Leung J P, Nelson-Rees W A, Moore G E, Cailleau R, Edgington T S
Int J Cancer. 1981 Jul 15;28(1):35-42. doi: 10.1002/ijc.2910280107.
The presence, concentration and selected molecular characteristics of the human mammary carcinoma glycoprotein molecule set MTGP, a trace and apparently tumor-specific molecule, were examined in fifteen cell cultures established from mammary carcinomas, tissue from seven mammary carcinomas and control cultures. Both cytosol and membrane-associated forms of MTGP were analyzed, and each was phenotyped by reference to isoelectric point and buoyant density. All cells or tissues of mammary carcinoma origin contained membrane MTGP, whereas cytosol MTGP was undetectable in cell cultures from half of the mammary carcinomas. Neither membrane nor cytosol MTGP were detectable in cells other than mammary carcinomas. Cytosol MTGP could be assigned to three groups by reference to presence, isoelectric point and buoyant density. Membrane MTGP also exhibited heterogeneity between different tumors and could be assigned to three groups by isoelectric point and buoyant density. Each form of MTGP was homogeneous for a given single tumor or cell culture and retained its phenotypic features with passage and cloning. Four general types of MTGP are proposed, through there may be additional fine heterogeneity that cannot be further resolved at this time. These data provide an initial characterization of the membrane form of MTGP and an integrated characterization that is consistent with the concept that tumor-specific antigens may possess both constant regions by reference to antigens recognized by the antisera and variable structure by reference to physicochemical characteristics.
对一组微量且明显具有肿瘤特异性的人乳腺癌糖蛋白分子(MTGP)的存在、浓度及选定的分子特征进行了检测,检测对象包括15种源自乳腺癌的细胞培养物、7例乳腺癌组织以及对照培养物。对MTGP的胞质溶胶形式和膜相关形式均进行了分析,并根据等电点和浮力密度对每种形式进行了表型鉴定。所有源自乳腺癌的细胞或组织均含有膜MTGP,而在半数乳腺癌的细胞培养物中未检测到胞质溶胶MTGP。除乳腺癌细胞外,在其他细胞中均未检测到膜MTGP和胞质溶胶MTGP。根据其存在情况、等电点和浮力密度,可将胞质溶胶MTGP分为三组。不同肿瘤之间的膜MTGP也表现出异质性,根据等电点和浮力密度可将其分为三组。对于给定的单个肿瘤或细胞培养物,每种形式的MTGP都是均一的,并且在传代和克隆过程中保留其表型特征。虽然可能存在目前无法进一步分辨的其他细微异质性,但仍提出了四种一般类型的MTGP。这些数据提供了MTGP膜形式的初步特征描述以及一个综合特征描述,这与肿瘤特异性抗原可能具有恒定区域(参照抗血清识别的抗原)和可变结构(参照物理化学特征)这一概念相一致。