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In the present study, a series of 2'- and 4'-aminochalcones were synthesized and their antiproliferative activity against a canine malignant histiocytic cell line (DH82) was evaluated. Particularly aminochalcones with a hydrophobic substituent on ring B proved to be potent antiproliferative agents. Among these compounds, aminochalcones 3, 4 and 11 inhibited the growth of DH82 cells, with IC50 values of 34.4, 31.4 and 38.2 mu M, respectively, and were three times more potent than etoposide (IC50 = 95.5 mu M). The selected chalcones induced death through apoptosis rather than necrosis in DH82 and non-tumorigenic Madin-Darby canine kidney cells (MDCK). Further experiments suggested that the aminochalcones interfere with the regulation of oncogenesitumor suppressor genes. Aminochalcone 11 inhibited transcription of the TOP011 alpha and TP53 genes and aminochalcone 4 down-regulated Sp1 protein expression in a concentration-dependent manner. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:884 / 889
页数:6
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