Plasminogen activator was recovered from bladder tumors by 30% ammonium sulfate precipitation, acid treatment and concanavalin A-Sepharose affinity chromatography to a purification factor of about 80,000. The pooled fraction from the binding protein to concanavalin A-Sepharose revealed a single enzy
The plasminogen-activation system in ovarian tumors
โ Scribed by E. Pujade-Lauraine; H. Lu; S. Mirshahi; J. Soria; C. Soria; A. Bernadou; E. K. O. Kruithof; H. R. Lijnen; P. Burtin
- Book ID
- 102868894
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- French
- Weight
- 532 KB
- Volume
- 55
- Category
- Article
- ISSN
- 0020-7136
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โฆ Synopsis
We studied the plasminogen activation system in tumor tissue by measuring the antigen level of the 2 plasminogen activators, tissue-type (t-PA) and urokinase-type (U-PA) and their inhibitors, plasminogen-activator inhibitors type-I (PAL I) and type-2 (PAI-2) in the tissue extracts of 43 human benign and malignant ovarian tumors. U-PA levels were significantly higher in malignant than in benign tumors. In addition, U-PA antigen levels were higher in the metastatic tissue of advanced disease (FIGO stage 111) than in the primary localized tumor (FIGO stage 1/11).
Also PAI-I concentrations tended to be higher in malignant than in benign tumors, but this difference was not statistically significant. In contrast, t-PA levels were lower in metastatic than in non-metastatic tumors, whereas PAL2 levels were unrelated to the stage of ovarian malignancy. These results were integrated in a plasminogen-activation-dependent malignancy index (U-PA X PAI-I /&PA). This index distinguished the different groups of benign ovarian tumors, localized and metastatic ovarian carcinomas better than U-PA levels. It could be useful as a prognostic indicator in ovarian cancer.
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