| Literature DB >> 10601799 |
T W Leung1, G Cheng, C H Chui, S K Ho, F Y Lau, J K Tjong, T C Poon, J C Tang, W C Tse, K F Cheng, Y C Kong.
Abstract
Yuehchukene (YCK) is a novel bis-indole alkaloid with weak estrogenic activity. Biochemical studies showed that YCK could attenuate estrogenic action. In this study, the response of MCF-7, an estrogen-receptor-positive breast cancer cell line, under different combinations of estradiol, cyclophosphamide and YCK, was tested. From the dose-response curve, we discovered that 10(-2) M cyclophosphamide, even in its so-called 'bio-inert' form, could inhibit MCF-7 cell growth. However, the cytotoxic effect of cyclophosphamide was lost by reducing its concentration to approximately 1 x 10(-3) M. On the other hand, a low concentration ( approximately 10(-8)-10(-9) M) of YCK was found to potentiate the cytotoxic effect of cyclophosphamide on the MCF-7 cell line. Such an effect was absent in the estrogen-receptor-negative cell line MDA-MB-231. These findings, together with the dual role of a mixed estrogen and anti-estrogen effect, suggested that YCK and cyclophosphamide can be a potential combination in chemo-hormonal therapy for breast cancer. Copyright 2000 S. Karger AG, BaselEntities:
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Year: 2000 PMID: 10601799 DOI: 10.1159/000007257
Source DB: PubMed Journal: Chemotherapy ISSN: 0009-3157 Impact factor: 2.544