Livingstone J I, Filipe M I, Wastell C
Academic Surgical Unit, Chelsea and Westminster Hospital, London.
Gut. 1994 May;35(5):604-7. doi: 10.1136/gut.35.5.604.
The induction of adenocarcinomas in the glandular stomach of the adult male Wistar rat by N-methyl-N'-nitro-N-nitrosoguanidine (MNNG) was used as a model to study the expression of the growth promoting peptide, transforming growth factor alpha (TGF alpha), during experimental gastric carcinogenesis. TGF alpha was identified using the monoclonal antibody Ab-2 and standard immunohistochemistry, together with a semiquantitative assessment of the intensity of expression. Immunoreactivity was confined to the differentiated compartment of the mucosa while the carcinogen MNNG caused a significant increase in the intensity of TGF alpha expression (p < 0.01), after as little as 16 weeks' exposure. In experimental adenocarcinomas, a change to a previously undescribed pattern of perinuclear TGF alpha expression was found, which may represent the site of intense TGF alpha production in the Golgi apparatus after malignant transformation.
采用N-甲基-N'-硝基-N-亚硝基胍(MNNG)诱导成年雄性Wistar大鼠腺胃腺癌,作为研究实验性胃癌发生过程中促生长肽转化生长因子α(TGFα)表达的模型。使用单克隆抗体Ab-2和标准免疫组织化学方法鉴定TGFα,并对表达强度进行半定量评估。免疫反应性局限于黏膜的分化区,而致癌物MNNG在暴露仅16周后就导致TGFα表达强度显著增加(p < 0.01)。在实验性腺癌中,发现了一种以前未描述的核周TGFα表达模式的变化,这可能代表了恶性转化后高尔基体中TGFα大量产生的部位。