Antiproliferative activity of 2,3-disubstituted indoles toward apoptosis-resistant cancers cells

被引:11
作者
Magedov, Igor V. [1 ]
Lefranc, Florence [2 ]
Frolova, Liliya V. [1 ]
Banuls, Laetitia Moreno Y. [3 ]
Peretti, Amanda S. [4 ]
Rogelj, Snezna [4 ]
Mathieu, Veronique [3 ]
Kiss, Robert [3 ]
Kornienko, Alexander [5 ]
机构
[1] New Mexico Inst Min & Technol, Dept Chem, Socorro, NM 87801 USA
[2] Univ Libre Brussels, Hop Erasme, Serv Neurochirurg, B-1070 Brussels, Belgium
[3] ULB, Fac Pharm, Lab Toxicol, B-1050 Brussels, Belgium
[4] New Mexico Inst Min & Technol, Dept Biol, Socorro, NM 87801 USA
[5] Texas State Univ San Marcos, Dept Chem & Biochem, San Marcos, TX 78666 USA
关键词
Cancer; Apoptosis resistance; Indole; Antiproliferative; GLIOMA-CELLS; GLIOBLASTOMA; CHEMOTHERAPY; SURVIVAL; MODELS;
D O I
10.1016/j.bmcl.2013.03.110
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Many types of cancer, including glioma, melanoma, NSCLC, among others, are resistant to apoptosis induction and poorly responsive to current therapies with propaptotic agents. We describe a series of 2,3-disubstituted indoles, which display cytostatic rather than cytotoxic effects in cancer cells, and serve as a new chemical scaffold to develop anticancer agents capable of combating apoptosis-resistant cancers associated with dismal prognoses. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:3277 / 3282
页数:6
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