Identification of phenyl-pyridine-2-carboxylic acid derivatives as novel cell cycle inhibitors with increased selectivity for cancer cells

被引:4
作者
Berthel, SJ
Marks, IM
Yin, XF
Mischke, SG
Orzechowski, L
Pezzoni, G
Sala, F
Vassilev, LT
机构
[1] Hoffmann La Roche Inc, Roche Res Ctr, Discovery Oncol, Nutley, NJ 07110 USA
[2] Hoffmann La Roche Inc, Roche Res Ctr, Discovery Chem, Nutley, NJ 07110 USA
关键词
antitumor; cancer cells; cell cycle; mitosis; xenografts;
D O I
10.1097/00001813-200204000-00004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ro 41-4439, a phenyl-pyridine-2-carboxylic acid derivative, was identified by a cell-based screening approach that exploits the differences between normal and cancer cells in their sensitivity to cytotoxic agents. This compound showed low micromolar antiproliferative activity and cytotoxicity against a broad panel of human cancer cell lines in vitro, and over 10-fold selectivity to cancer cells when tested in parallel with a panel of proliferating normal human cells. Cytotoxicity of Ro 41-4439 is due to arrest of cell cycle progression in mitosis followed by induction of apoptosis. Four-week treatment of nude mice bearing established mammary tumor xenografts (MDA-MB-435) with well-tolerated doses of the compound showed 73% inhibition of tumor growth. Limited exploration of structure-activity relationships involving side chain length, and aryl and pyridine rings allowed for the identification of more potent analogs. [(C) 2002 Lippincott Williams Wilkins.].
引用
收藏
页码:359 / 366
页数:8
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