Kishima Yoshihiko, Yoshida Kenya, Enomoto Hirayuki, Yamamoto Mitsunari, Kuroda Toshifumi, Okuda Yorihide, Uyama Hirokazu, Nakamura Hideji
Department of Molecular Medicine, Osaka University Graduate School of Medicine, Yamada-oka 2-2, Suita, Osaka 565-0871, Japan.
Hepatogastroenterology. 2002 Nov-Dec;49(48):1639-44.
BACKGROUND/AIMS: Human hepatoma-derived growth factor, purified from the conditioned medium of hepatoma-derived cell line, HuH-7, stimulates the growth of Swiss 3T3 fibroblasts and HuH-7 cells. To evaluate the role of hepatoma-derived growth factor on the growth of hepatoma cells, we investigated the effects of recombinant hepatoma-derived growth factor protein and hepatoma-derived growth factor antisense oligonucleotides on the proliferation of several hepatoma cell lines.
We examined the effects of hepatoma-derived growth factor antisense oligonucleotides on the growth of hepatoma cells by cell growth assay.
Hepatoma-derived growth factor stimulated the proliferation of some hepatoma cells (HuH-7, HLF, HepG2, AH66tc cells) about 15-70% over than the control. Hepatoma-derived growth factor antisense oligonucleotides, phosphorothioate-linked or encapsulated in liposome, can inhibit the growth of hepatoma cells. The ID50 of hepatoma-derived growth factor antisense phosphorothioate oligonucleotides for HuH-7 cells, in which hepatoma-derived growth factor expression was abundant, was 3 microM by the assay of cell proliferation and [3H]-thymidine incorporation. Their ID50 for AH66tc cells, on which the effects of exogenous hepatoma-derived growth factor were weak, was higher than 10 microM. To omit the toxic effects due to phosphorothioate modification of oligonucleotides and keep the cellular uptake more without their destruction in the culture medium, we used oligonucleotides encapsulated in cationic liposome. Hepatoma-derived growth factor antisense oligonucleotides encapsulated in liposome suppressed the growth of hepatoma cells effectively (ID50:2.0 microM).
These findings suggest that hepatoma-derived growth factor is one of important autocrine, and/or intracrine factors for hepatoma cells, and that hepatoma-derived growth factor anti-sense oligonucleotides may be useful for human hepatocellular carcinoma as an anti-cancer agent.
背景/目的:从肝癌衍生细胞系HuH-7的条件培养基中纯化得到的人肝癌衍生生长因子,可刺激瑞士3T3成纤维细胞和HuH-7细胞的生长。为评估肝癌衍生生长因子在肝癌细胞生长中的作用,我们研究了重组肝癌衍生生长因子蛋白和肝癌衍生生长因子反义寡核苷酸对几种肝癌细胞系增殖的影响。
我们通过细胞生长试验检测了肝癌衍生生长因子反义寡核苷酸对肝癌细胞生长的影响。
肝癌衍生生长因子刺激某些肝癌细胞(HuH-7、HLF、HepG2、AH66tc细胞)的增殖比对照高出约15%-70%。硫代磷酸酯连接或包裹在脂质体中的肝癌衍生生长因子反义寡核苷酸可抑制肝癌细胞的生长。通过细胞增殖和[3H] - 胸腺嘧啶核苷掺入试验,肝癌衍生生长因子硫代磷酸酯反义寡核苷酸对HuH-7细胞(其中肝癌衍生生长因子表达丰富)的ID50为3 microM。它们对AH66tc细胞(外源性肝癌衍生生长因子对其作用较弱)的ID50高于10 microM。为避免寡核苷酸硫代磷酸酯修饰带来的毒性作用,并在不破坏培养基的情况下使细胞摄取更多,我们使用包裹在阳离子脂质体中的寡核苷酸。包裹在脂质体中的肝癌衍生生长因子反义寡核苷酸有效抑制了肝癌细胞的生长(ID50:2.0 microM)。
这些发现表明,肝癌衍生生长因子是肝癌细胞重要的自分泌和/或内分泌因子之一,并且肝癌衍生生长因子反义寡核苷酸作为抗癌剂可能对人类肝细胞癌有用。