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Journal of Histochemistry and Cytochemistry, Vol. 45, 703-710, Copyright © 1997 by The Histochemical Society, Inc.

ARTICLE

Tumor Collagenase Stimulatory Factor (TCSF) Expression and Localization in Human Lung and Breast Cancers

Myriam Polettea,c, Christine Gillesb, Veronique Marchanda, Marianne Lorenzatoc, Bryan Tooled, Jean-Marie Tourniera, Stanley Zuckere, and Philippe Birembauta,c
a INSERM U 314, IFR 53, CHU Maison Blanche, Reims, France
b Vincent T. Lombardi Cancer Research Center, University Medical Center, Washington, DC
c Laboratoire Pol Bouin, CHU Maison Blanche, Reims, France
d Department of Anatomy and Cellular Biology, Tufts University Health Science School, Boston, Massachusetts
e Departments of Research and Medicine, Veterans Affairs Medical Center, Northport, Massachusetts

Correspondence to: Myriam Polette, Unité INSERM 314, 45, rue Cognacq-Jay, 51 100 Reims, France.

Tumor cell-derived collagenase stimulatory factor (TCSF) stimulates in vitro the biosynthesis of various matrix metalloproteinases involved in tumor invasion, such as interstitial collagenase, gelatinase A, and stromelysin 1. The expression of TCSF mRNAs was studied in vivo, using in situ hybridization and Northern blotting analysis, in seven normal tissues and in 22 squamous cell carcinomas of the lung, and in seven benign proliferations and in 22 ductal carcinomas of the mammary gland. By in situ hybridization, TCSF mRNAs were detected in 40 of 44 carcinomas, in pre-invasive and invasive cancer cells of both lung and breast cancers. TCSF mRNAs and gelatinase A mRNAs were both visualized in the same areas in serial sections in breast cancers, and were expressed by different cells, tumor cells, and fibroblasts. The histological results were confirmed by Northern blot analysis, which showed a higher expression of TCSF mRNAs in cancers than in benign and normal tissues. These observations support the hypothesis that TCSF is an important factor in lung and breast tumor progression. (J Histochem Cytochem 45:703-709, 1997)

Key Words: TCSF, metalloproteinases, tumor invasion


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