Literature DB >> 3997882

Neoplastic modulation of extracellular matrix. Colon carcinoma cells release polypeptides that alter proteoglycan metabolism in colon fibroblasts.

R V Iozzo.   

Abstract

Despite the growing evidence implicating proteoglycans in the control of cell proliferation and differentiation, little is known about the factors that control their metabolism in neoplasia or the mechanisms through which these macromolecules may influence neoplastic growth. The primary objective of the present study was to test whether human colon carcinoma cells released soluble mediators capable of stimulating the synthesis of proteoglycans in normal colon fibroblasts in vitro. Serum-free medium conditioned by colon carcinoma cells (TCM) was capable of stimulating several-fold the synthesis and secretion of proteoglycans in normal colon fibroblasts without inducing a mitogenic response. This effect was a true stimulation of proteoglycan biosynthesis since the kinetics of turnover were identical in the presence or absence of TCM. Characterization of the proteoglycans synthesized in the absence of TCM revealed that colon fibroblasts synthesized at least three species of proteoglycans including a heparan sulfate proteoglycan which was associated primarily with the cell layer and two populations of proteoglycans which were predominantly released into the medium and contained chondroitin-dermatan sulfate side chains. When fibroblasts were exposed to TCM, they synthesized and released higher amounts of proteoglycans which had overall similar density, molecular weight, and polydispersity but differed from controls in that they contained significantly higher proportions of chondroitin sulfate side chains. Partial characterization of TCM strongly indicated that the stimulatory activity comprised a family of polypeptides, with molecular weight between 5.4 and 6.0 X 10(5), which were heat stable and acid/alkali labile. Neoplastic modulation of proteoglycan metabolism in normal mesenchymal cells may represent an additional mechanism through which tumor cells can alter their surrounding environment.

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Year:  1985        PMID: 3997882

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  13 in total

1.  Ectopic expression of decorin protein core causes a generalized growth suppression in neoplastic cells of various histogenetic origin and requires endogenous p21, an inhibitor of cyclin-dependent kinases.

Authors:  M Santra; D M Mann; E W Mercer; T Skorski; B Calabretta; R V Iozzo
Journal:  J Clin Invest       Date:  1997-07-01       Impact factor: 14.808

2.  Fibroblastlike primary cells from human colon adenocarcinoma explants: collagen biosynthesis.

Authors:  J Turnay; N Olmo; J G Gavilanes; M A Lizarbe
Journal:  In Vitro Cell Dev Biol       Date:  1991-06

3.  De novo decorin gene expression suppresses the malignant phenotype in human colon cancer cells.

Authors:  M Santra; T Skorski; B Calabretta; E C Lattime; R V Iozzo
Journal:  Proc Natl Acad Sci U S A       Date:  1995-07-18       Impact factor: 11.205

Review 4.  Cathepsin B and other proteases in human colorectal carcinoma.

Authors:  J M Jessup
Journal:  Am J Pathol       Date:  1994-08       Impact factor: 4.307

5.  Hypomethylation of the decorin proteoglycan gene in human colon cancer.

Authors:  R Adany; R V Iozzo
Journal:  Biochem J       Date:  1991-06-01       Impact factor: 3.857

Review 6.  Shaping future strategies for the pharmacological control of tumor cell metastases.

Authors:  R G Greig; D L Trainer
Journal:  Cancer Metastasis Rev       Date:  1986       Impact factor: 9.264

Review 7.  Proteoglycans and neoplasia.

Authors:  R V Iozzo
Journal:  Cancer Metastasis Rev       Date:  1988-04       Impact factor: 9.264

8.  Mechanism of action of the migration stimulating factor produced by fetal and cancer patient fibroblasts: effect on hyaluronic and synthesis.

Authors:  S L Schor; A M Schor; A M Grey; J Chen; G Rushton; M E Grant; I Ellis
Journal:  In Vitro Cell Dev Biol       Date:  1989-08

Review 9.  Altered proteoglycan gene expression and the tumor stroma.

Authors:  R V Iozzo; I Cohen
Journal:  Experientia       Date:  1993-05-15

10.  Cytoplasmic dye transfer between metastatic tumor cells and vascular endothelium.

Authors:  M E el-Sabban; B U Pauli
Journal:  J Cell Biol       Date:  1991-12       Impact factor: 10.539

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