Abstract |
Expression of the heat-shock protein HSP-60 is associated with poor survival in patients with ovarian carcinoma. We examined both the nature of the interaction between hyperthermia and cisplatin (DDP) using the human ovarian carcinoma cell line 2008 and the effect on this interaction of the induction of the heat-shock response. The nature of the interaction was assessed using median-effect analysis. Despite the observation that 45 degrees C hyperthermia increased the intracellular uptake of the DDP analog [3H]- cis-dichloro(ethylenediamine)platinum(II) ( DEP) during a 1-h exposure by 155% +/- 55% (P = 0.02), median-effect analysis indicated only cytotoxic additivity (combination index at the level of 50% cell kill, 0.96 +/- 0.25). When cells were first exposed to hyperthermia for various periods and then allowed to incubate at 37 degrees C for 4 h to allow induction of the heat-shock genes before being treated with DDP for 1 h, there was a very small degree of antagonism between hyperthermia and DDP (combination index at 50% cell kill, 1.11 +/- 0.04). Our results indicate that DDP and hyperthermia interact only in an additive manner against this human ovarian carcinoma cell line and that the induction of heat-shock proteins by hyperthermia does not significantly antagonize the activity of DDP.
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Authors | E Kimura, S B Howell |
Journal | Cancer chemotherapy and pharmacology
(Cancer Chemother Pharmacol)
Vol. 32
Issue 6
Pg. 419-24
( 1993)
ISSN: 0344-5704 [Print] Germany |
PMID | 7903066
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Chaperonin 60
- Heat-Shock Proteins
- Organoplatinum Compounds
- platinum ethylenediamine dichloride
- Cisplatin
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Topics |
- Cell Survival
(drug effects, physiology)
- Chaperonin 60
- Cisplatin
(pharmacology, therapeutic use)
- Combined Modality Therapy
- Cystadenocarcinoma, Serous
(metabolism, therapy)
- Female
- Gene Expression Regulation, Neoplastic
(physiology)
- Heat-Shock Proteins
(biosynthesis)
- Humans
- Hyperthermia, Induced
- Organoplatinum Compounds
(metabolism)
- Ovarian Neoplasms
(metabolism, therapy)
- Time Factors
- Tumor Cells, Cultured
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