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CXC chemokines mechanism of action in regulating tumor angiogenesis

dc.contributor.authorMoore, Bethany B.en_US
dc.contributor.authorArenberg, Douglas A.en_US
dc.contributor.authorAddison, Christina L.en_US
dc.contributor.authorKeane, Michael P.en_US
dc.contributor.authorPolverini, Peter J.en_US
dc.contributor.authorStrieter, Robert M.en_US
dc.date.accessioned2006-09-08T19:36:29Z
dc.date.available2006-09-08T19:36:29Z
dc.date.issued1998-03en_US
dc.identifier.citationMoore, Bethany B.; Arenberg, Douglas A.; Addison, Christina L.; Keane, Michael P.; Polverini, Peter J.; Strieter, Robert M.; (1998). "CXC chemokines mechanism of action in regulating tumor angiogenesis." Angiogenesis 2(2): 123-134. <http://hdl.handle.net/2027.42/41760>en_US
dc.identifier.issn0969-6970en_US
dc.identifier.issn1573-7209en_US
dc.identifier.urihttps://hdl.handle.net/2027.42/41760
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=14517468&dopt=citationen_US
dc.description.abstractThe CXC chemokines have recently been identified as a family of molecules which can regulate angiogenesis. Members of this family which contain the amino acid motif Glu–Leu–Arg in their amino terminus (ELR + ) act as angiogenic factors, while ELR − members act as angiostatic molecules. The balance of these angiogenic versus angiostatic factors is critical in regulating homeostasis. As we detail in this review, there is increasing evidence from a variety of tumor model systems to suggest that the angiogenic members of this family and their receptors may be playing an important role in the neovascular pathology of solid tumors. In contrast, the angiostatic effects of the ELR − ; family members may provide novel therapeutic strategies for treating many tumors.en_US
dc.format.extent117510 bytes
dc.format.extent3115 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherKluwer Academic Publishers; Springer Science+Business Mediaen_US
dc.subject.otherMedicine & Public Healthen_US
dc.subject.otherCardiologyen_US
dc.subject.otherOncologyen_US
dc.subject.otherOphthalmologyen_US
dc.subject.otherAngiogenesisen_US
dc.subject.otherChemokinesen_US
dc.subject.otherChemotaxisen_US
dc.subject.otherCytokinesen_US
dc.subject.otherNeovascularizationen_US
dc.subject.otherTumorigenesisen_US
dc.titleCXC chemokines mechanism of action in regulating tumor angiogenesisen_US
dc.typeArticleen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Internal Medicine (Division of Pulmonary and Critical Medicine), University of Michigan Medical School, Ann Arbor, MI, 48109-0642, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine (Division of Pulmonary and Critical Medicine), University of Michigan Medical School, Ann Arbor, MI, 48109-0642, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine (Division of Pulmonary and Critical Medicine), University of Michigan Medical School, Ann Arbor, MI, 48109-0642, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine (Division of Pulmonary and Critical Medicine), University of Michigan Medical School, Ann Arbor, MI, 48109-0642, USAen_US
dc.contributor.affiliationumSection of Oral Pathology, University of Michigan Dental School, Ann Arbor, MI, 48109-1078, USAen_US
dc.contributor.affiliationumDepartment of Internal Medicine (Division of Pulmonary and Critical Medicine), University of Michigan Medical School, Ann Arbor, MI, 48109-0642, USAen_US
dc.contributor.affiliationumcampusAnn Arboren_US
dc.identifier.pmid14517468en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/41760/1/10456_2004_Article_176940.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1023/A:1009284305061en_US
dc.identifier.sourceAngiogenesisen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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