Albrechtsen R, Nielsen M, Wewer U, Engvall E, Ruoslahti E
Cancer Res. 1981 Dec;41(12 Pt 1):5076-81.
The distribution of the basement membrane glycoprotein laminin was studied by the immunoperoxidase technique in benign and malignant human breast tissue and in axillary lymph nodes from patients with breast cancer. An antiserum prepared against rat laminin was used. The specificity of this antiserum against human laminin was studied using the FL cell line of human epithelial-like cells derived from normal amniotic membrane. The antiserum reacted with these cells in immunoperoxidase staining and precipitated metabolically labeled secreted polypeptides which comigrated with polypeptides with molecular weights of 400,000 and 200,000 of rat laminin in sodium dodecyl sulfate:polyacrylamide gel electrophoresis. The neoplastic cells in malignant breast tissues showed strong cytoplasmic staining for laminin, and a positive reaction was aslo found in lymph node metastases. In some cases in which only micrometastases were present, these cells also stained strongly for laminin. In nonmalignant breast tissues, the epithelial cells of the duct were positive for laminin, but the staining was weaker than in the carcinomas. Pretreatment of the fixed tissue sections with trypsin markedly enhanced the staining of basement membranes for laminin. In trypsin-treated sections of normal breast tissue and benign lesions, the laminin staining delineated continuous basement membranes. In carcinomas representing the more differentiated types, basement membranes presumably produced by the tumor cells could be revealed by laminin staining, but they were thinner and discontinuous. The poorly differentiated carcinomas lacked organized basement membranes detectable by laminin staining. Our studies suggest that staining for laminin may be a useful adjunct test for detection of micrometatases in lymph nodes. The correlation of disintegration of the laminin-containing basement membranes of tumors with increasingly anaplastic appearance supports the notion that basement membranes may play a role in tumor invasion.
采用免疫过氧化物酶技术,研究了基底膜糖蛋白层粘连蛋白在人乳腺良恶性组织及乳腺癌患者腋窝淋巴结中的分布情况。使用了针对大鼠层粘连蛋白制备的抗血清。利用源自正常羊膜的人上皮样细胞系FL细胞,研究了该抗血清对人层粘连蛋白的特异性。在免疫过氧化物酶染色中,该抗血清与这些细胞发生反应,并沉淀出代谢标记的分泌性多肽,这些多肽在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳中与大鼠层粘连蛋白分子量为400,000和200,000的多肽迁移率相同。恶性乳腺组织中的肿瘤细胞层粘连蛋白呈强细胞质染色,在淋巴结转移灶中也发现了阳性反应。在某些仅存在微转移的病例中,这些细胞层粘连蛋白染色也很强。在非恶性乳腺组织中,导管上皮细胞层粘连蛋白呈阳性,但染色比癌组织弱。用胰蛋白酶预处理固定组织切片可显著增强基底膜层粘连蛋白的染色。在正常乳腺组织和良性病变的胰蛋白酶处理切片中,层粘连蛋白染色勾勒出连续的基底膜。在分化程度较高的癌组织中,层粘连蛋白染色可显示肿瘤细胞可能产生的基底膜,但它们较薄且不连续。低分化癌缺乏层粘连蛋白染色可检测到的有组织的基底膜。我们的研究表明,层粘连蛋白染色可能是检测淋巴结微转移的一种有用辅助检测方法。含层粘连蛋白的肿瘤基底膜解体与肿瘤间变外观增加的相关性支持了基底膜可能在肿瘤侵袭中起作用的观点。