Methylcobalamin Inhibits Fibroblast Growth Factor-8 Stimulated Proliferation and Induces Apoptosis in Shionogi Carcinoma Cells

Author:

Goto 1,Katayama 2,Tanigaki 1,Fushiki 3,Nishizawa 3,Nishizawa 1

Affiliation:

1. Dept. of Pathology, Research Institute, Osaka Medical Center for Cancer and Cardiovascular Diseases, 3-3 Nakamichi 1-Chome, Higashinari, Osaka, 537-8511, Japan, E-mail address: nisizawa-ya@mc.pref.osaka.jp, Fax: 81 6 6977 6151

2. Lab. of Clinical and Experimental Pathophysiology, Graduate School of Pharmaceutical Science, Osaka University, Osaka, 565-0871, Japan

3. Research Institute for Neurological Diseases and Geriatrics, Kyoto Prefectural University of Medicine, Kyoto, 602-0841, Japan

Abstract

SC-3 cells, an androgen-dependent mouse mammary carcinoma cell line, in response to androgen stimuli, induces the secretion of fibroblast growth factor (FGF-8), which in turn increases the proliferation of these cells. We have shown previously that methylcobalamin (MeCbl) decreases the levels of FGF-8 mRNA in SC-3 cells stimulated by testosterone, inhibiting the proliferation of SC-3 cells and inducing apoptosis. In the present study, we analyzed the effects of MeCbl on SC-3 cell proliferation in response to exogenous addition of FGF-8. Thymidine incorporation showed a significant decrease in SC-3 cells cultured with MeCbl. Immunocytochemistry for single-stranded DNA (ssDNA) and DNA fragmentation analysis demonstrated that MeCbl induced apoptosis in SC-3 cells, even in the presence of FGF-8. These results show that the addition of FGF-8 stimulates the proliferation of SC-3 cells under the androgen-depleted condition and that MeCbl might be able to interfere with FGF-8 action.

Publisher

Hogrefe Publishing Group

Subject

Nutrition and Dietetics,General Medicine,Endocrinology, Diabetes and Metabolism,Medicine (miscellaneous)

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