OTTO, AM (1994) COMBINATIONS OF INTERFERON WITH PLATINUM COMPLEXES - SYNERGISTIC AND ANTAGONISTIC EFFECTS ON GROWTH-INHIBITION OF MCF-7 AND MDA-MB(231) BREAST-CANCER CELLS. JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY, 120 (5). pp. 286-292. ISSN 0171-5216,
Full text not available from this repository.Abstract
The growth-inhibitory effects of combining interferons (IFN) with platinum(II) complexes were tested with the aim of comparing these in cultures of estrogen-receptor(ER)-negative MDA-MB(231) and ER-positive MCF-7 breast cancer cell lines. Another aim was to test whether IFN as a biological response modifier could enhance the effect of the Pt complexes in vitro in an attempt to find an explanation for their more potent antitumor effects in in vivo models. Here it is shown that in both cell lines the combinations of different IFN with all three Pt complexes generally resulted in additive growth inhibition, as calculated by the product of the fraction of surviving cells obtained with each compound alone. Moreover, in MCF-7 cells natural IFN beta (nIFN beta) combined with aqua[meso-1,2-bis-(2,6-dichloro-4-hydroxyphenyl)ethylenediamine]sulfatoplatinum(II) (meso-6-Pt) resulted in synergistic inhibition. This synergy could be attributed to the estrogenic property of meso-6-Pt, since the ligand and estradiol also enhanced the inhibitory effect of nIFN beta. In contrast, the combination of recombinant IFN gamma and meso-6-Pt was antagonistic in MDA-MB(231) cells. These results show that, in spite of the similar responses of the ER-negative and ER-positive cells to each compound alone, these cells show unexpected differences in their sensitivity to combinations of IFN and the new Pt complex meso-6-Pt.
| Item Type: | Article |
|---|---|
| Uncontrolled Keywords: | AGENTS; CYCLE; GAMMA; LINES; ALPHA; DISSOCIATION; TAMOXIFEN; PHASE; BETA; BREAST CANCER; INTERFERON; MCF-7; MDA-MB(231); PLATINUM COMPLEXES |
| Depositing User: | Dr. Gernot Deinzer |
| Last Modified: | 19 Oct 2022 08:40 |
| URI: | https://pred.uni-regensburg.de/id/eprint/53434 |
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