Shishido T, Yasoshima T, Hirata K, Denno R, Mukaiya M, Ura H, Yamaguchi K, Kawaguchi S, Sato N
First Department of Surgery, Sapporo Medical University School of Medicine, Japan.
Surg Today. 1999;29(6):519-25. doi: 10.1007/BF02482346.
To investigate of human pancreatic cancer metastasis to the liver, a pancreatic carcinoma line, HPC-3, was injected into the spleens of nude mice. The cells from a few liver metastatic foci of the mice injected with HPC-3 were expanded in vitro and subsequently injected into the spleens of nude mice. By repeating these procedures, we were able to obtain a cell line, designated HPC-3H4. The mice were observed to have liver metastasis in 6 of 6 (100%) cases injected with HPC-3H4, whereas the rate was 0% at 3 weeks after the intrasplenic injection of HPC-3. The tumorigenicity of HPC-3H4 was more rapid than that of HPC-3. The motile activity of HPC-3H4 was also stronger than that of HPC-3, and the adhesion to the extracellular matrix of HPC-3H4 was stronger than that of HPC-3. We also analyzed the cell surface expression of the metastasis-related adhesion molecules. As a result, no substantial changes were observed in the expression level of adhesion molecules. These results suggest that HPC-3H4 is useful for studies aimed at the prevention of liver metastasis.
为了研究人类胰腺癌向肝脏的转移,将一种胰腺癌细胞系HPC - 3注射到裸鼠的脾脏中。从注射了HPC - 3的小鼠的一些肝脏转移灶中获取细胞,在体外进行扩增,随后再注射到裸鼠的脾脏中。通过重复这些步骤,我们获得了一个细胞系,命名为HPC - 3H4。观察发现,注射HPC - 3H4的6只小鼠(100%)均出现肝脏转移,而注射HPC - 3后3周时肝脏转移率为0%。HPC - 3H4的致瘤性比HPC - 3更快。HPC - 3H4的运动活性也比HPC - 3更强,并且HPC - 3H4对细胞外基质的黏附力比HPC - 3更强。我们还分析了转移相关黏附分子的细胞表面表达。结果发现,黏附分子的表达水平没有明显变化。这些结果表明,HPC - 3H4对于旨在预防肝脏转移的研究是有用的。