Literature DB >> 25333340

Cell-matrix interactions: focus on proteoglycan-proteinase interplay and pharmacological targeting in cancer.

Achilleas D Theocharis1, Chrisostomi Gialeli, Panagiotis Bouris, Efstathia Giannopoulou, Spyros S Skandalis, Alexios J Aletras, Renato V Iozzo, Nikos K Karamanos.   

Abstract

Proteoglycans are major constituents of extracellular matrices, as well as cell surfaces and basement membranes. They play key roles in supporting the dynamic extracellular matrix by generating complex structural networks with other macromolecules and by regulating cellular phenotypes and signaling. It is becoming evident, however, that proteolytic enzymes are required partners for matrix remodeling and for modulating cell signaling via matrix constituents. Proteinases contribute to all stages of diseases, particularly cancer development and progression, and contextually participate in either the removal of damaged products or in the processing of matrix molecules and signaling receptors. The dynamic interplay between proteoglycans and proteolytic enzymes is a crucial biological step that contributes to the pathophysiology of cancer and inflammation. Moreover, proteoglycans are implicated in the expression and secretion of proteolytic enzymes and often modulate their activities. In this review, we describe the emerging biological roles of proteoglycans and proteinases, with a special emphasis on their complex interplay. We critically evaluate this important proteoglycan-proteinase interactome and discuss future challenges with respect to targeting this axis in the treatment of cancer.
© 2014 FEBS.

Entities:  

Keywords:  cancer progression; cathepsins; glycosaminoglycans; matrix metalloproteinases; proteoglycan-proteinase interactome; proteoglycans; serglycin; syndecans; targeting proteinases; versican

Mesh:

Substances:

Year:  2014        PMID: 25333340      PMCID: PMC5036392          DOI: 10.1111/febs.12927

Source DB:  PubMed          Journal:  FEBS J        ISSN: 1742-464X            Impact factor:   5.542


  211 in total

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2.  The increased accumulation of structurally modified versican and decorin is related with the progression of laryngeal cancer.

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Review 3.  Localizing matrix metalloproteinase activities in the pericellular environment.

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4.  Glycosaminoglycans facilitate procathepsin B activation through disruption of propeptide-mature enzyme interactions.

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7.  Sdc1 negatively modulates carcinoma cell motility and invasion.

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Journal:  Br J Cancer       Date:  2006-04-24       Impact factor: 7.640

Review 9.  Syndecans as modulators and potential pharmacological targets in cancer progression.

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Review 3.  Cysteine cathepsins: their role in tumor progression and recent trends in the development of imaging probes.

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Review 4.  Peripheral membrane associations of matrix metalloproteinases.

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Journal:  Biochim Biophys Acta Mol Cell Res       Date:  2017-04-23       Impact factor: 4.739

Review 5.  Insights into the key roles of proteoglycans in breast cancer biology and translational medicine.

Authors:  Achilleas D Theocharis; Spyros S Skandalis; Thomas Neill; Hinke A B Multhaupt; Mario Hubo; Helena Frey; Sandeep Gopal; Angélica Gomes; Nikos Afratis; Hooi Ching Lim; John R Couchman; Jorge Filmus; Ralph D Sanderson; Liliana Schaefer; Renato V Iozzo; Nikos K Karamanos
Journal:  Biochim Biophys Acta       Date:  2015-03-28

Review 6.  Matrix modeling and remodeling: A biological interplay regulating tissue homeostasis and diseases.

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7.  Neuronal activity drives FMRP- and HSPG-dependent matrix metalloproteinase function required for rapid synaptogenesis.

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Review 8.  Small Leucine-Rich Proteoglycans in Renal Inflammation: Two Sides of the Coin.

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Review 10.  A current view of perlecan in physiology and pathology: A mosaic of functions.

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