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Cytometry ; 41(4): 252-60, 2000 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-11084610

RESUMO

BACKGROUND: Cellular heterogeneity in drug response has important clinical implications, and is believed to develop over many generations during clonal evolution in human tumors. The purpose of this study was to determine the level of heterogeneity exhibited by sister cells soon after their birth. METHODS: Human ileocecal carcinoma cells (HCT-8) were followed up to 11 days in vitro after a 2-h exposure to 1 microM raltitrexed (IC(95)) in a time-lapse video system. RESULTS: Over five experiments, 414 cells were followed after exposure to raltitrexed. Immediate sterility occurred in 74% of treated cells. Only 6% of cells could produce more than two generations of offspring, and heterogeneity in drug response was seen. Comparing sister cells < 24 h old, the more proliferative sibling produced up to 73 times more offspring, with a median ratio of 9.0 (control median = 1.19). Offspring of prolific drug-treated cells had a decreased probability of division (68% compared with 92%) and an increased average interdivision time (19.0 h compared with 15.1 h). CONCLUSIONS: Short-term exposure to raltitrexed resulted in increased interdivision times and production of sterile offspring extending seven generations. Cellular heterogeneity (difference in proliferation potential comparing drug-treated sister cells) was evident without a period of clonal evolution.


Assuntos
Antimetabólitos Antineoplásicos/toxicidade , Neoplasias do Íleo/tratamento farmacológico , Neoplasias do Íleo/patologia , Microscopia de Vídeo/métodos , Quinazolinas/toxicidade , Tiofenos/toxicidade , Idoso , Divisão Celular/efeitos dos fármacos , Linhagem da Célula/efeitos dos fármacos , Células Clonais/citologia , Células Clonais/efeitos dos fármacos , Humanos , Masculino , Probabilidade , Células Tumorais Cultivadas
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