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Anticancer Drugs ; 5(1): 35-42, 1994 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-8186428

RESUMEN

The modulating effect of ethyldeshydroxy-sparsomycin (EDSM), an inhibitor of ribosomal protein synthesis, on cytostatic agents was studied on cultured B16 melanoma cells using the microculture tetrazolium test (MTT). The data were analyzed for true synergism using the combination index and the median effect principle. The extent of cytotoxic drug interaction was influenced by the duration of drug exposure, the dose ratio, as well as the treatment schedule. When drug ratios were used, synergism was observed upon pre- and post-treatment in combination with cisplatin, cytosine arabinoside (Ara-C), methotrexate (MTX) and 5-fluorouracil (5-FU). The combination of a fixed dose of EDSM was synergistic with cisplatin, Ara-C, vincristine (VCR) and MTX, in the order MTX > Ara-C > VCR > cisplatin, while the combinations with doxorubicin, 5-FU and etoposide (VP-16) were shown to be antagonistic. These results suggest that only certain drugs and treatment schedules might be worthwhile for combination studies with EDSM in vivo and indicate a role for EDSM as modifier of antitumor responses in cancer chemotherapy.


Asunto(s)
Antineoplásicos/farmacología , Esparsomicina/análogos & derivados , Animales , Antineoplásicos/antagonistas & inhibidores , Colorantes , Antagonismo de Drogas , Sinergismo Farmacológico , Melanoma Experimental/tratamiento farmacológico , Melanoma Experimental/fisiopatología , Ratones , Esparsomicina/antagonistas & inhibidores , Esparsomicina/farmacología , Sales de Tetrazolio , Tiazoles , Células Tumorales Cultivadas
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