In experimental models, plasminogen activator-mediated degradation of the extracellular matrix is inhibited by type-1 plasminogen activator inhibitor (PAI-1). PA14 has also been shown to protect tumour stromal tissue from autoproteolytic activities and may thus substantially promote tumour growth an
Plasminogen activator inhibitor 1 in human carcinoma tissues
โ Scribed by Nobuya Tanaka; Hideharu Fukao; Shigeru Ueshima; Kiyotaka Okada; Masayuki Yasutomi; Osamu Matsuo
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- French
- Weight
- 577 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
Abstract
The content of PAIโ1 was measured in carcinoma tissues from the stomach and colorectum divided macroscopically into 3 portions: the central part of the carcinoma, the marginal part of the carcinoma containing some normal mucosa, and the normal mucosa. Among these tissues, the highest levels of PAIโ1 antigen were found in the central part of the carcinoma. On the other hand, no PAIโ1 antigen or activity was observed in the normal mucosae. The PAIโ1 produced in the stomach and colorectal carcinoma tissues showed a nonโlytic zone with a molecular weight of 54 kDa by reverse fibrin autography, and this 54โkDa band reacted with antiโPAIโ1 IgG on an immunoblotted nitrocellulose membrane by the avidinbiotin complex method. The contents of PAIโ2 in the carcinoma tissues were not significantly different from those in the normal mucosa of the stomach and colorectum. In both the stomach and colorectal carcinomas, the highest value of uโPA/total PA (sum of uโPA and tโPA) was observed in the central part of the carcinoma, followed by the marginal part of the carcinoma, and was lowest in the normal mucosa. We conclude that increased levels of PAIโ1 in malignant tissue of the stomach and colorectal tract may serve to modulate extraโcellular proteolysis by uโPA.
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