Ito H, Hata J, Yokozaki H, Tahara E
Section of Clinical Pathology, Kure Mutual Aid Hospital.
Gan No Rinsho. 1987 Aug;33(10):1266-73.
The heterogeneity of gastrin-containing G cells present in human gastric mucosa has been examined immunohistochemically. Calcitonin gene-related peptide (CGRP), calcitonin and human chorionic gonadotropin (hCG)-immunoreactivity were detected in about 500, 20 and 10 cells pro 1,000 G cells, respectively, these findings supporting the "one cell, multi-hormone theory". Gastrin, calcitonin immunoreactive tumor cells were demonstrated in 13%, 3% of the antral adenocarcinomas and 17% and 10% of antral endocrine tumors, but they were not found in fundic adenocarcinomas and endocrine tumors. Cell hybridization between the tumor cell and the G-cell might be a possible mechanism for the occurrence of gastric and calcitonin in the gastric tumors. HCG-immunoreactive tumor cells were detected in 27% of antral adenocarcinomas, and in 24% of the fundic adenocarcinomas, and the production of hCG by gastric tumor cells might be based on the gene expression during carcinogenesis, regardless of the tumor localization.
已采用免疫组织化学方法研究了人胃黏膜中含胃泌素的G细胞的异质性。降钙素基因相关肽(CGRP)、降钙素和人绒毛膜促性腺激素(hCG)免疫反应性分别在每1000个G细胞中约500、20和10个细胞中检测到,这些发现支持“一个细胞,多种激素理论”。胃泌素、降钙素免疫反应性肿瘤细胞在13%的胃窦腺癌、3%的胃窦内分泌肿瘤、17%和10%的胃窦内分泌肿瘤中被证实,但在胃底腺癌和内分泌肿瘤中未发现。肿瘤细胞与G细胞之间的细胞杂交可能是胃肿瘤中出现胃泌素和降钙素的一种可能机制。HCG免疫反应性肿瘤细胞在27%的胃窦腺癌和24%的胃底腺癌中被检测到,胃肿瘤细胞产生hCG可能基于致癌过程中的基因表达,而与肿瘤定位无关。