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1997 Fiscal Year Final Research Report Summary

Prevention of hepatic carcinogenesis and treatment of hepatoma by way of inhibition of the activation of Ras oncogene

Research Project

Project/Area Number 07670599
Research Category

Grant-in-Aid for Scientific Research (C)

Allocation TypeSingle-year Grants
Section一般
Research Field Gastroenterology
Research InstitutionKyushu University

Principal Investigator

SAKAI Hironori  Kyushu University・Faculty of Medicine, Assist.Prof., 医学部, 講師 (70196046)

Co-Investigator(Kenkyū-buntansha) ISOBE Hidehiko  Kyushu University・Faculty of Medicine, Assist.Prof., 医学部, 助手 (60253407)
Project Period (FY) 1995 – 1997
KeywordsRas Protein / HMG-CoA Reductase Inibiter / Hepatoma
Research Abstract

HMG-CoA reductase inhibiters inhibit the mevalonic pathway and then regulate the function of Ras protein. We tried to exhibit that they were able to inhibit the growth of hepatocyte and some kinds of hepatoma cell lines and that they had the possible therapeutic effect on hepatocellular carcinoma.
1. Simvastasin inhibited the growth of hepatoma cell lines (Hep G2, HuH-7, HLE, PLC/PRF/5) as a dose dependent manner. The extents of inhibition of growth were all most same among these cell lines.
2. Pravastatin did not have inhibitory effects of growth of all these cell lines. Since hepatoma cell lines did not have anion transporter system to transfer pravastatin into cells, pravastatin failed to inhibit the growth of these cells.
3. The inhibitory effect of simvastatin on hepatoma cell growth was nearly prevented in the presence of sufficient amount of exogenous mevalonic acid. So it was obvious that the mevalonic pathway was required for the growth of these cell lines. But neither farnesol nor isopentenyl adenine prevented the simvastatin induced inhibition of the growth of these cell lines.
4. Clinical trial of HMG-CoA reductase inhibiter administrated to patients with hepatocellular carcinoma revealed that simvastatin possibly had a therapeutic effects but pravastatin did not have.

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Published: 1999-12-08  

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