Literature DB >> 2968986

Cell surface heparan sulfate proteoglycan and the neoplastic phenotype.

R V Iozzo1.   

Abstract

Cell surface proteoglycans are strategically positioned to regulate interactions between cells and their surrounding environment. Such interactions play key roles in several biological processes, such as cell recognition, adhesion, migration, and growth. These biological functions are in turn necessary for the maintenance of differentiated phenotype and for normal and neoplastic development. There is ample evidence that a special type of proteoglycan bearing heparan sulfate side chains is localized at the cell surface in a variety of epithelial and mesenchymal cells. This molecule exhibits selective patterns of reactivity with various constituents of the extracellular matrix and plasma membrane, and can act as growth modulator or as a receptor. Certainly, during cell division, membrane constituents undergo profound rearrangement, and proteoglycans may be intimately involved in such processes. The present work will focus on recent advances in our understanding of these complex macromolecules and will attempt to elucidate the biosynthesis, the structural diversity, the modes of cell surface association, and the turnover of heparan sulfate proteoglycans in various cell systems. It will then review the multiple proposed roles of this molecule, with particular emphasis on the binding properties and the interactions with various intracellular and extracellular elements. Finally, it will focus on the alterations associated with the neoplastic phenotype and will discuss the possible consequences that heparan sulfate may have on the growth of normal and transformed cells.

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Year:  1988        PMID: 2968986     DOI: 10.1002/jcb.240370107

Source DB:  PubMed          Journal:  J Cell Biochem        ISSN: 0730-2312            Impact factor:   4.429


  9 in total

Review 1.  The biology of perlecan: the multifaceted heparan sulphate proteoglycan of basement membranes and pericellular matrices.

Authors:  R V Iozzo; I R Cohen; S Grässel; A D Murdoch
Journal:  Biochem J       Date:  1994-09-15       Impact factor: 3.857

2.  Ultrastructural localization and internalization of proteoglycan epitopes in a human non-Hodgkin (B) lymphoma.

Authors:  J Timár; I Kovalszky; A Bánkfalvi; L Kopper
Journal:  Histochemistry       Date:  1990

3.  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 4.  Brain metastases in melanoma: roles of neurotrophins.

Authors:  Yvonne Denkins; Jane Reiland; Madhuchhanda Roy; Neeta D Sinnappah-Kang; Jennifer Galjour; Brian P Murry; Jason Blust; Rebecca Aucoin; Dario Marchetti
Journal:  Neuro Oncol       Date:  2004-04       Impact factor: 12.300

Review 5.  Proteoglycans and neoplasia.

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

6.  Cuprolinic blue visualization of cytosolic and membrane-associated glycosaminoglycans in the rat junctional epithelium and gingival epithelia.

Authors:  C Ayanoglou; S Lécolle; D Septier; M Goldberg
Journal:  Histochem J       Date:  1994-03

Review 7.  Altered proteoglycan gene expression and the tumor stroma.

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

8.  Release of basic fibroblast growth factor-heparan sulfate complexes from endothelial cells by plasminogen activator-mediated proteolytic activity.

Authors:  O Saksela; D B Rifkin
Journal:  J Cell Biol       Date:  1990-03       Impact factor: 10.539

9.  Origin and deposition of basement membrane heparan sulfate proteoglycan in the developing intestine.

Authors:  P Simon-Assmann; F Bouziges; M Vigny; M Kedinger
Journal:  J Cell Biol       Date:  1989-10       Impact factor: 10.539

  9 in total

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