Cancer Research Annual Meeting 2010  Jordan
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online

[Cancer Research 53, 878-883, February 15, 1993]
© 1993 American Association for Cancer Research

This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Stearns, M. E.
Right arrow Articles by Wang, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Stearns, M. E.
Right arrow Articles by Wang, M.

Type IV Collagenase (Mr 72,000) Expression in Human Prostate: Benign and Malignant Tissue1

Mark E. Stearns2 and Min Wang

Department of Pathology, Medical College of Pennsylvania, Philadelphia, Pennsylvania 19129

The expression of type IV collagenase (Mr 72,000) has been examined in tissues from patients with benign prostatic hyperplasia (6 patients) and varying Gleason grades of malignant prostate cancer (18 patients). Immunoperoxidase labeling indicated that expression of the type IV collagenase was weak or nonexistent in benign tissue but consistently strong in the glandular and ductal epithelial cells of prostate tumors diagnosed at Gleason grades 1–8. In moderate to advanced cancer (i.e., Gleason grades 2 to 8), invasive tumor foci in the stromal tissue produced relatively modest amounts of type IV collagenase. The normal stromal tissue (i.e., fibroblasts) uniformly failed to produce detectable levels of type IV collagenase in the 24 patients examined. Northern and quantitative slot blot hybridization assays demonstrated that collagenase type IV mRNA levels were low in benign tissue and high in malignant tumors. In contrast, the stromal cells did not express significant amounts of type IV collagenase mRNA. Enzyme-linked immunosorbent assays demonstrated that the amounts of type IV collagenase protein correlated directly with the mRNA levels in the tumor tissue. The studies suggest that type IV collagenase may be selectively overexpressed by malignant, preinvasive prostatic epithelial cells.

1 Supported by NIH Grant CA58716 to M. E. S.

2 To whom requests for reprints should be addressed, at Department of Pathology, Medical College of Pennsylvania, 3300 Henry Avenue, Philadelphia, PA 19129.

Received 7/24/92. Accepted 12/ 4/92.




This article has been cited by other articles:


Home page
JNCI J Natl Cancer InstHome page
L. Xu, Y. Ding, W. J. Catalona, X. J. Yang, W. F. Anderson, B. Jovanovic, K. Wellman, J. Killmer, X. Huang, K. A. Scheidt, et al.
MEK4 Function, Genistein Treatment, and Invasion of Human Prostate Cancer Cells
J Natl Cancer Inst, August 19, 2009; 101(16): 1141 - 1155.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Pathol.Home page
Z. Dong, R. D. Bonfil, S. Chinni, X. Deng, J. C. Trindade Filho, M. Bernardo, U. Vaishampayan, M. Che, B. F. Sloane, S. Sheng, et al.
Matrix Metalloproteinase Activity and Osteoclasts in Experimental Prostate Cancer Bone Metastasis Tissue
Am. J. Pathol., April 1, 2005; 166(4): 1173 - 1186.
[Abstract] [Full Text] [PDF]


Home page
J AndrolHome page
M. J. Wilson, A. Jiang, C. Wiehr, X. Wang, A. A. Sinha, and D. Pei
Limited Processing of Pro-Matrix Metalloprotease-2 (Gelatinase A) Overexpressed by Transfection in PC-3 Human Prostate Tumor Cells: Association With Restricted Cell Surface Localization of Membrane-Type Matrix Metalloproteinase-1
J Androl, March 1, 2004; 25(2): 274 - 285.
[Abstract] [Full Text] [PDF]


Home page
J. Cell Sci.Home page
C. Fieber, P. Baumann, R. Vallon, C. Termeer, J. C. Simon, M. Hofmann, P. Angel, P. Herrlich, and J. P. Sleeman
Hyaluronan-oligosaccharide-induced transcription of metalloproteases
J. Cell Sci., January 15, 2004; 117(2): 359 - 367.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
D. Trudel, Y. Fradet, F. Meyer, F. Harel, and B. Tetu
Significance of MMP-2 Expression in Prostate Cancer: an Immunohistochemical Study
Cancer Res., December 1, 2003; 63(23): 8511 - 8515.
[Abstract] [Full Text] [PDF]


Home page
Molecular Cancer TherapeuticsHome page
U. Mahmood and R. Weissleder
Near-Infrared Optical Imaging of Proteases in Cancer
Mol. Cancer Ther., May 1, 2003; 2(5): 489 - 496.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
P. Sweeney, T. Karashima, S.-J. Kim, D. Kedar, B. Mian, S. Huang, C. Baker, Z. Fan, D. J. Hicklin, C. A. Pettaway, et al.
Anti-Vascular Endothelial Growth Factor Receptor 2 Antibody Reduces Tumorigenicity and Metastasis in Orthotopic Prostate Cancer Xenografts via Induction of Endothelial Cell Apoptosis and Reduction of Endothelial Cell Matrix Metalloproteinase Type 9 Production
Clin. Cancer Res., August 1, 2002; 8(8): 2714 - 2724.
[Abstract] [Full Text] [PDF]


Home page
Cancer Res.Home page
F. A. Attiga, P. M. Fernandez, A. T. Weeraratna, M. J. Manyak, and S. R. Patierno
Inhibitors of Prostaglandin Synthesis Inhibit Human Prostate Tumor Cell Invasiveness and Reduce the Release of Matrix Metalloproteinases
Cancer Res., August 1, 2000; 60(16): 4629 - 4637.
[Abstract] [Full Text]


Home page
JCOHome page
A. R. Nelson, B. Fingleton, M. L. Rothenberg, and L. M. Matrisian
Matrix Metalloproteinases: Biologic Activity and Clinical Implications
J. Clin. Oncol., March 1, 2000; 18(5): 1135 - 1135.
[Abstract] [Full Text] [PDF]


Home page
J. Biol. Chem.Home page
T. Sato, T. Kondo, T. Fujisawa, M. Seiki, and A. Ito
Furin-independent Pathway of Membrane Type 1-Matrix Metalloproteinase Activation in Rabbit Dermal Fibroblasts
J. Biol. Chem., December 24, 1999; 274(52): 37280 - 37284.
[Abstract] [Full Text] [PDF]


Home page
Clin. Cancer Res.Home page
J. Upadhyay, B. Shekarriz, J. A. Nemeth, Z. Dong, G. D. Cummings, R. Fridman, W. Sakr, D. J. Grignon, and M. L. Cher
Membrane Type 1-Matrix Metalloproteinase (MT1-MMP) and MMP-2 Immunolocalization in Human Prostate: Change in Cellular Localization Associated with High-Grade Prostatic Intraepithelial Neoplasia
Clin. Cancer Res., December 1, 1999; 5(12): 4105 - 4110.
[Abstract] [Full Text] [PDF]


Home page
JDRHome page
K.L. Pickett, G.J. Harber, A.A. DeCarlo, P. Louis, S. Shaneyfelt, L.J. Windsor, and M.K. Bodden
92K-GL (MMP-9) and 72K-GL (MMP-2) are Produced in vivo by Human Oral Squamous Cell Carcinomas and can Enhance FIB-CL (MMP-1) Activity in vitro
Journal of Dental Research, July 1, 1999; 78(7): 1354 - 1361.
[Abstract] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Cancer Research Clinical Cancer Research
Cancer Epidemiology Biomarkers & Prevention Molecular Cancer Therapeutics
Molecular Cancer Research Cancer Prevention Research
Cancer Prevention Journals Portal Cancer Reviews Online
Annual Meeting Education Book Meeting Abstracts Online
Copyright © 1993 by the American Association for Cancer Research.