Saito H, Morizane T, Watanabe T, Kagawa T, Miyaguchi S, Kumagai N, Tsuchiya M
Department of Internal Medicine, School of Medicine, Keio University, Tokyo, Japan.
Int J Cancer. 1991 May 10;48(2):291-6. doi: 10.1002/ijc.2910480223.
The in vitro effect of sodium butyrate (SB) on human hepatoma cell lines PLC/PRF/5, HCC-M and HCC-T was investigated. SB was added at the non-toxic but cytostatic concentration of 1 mM. In all these cell lines, SB reduced cell proliferation and changed the morphology of the cells into a fibroblast-like shape. In PLC/PRF/5, alpha-fetoprotein production and c-myc expression were inhibited. In contrast, gene expression of albumin, one of the normal liver-cell products, and that of integrated hepatitis B virus genome, was increased. In HCC-M and HCC-T, c-myc expression, which was enhanced in the naive state, was reduced. In HCC-M, fos expression was inhibited but the expression of N- and K-ras genes did not change. SB seemed to induce normal or mature properties of hepatocytes in human hepatoma cell lines.
研究了丁酸钠(SB)对人肝癌细胞系PLC/PRF/5、HCC-M和HCC-T的体外作用。以1 mM的无毒但具有细胞生长抑制作用的浓度添加SB。在所有这些细胞系中,SB均降低了细胞增殖,并使细胞形态转变为成纤维细胞样形状。在PLC/PRF/5细胞系中,甲胎蛋白的产生和c-myc的表达受到抑制。相反,正常肝细胞产物之一白蛋白以及整合型乙型肝炎病毒基因组的基因表达则增加。在HCC-M和HCC-T细胞系中,原本增强的c-myc表达降低。在HCC-M细胞系中,fos的表达受到抑制,但N-和K-ras基因的表达未发生变化。SB似乎能诱导人肝癌细胞系中的肝细胞呈现正常或成熟特性。