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      Endogenous Matrix-Derived Inhibitors of Angiogenesis

      review-article
      1 , * , 2 , 3
      Pharmaceuticals
      MDPI
      angiogenesis, extracellular matrix, collagen, cancer, therapy, biomarker

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          Abstract

          Endogenous inhibitors of angiogenesis are proteins or fragments of proteins that are formed in the body, which can inhibit the angiogenic process. These molecules can be found both in the circulation and sequestered in the extracellular matrix (ECM) surrounding cells. Many matrix-derived inhibitors of angiogenesis, such as endostatin, tumstatin, canstatin and arresten, are bioactive fragments of larger ECM molecules. These substances become released upon proteolysis of the ECM and the vascular basement membrane (VBM) by enzymes of the tumor microenvironment. Although the role of matrix-derived angiogenesis inhibitors is well studied in animal models of cancer, their role in human cancers is less established. In this review we discuss the current knowledge about these molecules and their potential use as cancer therapeutics and biomarkers.

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          Most cited references103

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          Angiogenesis in cancer, vascular, rheumatoid and other disease.

          J Folkman (1995)
          Recent discoveries of endogenous negative regulators of angiogenesis, thrombospondin, angiostatin and glioma-derived angiogenesis inhibitory factor, all associated with neovascularized tumours, suggest a new paradigm of tumorigenesis. It is now helpful to think of the switch to the angiogenic phenotype as a net balance of positive and negative regulators of blood vessel growth. The extent to which the negative regulators are decreased during this switch may dictate whether a primary tumour grows rapidly or slowly and whether metastases grow at all.
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            Basement membranes: structure, assembly and role in tumour angiogenesis.

            In recent years, the basement membrane (BM)--a specialized form of extracellular matrix (ECM)--has been recognized as an important regulator of cell behaviour, rather than just a structural feature of tissues. The BM mediates tissue compartmentalization and sends signals to epithelial cells about the external microenvironment. The BM is also an important structural and functional component of blood vessels, constituting an extracellular microenvironment sensor for endothelial cells and pericytes. Vascular BM components have recently been found to be involved in the regulation of tumour angiogenesis, making them attractive candidate targets for potential cancer therapies.
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              MMP-9 supplied by bone marrow-derived cells contributes to skin carcinogenesis.

              The matrix metalloproteinase MMP-9/gelatinase B is upregulated in angiogenic dysplasias and invasive cancers of the epidermis in a mouse model of multi-stage tumorigenesis elicited by HPV16 oncogenes. Transgenic mice lacking MMP-9 show reduced keratinocyte hyperproliferation at all neoplastic stages and a decreased incidence of invasive tumors. Yet those carcinomas that do arise in the absence of MMP-9 exhibit a greater loss of keratinocyte differentiation, indicative of a more aggressive and higher grade tumor. Notably, MMP-9 is predominantly expressed in neutrophils, macrophages, and mast cells, rather than in oncogene-positive neoplastic cells. Chimeric mice expressing MMP-9 only in cells of hematopoietic origin, produced by bone marrow transplantation, reconstitute the MMP-9-dependent contributions to squamous carcinogenesis. Thus, inflammatory cells can be coconspirators in carcinogenesis.
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                Author and article information

                Journal
                Pharmaceuticals (Basel)
                Pharmaceuticals (Basel)
                pharmaceuticals
                Pharmaceuticals
                MDPI
                1424-8247
                28 September 2010
                October 2010
                : 3
                : 10
                : 3021-3039
                Affiliations
                [1 ]Department of Surgery, Umea University Hospital, Umea University, SE-90185 Umea, Sweden;
                [2 ]Department of Diagnostics and Oral Medicine, Institute of Dentistry, University of Oulu, Oulu, Finland; E-Mail: pia.nyberg@ 123456oulu.fi (P.N.)
                [3 ]Department of Oncology, Institute of Medicine, Haukeland University Hospital, University of Bergen, Bergen, Norway; E-Mail: hans.eikesdal@ 123456biomed.uib.no (H.P.E.)
                Author notes
                [* ]Author to whom correspondence should be addressed; E-Mail: malin.sund@ 123456surgery.umu.se ; Tel.: +46-90-7850000; Fax: +46-90-7851156.
                Article
                pharmaceuticals-03-03021
                10.3390/ph3103021
                4034081
                2e93d2a8-6f3c-446d-bd7c-ef9641abf10e
                © 2010 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license ( http://creativecommons.org/licenses/by/3.0/).

                History
                : 10 August 2010
                : 19 September 2010
                : 25 September 2010
                Categories
                Review

                angiogenesis,extracellular matrix,collagen,cancer,therapy,biomarker

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