Abstract

Earlier isolated plant polyphenol PI, which is carcinostatic on mice implanted with Ehrlich carcinoma [S. Takeuchi et al., Agric. Biol. Chem., 50, 569 (1986)], showed transient, nonspecific, non-cytotoxic growth inhibition in vitro on both normal and malignant cells. Examination of its effects on alteration of native and TPA-induced in vitro phenotypes revealed that PI suppress both the plasmin and ODC activities of the cells that increase with spontaneous malignancy, and also the TPA-induced ODC activity increase. TPA-induced decrease of 125I-mEGF-binding ability was reversed by PI, to larger extent in the HeLa cells than in the untransformed RME-5–3–1 cells.

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