Fibrillary co-deposition of laminin-5 and large unspliced tenascin-C in the invasive front of oral squamous cell carcinoma in vivo and in vitro

Citation
A. Berndt et al., Fibrillary co-deposition of laminin-5 and large unspliced tenascin-C in the invasive front of oral squamous cell carcinoma in vivo and in vitro, J CANC RES, 127(5), 2001, pp. 286-292
Citations number
42
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
ISSN journal
01715216 → ACNP
Volume
127
Issue
5
Year of publication
2001
Pages
286 - 292
Database
ISI
SICI code
0171-5216(200105)127:5<286:FCOLAL>2.0.ZU;2-#
Abstract
Purpose: Invasion of oral squamous cell carcinoma (OSCC) is associated with laminin-5 (Ln-5) synthesis, focal Ln-5 loss from the basement membrane (BM ), and Ln-5 depositions in the stroma beneath invading carcinoma cell compl exes. Methods: The study is focused on the laminin-5 matrix reorganisation within the stroma of the OSCC invasive front outside the basement membrane region as well as in OSCC-fibroblast co-culture in relation to unspliced te nascin-C (Tn-C-L) and ED-B+ fibronectin (ED-B+ fn) using confocal laser sca nning microscopy. Resulrs: In vivo Ln-5 was demonstrated as fibrillary depo sition in the invasive front. It was co-localised to Tn-C-L. In pure OSCC c ultures, Ln-5 was synthesised and deposited as a spot-like matrix. Fibrilla ry structures were not found. In contrast, in the OSCC-fibroblast co-cultur e, a fibrillary Ln-5 matrix organisation was revealed within the interface of OSCC cell-fibroblast complexes exclusively in co-distribution with Tn-C- L and ED-B+ fn. Conclusion: At least in vitro, a carcinoma cell-stroma fibr oblast intel action is indispensable for fibrillary Ln-5/Tn-C-L matrix orga nisation. Behind the parallels to the initial basement membrane formation i n organotypic cultures, the fibrillary multiprotein complexes at the OSCC c ell-fibroblast interface are suggested as provisional basement membrane fra gments with a possible supportive role for invasive tumour behaviour.