Please use this identifier to cite or link to this item: https://doi.org/10.1158/1535-7163.MCT-06-0082
DC FieldValue
dc.titleTherapeutic value of glycosaminoglycans in cancer
dc.contributor.authorYip, G.W.
dc.contributor.authorSmollich, M.
dc.contributor.authorGötte, M.
dc.date.accessioned2015-09-07T09:55:46Z
dc.date.available2015-09-07T09:55:46Z
dc.date.issued2006-09
dc.identifier.citationYip, G.W., Smollich, M., Götte, M. (2006-09). Therapeutic value of glycosaminoglycans in cancer. Molecular Cancer Therapeutics 5 (9) : 2139-2148. ScholarBank@NUS Repository. https://doi.org/10.1158/1535-7163.MCT-06-0082
dc.identifier.issn15357163
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/120693
dc.description.abstractGlycosaminoglycans are unbranched polysaccharides composed of repeating units of alternating uronic acids and amino sugars. Most glycosaminoglycans are covalently attached to core proteins to form proteoglycans. Posttranslational modifications result in specific motifs that bind to a large variety of ligands, thus regulating growth factor signaling, cellular behavior, inflammation, angiogenesis, and the proteolytic environment. Dysregulated expression of glycosaminoglycans is present in cancer and reported to correlate with clinical prognosis in several malignant neoplasms. Recent knowledge on the biological roles of these molecules in cancer biology, tumor angiogenesis, and metastasis has promoted the development of drugs targeting them. Pharmaceutical approaches include the use of chemically modified heparins and glycosaminoglycans with defined structures, combination of inhibitors of glycosaminoglycan biosynthesis and polyamine depletion, and biologically active glycosaminoglycan-binding peptides. In addition, glycosaminoglycans are used as tumor-specific delivery and targeting vehicles for toxins and chemotherapeutics. Encouraging results in animal studies and clinical trials show the clinical relevance of glycosaminoglycan-based drugs and the use of glycosaminoglycans as therapeutic targets. Copyright © 2006 American Association for Cancer Research.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1158/1535-7163.MCT-06-0082
dc.sourceScopus
dc.typeReview
dc.contributor.departmentANATOMY
dc.description.doi10.1158/1535-7163.MCT-06-0082
dc.description.sourcetitleMolecular Cancer Therapeutics
dc.description.volume5
dc.description.issue9
dc.description.page2139-2148
dc.description.codenMCTOC
dc.identifier.isiut000240691800001
Appears in Collections:Staff Publications

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