Literature DB >> 9192984

Contribution of plasminogen activators and their inhibitors to the survival prognosis of patients with Dukes' stage B and C colorectal cancer.

S Ganesh1, C F Sier, M M Heerding, J H van Krieken, G Griffioen, K Welvaart, C J van de Velde, J H Verheijen, C B Lamers, H W Verspaget.   

Abstract

Despite the advances in pre-, peri- and post-operative medical care of colorectal carcinoma patients, the prognosis has improved only marginally over recent decades. Thus, additional prognostic indicators would be of great clinical value to select patients for adjuvant therapy. In previous studies we found that colorectal carcinomas have a marked increase of the urokinase-type of plasminogen activator (u-PA), and the inhibitors PAI-1 and PAI-2, whereas the tissue-type plasminogen activator (t-PA) is found to be decreased in comparison with adjacent normal mucosa. In the present study we evaluated the prognostic value of several plasminogen activation parameters, determined in both normal and carcinomatous tissue from colorectal resection specimens, for overall survival of 136 Dukes' stage B and C colorectal cancer patients, in relation to major clinicopathological parameters. Uni- and multivariate analyses indicated that a high PAI-2 antigen level in carcinoma, a low t-PA activity and antigen level and a high u-PA/t-PA antigen ratio in adjacent normal mucosa are significantly associated with a poor overall survival. A high ratio of u-PA antigen in the carcinomas and t-PA antigen in normal mucosa, i.e. u-PA(C)/t-PA(N), was found to be predictive of a poor overall survival as well. All these parameters were found to be prognostically independent of the clinicopathological parameters. Multivariate analysis of combinations of these prognostically significant plasminogen activation parameters revealed that they are important independent prognostic indicators and have in fact a better prognostic value than their separate components. Based on these combined parameters, subgroups of patients with Dukes' stage B and C colorectal cancer could be identified as having either a high or a low risk regarding overall survival. In conclusion, these findings emphasize the relevance of the intestinal plasminogen activation system for survival prognosis of patients with colorectal cancer and, in the future, might constitute a patient selection criterion for adjuvant therapy.

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Year:  1997        PMID: 9192984      PMCID: PMC2223607          DOI: 10.1038/bjc.1997.306

Source DB:  PubMed          Journal:  Br J Cancer        ISSN: 0007-0920            Impact factor:   7.640


  57 in total

1.  Regional hepatic arterial chemotherapy for colorectal cancer metastatic to the liver: the controversy continues.

Authors:  Y Z Patt
Journal:  J Clin Oncol       Date:  1993-05       Impact factor: 44.544

2.  A simple, sensitive spectrophotometric assay for extrinsic (tissue-type) plasminogen activator applicable to measurements in plasma.

Authors:  J H Verheijen; E Mullaart; G T Chang; C Kluft; G Wijngaards
Journal:  Thromb Haemost       Date:  1982-12-27       Impact factor: 5.249

3.  Evolution in the pathologic staging of carcinoma of the colon.

Authors:  R W Beart; J A van Heerden; O H Beahrs
Journal:  Surg Gynecol Obstet       Date:  1978-02

4.  Spinal cord injury: impact on clients' significant others.

Authors:  G Hart
Journal:  Rehabil Nurs       Date:  1981 Jan-Feb       Impact factor: 1.625

5.  Eosinophil infiltration of human colonic carcinomas as a prognostic indicator.

Authors:  T P Pretlow; E F Keith; A K Cryar; A A Bartolucci; A M Pitts; T G Pretlow; P M Kimball; E A Boohaker
Journal:  Cancer Res       Date:  1983-06       Impact factor: 12.701

6.  Plasminogen activators in normal tissue and carcinomas of the human oesophagus and stomach.

Authors:  C F Sier; H W Verspaget; G Griffioen; S Ganesh; H J Vloedgraven; C B Lamers
Journal:  Gut       Date:  1993-01       Impact factor: 23.059

7.  Quantitation of tissue-type plasminogen activator in human endothelial cell cultures by use of an enzyme immunoassay.

Authors:  D C Rijken; V W van Hinsbergh; E H Sens
Journal:  Thromb Res       Date:  1984-01-15       Impact factor: 3.944

8.  Prognostic value of urokinase-type plasminogen activator in 671 primary breast cancer patients.

Authors:  J A Foekens; M Schmitt; W L van Putten; H A Peters; M Bontenbal; F Jänicke; J G Klijn
Journal:  Cancer Res       Date:  1992-11-01       Impact factor: 12.701

9.  High levels of urokinase-type plasminogen activator and its inhibitor PAI-1 in cytosolic extracts of breast carcinomas are associated with poor prognosis.

Authors:  J Grøndahl-Hansen; I J Christensen; C Rosenquist; N Brünner; H T Mouridsen; K Danø; M Blichert-Toft
Journal:  Cancer Res       Date:  1993-06-01       Impact factor: 12.701

10.  Prognostic significance of histologic host response in cancer of the large bowel.

Authors:  L Nacopoulou; P Azaris; N Papacharalampous; P Davaris
Journal:  Cancer       Date:  1981-03-01       Impact factor: 6.860

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  11 in total

1.  Tissue-type plasminogen activator activity in morphologically normal tissues adjacent to gastrointestinal carcinomas is associated with the degree of tumor progression.

Authors:  Gabriel Scicolone; Viviana Sanchez; Liliana Vauthay; Federico Fuentes; Alejandro Scicolone; Lorenzo Scicolone; Melina Rapacioli; Vladimir Flores
Journal:  J Cancer Res Clin Oncol       Date:  2005-12-21       Impact factor: 4.553

2.  Proteases as prognostic markers in cancer.

Authors:  H W Verspaget
Journal:  BMJ       Date:  1998-03-14

3.  Plasminogen activator system, vascular endothelial growth factor, and colorectal cancer progression.

Authors:  E A Baker; F G Bergin; D J Leaper
Journal:  Mol Pathol       Date:  2000-12

4.  Insulinlike growth factor-I-mediated migration and invasion of human colon carcinoma cells requires activation of c-Met and urokinase plasminogen activator receptor.

Authors:  Todd W Bauer; Fan Fan; Wenbiao Liu; Marjorie Johnson; Nila U Parikh; Graham C Parry; Jennifer Callahan; Andrew P Mazar; Gary E Gallick; Lee M Ellis
Journal:  Ann Surg       Date:  2005-05       Impact factor: 12.969

5.  ARNTL2 and SERPINE1: potential biomarkers for tumor aggressiveness in colorectal cancer.

Authors:  Gianluigi Mazzoccoli; Valerio Pazienza; Anna Panza; Maria Rosa Valvano; Giorgia Benegiamo; Manlio Vinciguerra; Angelo Andriulli; Ada Piepoli
Journal:  J Cancer Res Clin Oncol       Date:  2011-12-24       Impact factor: 4.553

6.  Regulation of the human plasminogen activator inhibitor type 2 gene: cooperation of an upstream silencer and transactivator.

Authors:  Brett Stringer; Ekemini A Udofa; Toni M Antalis
Journal:  J Biol Chem       Date:  2012-02-09       Impact factor: 5.157

7.  Targeting the urokinase plasminogen activator receptor with a monoclonal antibody impairs the growth of human colorectal cancer in the liver.

Authors:  George Van Buren; Michael J Gray; Nikolaos A Dallas; Ling Xia; Sherry J Lim; Fan Fan; Andrew P Mazar; Lee M Ellis
Journal:  Cancer       Date:  2009-07-15       Impact factor: 6.860

Review 8.  Impact of proteolytic enzymes in colorectal cancer development and progression.

Authors:  László Herszényi; Loránd Barabás; István Hritz; Gábor István; Zsolt Tulassay
Journal:  World J Gastroenterol       Date:  2014-10-07       Impact factor: 5.742

9.  MMP-2 and MMP-9 in normal mucosa are independently associated with outcome of colorectal cancer patients.

Authors:  A M J Langers; H W Verspaget; L J A C Hawinkels; F J G M Kubben; W van Duijn; J J van der Reijden; J C H Hardwick; D W Hommes; C F M Sier
Journal:  Br J Cancer       Date:  2012-04-24       Impact factor: 7.640

10.  Tumor marker utility and prognostic relevance of cathepsin B, cathepsin L, urokinase-type plasminogen activator, plasminogen activator inhibitor type-1, CEA and CA 19-9 in colorectal cancer.

Authors:  László Herszényi; Fabio Farinati; Romilda Cardin; Gábor István; László D Molnár; István Hritz; Massimo De Paoli; Mario Plebani; Zsolt Tulassay
Journal:  BMC Cancer       Date:  2008-07-10       Impact factor: 4.430

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