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Anticancer Drugs ; 13(4): 359-66, 2002 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-11984081

RESUMO

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.


Assuntos
Antineoplásicos/farmacologia , Ácidos Carboxílicos/farmacologia , Ciclo Celular/efeitos dos fármacos , Neoplasias Mamárias Experimentais/tratamento farmacológico , Piridinas/farmacologia , Animais , Antineoplásicos/uso terapêutico , Apoptose/efeitos dos fármacos , Ácidos Carboxílicos/uso terapêutico , Sobrevivência Celular/efeitos dos fármacos , Avaliação Pré-Clínica de Medicamentos , Ensaios de Seleção de Medicamentos Antitumorais , Feminino , Humanos , Concentração Inibidora 50 , Camundongos , Camundongos Nus , Piridinas/uso terapêutico , Relação Estrutura-Atividade , Células Tumorais Cultivadas
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