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Cancer Res ; 49(16): 4452-4, 1989 Aug 15.
Article in English | MEDLINE | ID: mdl-2501025

ABSTRACT

The induction of glucose-regulated proteins by a variety of specific inducers leads to an increase in resistance to Adriamycin (Shen et al., Proc. Natl., Acad. Sci. USA, 84: 3278, 1987). In this study we examine several additional agents for cross-resistance induced during a glucose-regulated response in an attempt to better define the mechanism through which this phenomenon occurs. When anoxia, calcium ionophore A23187, or 2-deoxyglucose are used, a substantial resistance is obtained against the topoisomerase II-targeted agent, etoposide. Partial resistance is induced against vincristine and actinomycin D. Glucose-regulated protein inducers do not substantially alter cellular response to either bleomycin or radiation. In the case of mitomycin C there is a cellular sensitization with anoxia and 2-deoxyglucose while calcium ionophore A23187 had no effect on survival. This study suggests that the resistance obtained during a glucose-regulated response against etoposide and Adriamycin may involve topoisomerase II.


Subject(s)
Etoposide/metabolism , HSP70 Heat-Shock Proteins , Membrane Proteins/biosynthesis , Ovarian Neoplasms/metabolism , Animals , Calcimycin/deficiency , Cricetinae , Cricetulus , Dactinomycin/metabolism , Deoxyglucose/deficiency , Doxorubicin/metabolism , Drug Resistance , Female , Hypoxia/metabolism , Tumor Cells, Cultured/metabolism , Vincristine/metabolism
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