Inki P, Kujari H, Jalkanen M
Department of Medical Biochemistry, University of Turku, Finland.
Lab Invest. 1992 Mar;66(3):314-23.
Expression of syndecan, a cell surface proteoglycan, was studied in carcinomas induced by implanting chemically transformed keratinocytes and mammary epithelial cells into nude mice. By immunohistochemistry and in situ hybridization, syndecan was localized in keratinizing cells within moderate- to well-differentiated squamous cell carcinomas in a pattern resembling that of normal epidermis, whereas almost total loss of expression was detected in poorly-differentiated areas within these tumors. In anaplastic spindle cell carcinomas, syndecan expression was barely detectable. In biphasic tumors, induced by mammary epithelial cells, and consisting of cysts overlaying an adenocarcinoma, syndecan was unquely localized to differentiated epithelial structures such as secretory epithelial lining of the cysts as well as aberrant glands and ducts within the carcinoma. Based on the expression pattern of syndecan in the tumors studied, we conclude that the expression of this developmentally regulated molecule is associated with epithelial differentiation also during neoplastic growth.
通过将化学转化的角质形成细胞和乳腺上皮细胞植入裸鼠诱导产生癌,研究了细胞表面蛋白聚糖syndecan的表达。通过免疫组织化学和原位杂交,syndecan定位于中分化至高分化鳞状细胞癌的角质形成细胞中,其模式类似于正常表皮,而在这些肿瘤的低分化区域几乎检测到表达完全缺失。在间变性梭形细胞癌中,几乎检测不到syndecan表达。在由乳腺上皮细胞诱导产生的双相肿瘤中,该肿瘤由覆盖腺癌的囊肿组成,syndecan独特地定位于分化的上皮结构,如囊肿的分泌上皮内衬以及癌内异常的腺体和导管。基于所研究肿瘤中syndecan的表达模式,我们得出结论,这种受发育调节的分子的表达在肿瘤生长过程中也与上皮分化相关。