POTENTIATION OF CYTOTOXICITY OF MITOMYCIN-C BY A POLYACETYLENIC ALCOHOL, PANAXYTRIOL

Citation
H. Matsunaga et al., POTENTIATION OF CYTOTOXICITY OF MITOMYCIN-C BY A POLYACETYLENIC ALCOHOL, PANAXYTRIOL, Cancer chemotherapy and pharmacology, 33(4), 1994, pp. 291-297
Citations number
27
Categorie Soggetti
Pharmacology & Pharmacy",Oncology
ISSN journal
03445704
Volume
33
Issue
4
Year of publication
1994
Pages
291 - 297
Database
ISI
SICI code
0344-5704(1994)33:4<291:POCOMB>2.0.ZU;2-G
Abstract
Polyacetylenic alcohol, panaxytriol, which was isolated from Panax gin seng C. A. Meyer, has antiproliferative activity against several kinds of tumor cells. In this paper, die effect of panaxytriol on the cytot oxicity of mitomycin C (MMC) against a human gastric carcinoma cell li ne, MK-1, was investigated. The combination of a subthreshold concentr ation of MMC and panaxytriol produced a significant cytotoxic effect, which indicates that the effects of panaxytriol and MMC are synergisti c. A synergistic effect was observed when MK-1 cells were treated with the mixture of MMC and panaxytriol or treated with MMC followed by pa naxytriol. In contrast, when MK-1 cells were exposed to panaxytriol an d then to MMC, only an additive effect was induced. With the aim of fi nding a possible mechanism, the effect of panaxytriol on the accumulat ion of MMC into the MK-1 cells was examined. Cellular concentrations o f MMC were measured by high-performance liquid chromatography (HPLC). When MK-1 cells were treated with a mixture of panaxytriol and MMC or first with MMC and then with panaxytriol, the cellular level of MMC wa s significantly higher than that in MK-1 cells treated with MMC alone, but no significantly increased accumulation was found when MK-1 cells were treated with panaxytriol followed by MMC. These results suggest that synergistic effects of panaxytriol and MMC may be induced by acce leration of the effect of MMC on cellular accumulation by panaxytriol. In addition, they suggest that the enhanced accumulation of MMC in MK -1 cells treated with panaxytriol can probably be attributed to the de creased fluidity of the cell membrane caused by panaxytriol.