PaperPotentiation of etoposide cytotoxicity against a human ovarian cancer cell line by pretreatment with non-toxic concentrations of methotrexate or aphidicolin
References (15)
- et al.
Inhibition of protein synthesis reduces the cytotoxicity of 4′-(9-acridinylamino)methanesulfon-m-aniside without affecting DNA breakage and DNA topoisomerase II in a murine mastocytoma cell line
Biochem Pharmacol
(1989) - et al.
Increase in topoisomerase-II-mediated DNA breaks and cytotoxicity of VP16 in human U937 lymphoma cells pretreated with low doses of methotrexate
Int J Cancer
(1990) - et al.
Aphidicolin prevents mitotic cell division by interfering with the activity of DNA polymerase
Nature
(1978) - et al.
Mitozolomide activity on human cancer cells in vitro
Br J Cancer
(1986) - et al.
Synchronisation of cancer cell lines of human origin using methotrexate
Cytometry
(1990) - et al.
Effect of adriamycin on the cell cycle traverse and kinetics of cultured human lymphoblasts
Cancer Res
(1976) DNA as a target in cancer chemotherapy: Measurement of macromolecular DNA damage produced in mammalian cells by anticancer agents and carcinogens
There are more references available in the full text version of this article.
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