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Effects of insulin on TGF-beta 1-induced cell growth inhibition in the human hepatoma cell lines.

作者信息

Hung W C, Chuang L Y, Tsai J H, Chang C C

机构信息

Department of Biochemistry, Kaohsiung Medical College, Taiwan, R.O.C.

出版信息

Biochem Mol Biol Int. 1993 Jul;30(4):655-63.

PMID:8401323
Abstract

The effects of insulin on cell growth control by transforming growth factor beta 1 (TGF-beta 1) in human hepatoma cell lines were studied. TGF-beta 1 inhibited cell growth and DNA synthesis of Hep3B cells but not that of HA22T/VGH cells. The cell cycle-dependent p34cdc2 kinase activity was inhibited by TGF-beta 1 in a dose-dependent manner in Hep3B cells. In contrast, the p34cdc2 kinase activity of HA22T/VGH cells was not regulated by TGF-beta 1. When insulin (10(-7) M) was added simultaneously with TGF-beta 1, we found that the inhibitory effects of TGF-beta 1 on cell growth and DNA synthesis in Hep3B cells was completely blocked and the p34cdc2 kinase activity of Hep3B cells was recovered after insulin administration. Thus, cell growth inhibition by TGF-beta 1 in Hep3B hepatoma cells can be antagonized by insulin and their interaction may play an important role in the tumor progression stage of hepatocarcinogenesis.

摘要

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