| Literature DB >> 32266657 |
Barbara Bartolini1, Elena Caravà1, Ilaria Caon1, Arianna Parnigoni1, Paola Moretto1, Alberto Passi1, Davide Vigetti1, Manuela Viola2, Evgenia Karousou3.
Abstract
The biology of tumor cells strictly depends on their microenvironment architecture and composition, which controls the availability of growth factors and signaling molecules. Thus, the network of glycosaminoglycans, proteoglycans, and proteins known as extracellular matrix (ECM) that surrounds the cells plays a central role in the regulation of tumor fate. Heparan sulfate (HS) and heparan sulfate proteoglycans (HSPGs) are highly versatile ECM components that bind and regulate the activity of growth factors, cell membrane receptors, and other ECM molecules. These HS binding partners modulate cell adhesion, motility, and proliferation that are processes altered during tumor progression. Modification in the expression and activity of HS, HSPGs, and the respective metabolic enzymes results unavoidably in alteration of tumor cell microenvironment. In this light, the targeting of HS structure and metabolism is potentially a new tool in the treatment of different cancer types.Entities:
Keywords: Adhesion; Angiogenesis; Cancer; Cell growth; Extracellular matrix; Glycosaminoglycan; Growth factor; Heparan sulfate; Heparanase; Inflammation; Invasion; Metastasis; Proteoglycan; Tumor; UDP-sugars
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Year: 2020 PMID: 32266657 DOI: 10.1007/978-3-030-40146-7_7
Source DB: PubMed Journal: Adv Exp Med Biol ISSN: 0065-2598 Impact factor: 2.622