Adhesion proteins, cellular morphology and fibrous components around the cell/extracellular-matrix interface in myxoid liposarcomas

Citation
T. Fukuda et M. Tsuneyoshi, Adhesion proteins, cellular morphology and fibrous components around the cell/extracellular-matrix interface in myxoid liposarcomas, J CANC RES, 126(6), 2000, pp. 320-324
Citations number
7
Categorie Soggetti
Onconogenesis & Cancer Research
Journal title
JOURNAL OF CANCER RESEARCH AND CLINICAL ONCOLOGY
ISSN journal
01715216 → ACNP
Volume
126
Issue
6
Year of publication
2000
Pages
320 - 324
Database
ISI
SICI code
0171-5216(200006)126:6<320:APCMAF>2.0.ZU;2-F
Abstract
We examined the cell/extracellular-matrix interface in 13 myxoid liposarcom as by determining the distribution of collagen and reticular fibers in the myxoid matrix, the presence of adhesion proteins and the morphological feat ures of the cytoplasmic border. Adhesion proteins (fibronectin, integrin al pha 3) and the cytoplasmic border were examined by immunofluorescence and a differential interference-contrast image analysis respectively. A network of reticular fibers and collagen fibers was present in the myxoid matrix of 11 cases (85%) and 3 cases (23%) respectively. Tumor cells with dendritic cytoplasmic processes were observed in 8 cases (62%). Adhesion proteins wer e sparsely present in tumor cells and there was no correlation between thos e proteins and collagen fibers, reticular fibers or cytoplasmic processes. Collagen fibers, dense reticular fibers or well-developed cytoplasmic proce sses were more frequently observed in the cases of long-term-surviving pati ents than those with recently developed tumors or patients who died. All 3 cases positive for collagen fibers also contained both dense reticular fibe rs and cytoplasmic processes. Our findings suggest that the fibrous compone nts in the myxoid matrix and the well-developed cytoplasmic processes may l imit the invasiveness of malignant cells. This peculiar architecture may al so explain the slowly progressive nature of myxoid liposarcomas.