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XB-ART-10606
Exp Cell Res 2000 Jul 10;2581:12-22. doi: 10.1006/excr.2000.4915.
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Differentiation of mesothelioma cells is influenced by the expression of proteoglycans.

Dobra K , Andäng M , Syrokou A , Karamanos NK , Hjerpe A .


Abstract
Malignant mesothelioma characteristically shows epithelial and/or sarcomatous morphology, this phenotypic differentiation being correlated to the prognosis. The present study was undertaken to see whether proteoglycan (PG) expression influences mesothelioma differentiation. To assess this hypothesis, we studied a mesothelioma model, where the cells were induced to differentiate into epithelial or fibroblast-like morphology, mimicking the biphasic growth of this sarcoma. Series of PGs were analyzed in parallel by semiquantitative reversed transcriptase polymerase chain reaction, showing increased expression of syndecan-2, syndecan-4, and hyaluronan synthase in the epithelial phenotype, whereas the fibroblast-like cells expressed more matrix PGs: versican, decorin, and biglycan. Western blotting confirms these differences and provides evidence of extensive shedding and rapid turnover of cell membrane PGs. Experimental down-regulation of the studied syndecans by antisense targeting resulted in a change in shape from polygonal to spindle-like morphology, while syndecan-1 and -4, but not syndecan-2, could be associated with cell aggregation, indicating distinct functions of different syndecans. The PG profile is thus closely associated with the morphology and biological behavior of tumor cells, mesotheliomas showing a different profile than true epithelial tumors.

PubMed ID: 10912783
Article link: Exp Cell Res


Species referenced: Xenopus
Genes referenced: bgn cd44 dcn gpc1 has1 hspg2 sdc1 sdc2 sdc4 vcan