Literature DB >> 29128506

Proteoglycans remodeling in cancer: Underlying molecular mechanisms.

Achilleas D Theocharis1, Nikos K Karamanos2.   

Abstract

Extracellular matrix is a highly dynamic macromolecular network. Proteoglycans are major components of extracellular matrix playing key roles in its structural organization and cell signaling contributing to the control of numerous normal and pathological processes. As multifunctional molecules, proteoglycans participate in various cell functions during morphogenesis, wound healing, inflammation and tumorigenesis. Their interactions with matrix effectors, cell surface receptors and enzymes enable them with unique properties. In malignancy, extensive remodeling of tumor stroma is associated with marked alterations in proteoglycans' expression and structural variability. Proteoglycans exert diverse functions in tumor stroma in a cell-specific and context-specific manner and they mainly contribute to the formation of a permissive provisional matrix for tumor growth affecting tissue organization, cell-cell and cell-matrix interactions and tumor cell signaling. Proteoglycans also modulate cancer cell phenotype and properties, the development of drug resistance and tumor stroma angiogenesis. This review summarizes the proteoglycans remodeling and their novel biological roles in malignancies with particular emphasis to the underlying molecular mechanisms.
Copyright © 2017 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Cancer; Decorin; Glycosaminoglycans; Glypicans; Perlecan; Proteoglycans; Serglycin; Syndecans; Versican

Mesh:

Substances:

Year:  2017        PMID: 29128506     DOI: 10.1016/j.matbio.2017.10.008

Source DB:  PubMed          Journal:  Matrix Biol        ISSN: 0945-053X            Impact factor:   11.583


  48 in total

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8.  Decorin deficiency promotes epithelial-mesenchymal transition and colon cancer metastasis.

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9.  The synthesis and secretion of versican isoform V3 by mammalian cells: A role for N-linked glycosylation.

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Review 10.  Atomic force microscopy for revealing micro/nanoscale mechanics in tumor metastasis: from single cells to microenvironmental cues.

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