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Lewis肺癌中的1型纤溶酶原激活物抑制剂

Plasminogen activator inhibitor-type 1 in Lewis lung carcinoma.

作者信息

Kristensen P, Pyke C, Lund L R, Andreasen P A, Danø K

机构信息

Finsen Laboratory, Rigshospitalet, Copenhagen, Denmark.

出版信息

Histochemistry. 1990;93(6):559-66. doi: 10.1007/BF00272198.

Abstract

Plasminogen activator inhibitor-type 1 (PAI-1) was identified in extracts of Lewis lung carcinoma, and its immunohistochemical localization was studied together with that of urokinase-type (u-PA) and tissue-type (t-PA) plasminogen activators. All primary tumors (n = 11) contained heterogeneously distributed immunoreactivity against each of the three components. Most often, areas that contained u-PA immunoreactivity also contained PAI-1 immunoreactivity. However, several areas showed a strong u-PA immunoreactivity, but no or low PAI-1 immunoreactivity. The latter staining pattern was only found in peripheral areas, and usually in areas with histological signs of tissue destruction. Lung metastases always contained u-PA immunoreactivity, while PAI-1 immunoreactivity was found in most, but not all, metastases. t-PA immunoreactivity was found in a few scattered tumor cells, in primary carcinomas as well as metastases. Controls that included absorption with highly purified antigen preparations and immunoblotting, indicated that all the immunoreactivity represented genuine PAI-1, u-PA and t-PA, respectively. The results are consistent with an assumption that the plasminogen activation system, and particularly u-PA and PAI-1, plays a role in regulation of breakdown of extracellular matrix proteins during invasive growth in this carcinoma.

摘要

纤溶酶原激活物抑制剂 -1(PAI -1)是在Lewis肺癌提取物中鉴定出来的,其免疫组织化学定位与尿激酶型(u -PA)和组织型(t -PA)纤溶酶原激活物一起进行了研究。所有原发性肿瘤(n = 11)对这三种成分中的每一种都含有异质性分布的免疫反应性。最常见的是,含有u -PA免疫反应性的区域也含有PAI -1免疫反应性。然而,有几个区域显示出强烈的u -PA免疫反应性,但没有或只有低水平的PAI -1免疫反应性。后一种染色模式仅在外周区域发现,通常在有组织破坏组织学迹象的区域。肺转移瘤总是含有u -PA免疫反应性,而在大多数但并非所有转移瘤中都发现了PAI -1免疫反应性。在原发性癌和转移瘤中的一些散在肿瘤细胞中发现了t -PA免疫反应性。包括用高度纯化的抗原制剂进行吸收和免疫印迹的对照表明,所有免疫反应性分别代表真正的PAI -1、u -PA和t -PA。这些结果与纤溶酶原激活系统,特别是u -PA和PAI -1在该癌侵袭性生长过程中细胞外基质蛋白降解调节中起作用的假设一致。

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