Maeng Hack-Young, Choi Dong-Kug, Takeuchi Motoi, Yamamoto Masami, Tominaga Michiyo, Tsukamoto Tetsuya, Tatematsu Masae, Ito Takashi, Sakaki Yoshiyuki, Furihata Chie
Human Genome Center, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.
Jpn J Cancer Res. 2002 Sep;93(9):960-7. doi: 10.1111/j.1349-7006.2002.tb02471.x.
The present study was designed to define molecular alterations in the initiation stage of rat stomach carcinogenesis. Groups of male Lewis rats, 6 weeks old, were given drinking water with or without N-methyl-N'-nitro-N-nitrosoguanidine (MNNG; 100 mg/liter). Total RNA was isolated from the stomach pyloric mucosa, and fluorescent differential display analysis was performed. A cDNA fragment of 125 bp encoding an extracellular matrix-associated matricellular glycoprotein, osteonectin, was identified after 14 days of MNNG exposure. A severalfold increase in expression was observed after 14 and 27 days of MNNG exposure, as determined by northern blot and RT-PCR. Immunohistochemistry revealed that osteonectin-mAb-stained fibroblastic cells appeared in interstitial tissue of pyloric mucosa. Additionally the gene expression of other extracellular matrix proteins, viz., collagen type III, fibronectin, osteopontin, proteoglycan NG2, laminin gamma1 and S-laminin, was also markedly increased, as determined by competitive RT-PCR after 14 days of MNNG exposure. The gene expression of osteonectin and the six other extracellular matrix proteins was elevated in twelve stomach adenocarcinomas and adenomas induced by MNNG in Lewis and WKY rats. Osteonectin-mAb-stained fibroblastic cells were evident in interstitial tissue of stomach tumor. These results suggest that osteonectin-expressing fibroblastic cells appear in the interstitial tissue of pyloric mucosa from the early initiation stage of rat stomach chemical carcinogenesis, and that this phenomenon probably plays a role in cancer development.
本研究旨在确定大鼠胃癌发生起始阶段的分子改变。将6周龄的雄性Lewis大鼠分组,给予含或不含N-甲基-N'-硝基-N-亚硝基胍(MNNG;100 mg/升)的饮用水。从胃幽门黏膜分离总RNA,并进行荧光差异显示分析。在MNNG暴露14天后,鉴定出一个125 bp的cDNA片段,其编码一种细胞外基质相关的基质细胞糖蛋白骨连接蛋白。通过Northern印迹和RT-PCR测定,在MNNG暴露14天和27天后观察到表达增加了几倍。免疫组织化学显示,骨连接蛋白单克隆抗体染色的成纤维细胞出现在幽门黏膜的间质组织中。此外,通过竞争性RT-PCR测定,在MNNG暴露14天后,其他细胞外基质蛋白,即III型胶原、纤连蛋白、骨桥蛋白、蛋白聚糖NG2、层粘连蛋白γ1和S-层粘连蛋白的基因表达也显著增加。在Lewis和WKY大鼠中,由MNNG诱导的12个胃腺癌和腺瘤中,骨连接蛋白和其他六种细胞外基质蛋白的基因表达升高。骨连接蛋白单克隆抗体染色的成纤维细胞在胃肿瘤的间质组织中明显可见。这些结果表明,表达骨连接蛋白的成纤维细胞在大鼠胃化学致癌作用的早期起始阶段就出现在幽门黏膜的间质组织中,并且这种现象可能在癌症发展中起作用。