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Extracellular matrix component signaling in cancer

期刊

ADVANCED DRUG DELIVERY REVIEWS
卷 97, 期 -, 页码 28-40

出版社

ELSEVIER
DOI: 10.1016/j.addr.2015.10.013

关键词

Discoidin domain receptors; Integrin; Proteoglycan; Syndecan; Adhesion; Migration

资金

  1. Danish National Research Foundation
  2. Novo Nordisk Fonden
  3. Lundbeck Fonden
  4. Danish Council of Natural Sciences
  5. Medical Research Council UK [G0701121]
  6. Biotechnology and Biological Sciences Research Council UK [BB/1011226/1]
  7. Norwegian Centre of Excellence grant [223250]
  8. BBSRC [BB/I011226/1] Funding Source: UKRI
  9. MRC [G0701121] Funding Source: UKRI
  10. Biotechnology and Biological Sciences Research Council [BB/I011226/1] Funding Source: researchfish
  11. Medical Research Council [G0701121] Funding Source: researchfish

向作者/读者索取更多资源

Cell responses to the extracellular matrix depend on specific signaling events. These are important from early development, through differentiation and tissue homeostasis, immune surveillance, and disease pathogenesis. Signaling not only regulates cell adhesion cytoskeletal organization and motility but also provides survival and proliferation cues. The major classes of cell surface receptors for matrix macromolecules are the integrins, discoidin domain receptors, and transmembrane proteoglycans such as syndecans and CD44. Cells respond not only to specific ligands, such as collagen, fibronectin, or basement membrane glycoproteins, but also in terms of matrix rigidity. This can regulate the release and subsequent biological activity of matrix-bound growth factors, for example, transforming growth factor-beta. In the environment of tumors, there may be changes in cell populations and their receptor profiles as well as matrix constitution and protein cross-linking. Here we summarize roles of the three major matrix receptor types, with emphasis on how they function in tumor progression. (C) 2015 Elsevier B.V. All rights reserved.

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