Cited by 192Chemokine receptors and signalingAngiogenesis and VEGF in CancerConnective Tissue Growth Factor Research

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Chemokines as Mediators of Neovascularization

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Keeley, Ellen C., Mehrad, Borna, Strieter, Robert M.·2008·Arteriosclerosis, Thrombosis, and Vascular Biology

DOI 10.1161/atvbaha.108.162925PMC PMC2735456

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Abstract

Chemokines are a superfamily of homologous heparin-binding proteins, first described for their role in recruiting leukocytes to sites of inflammation. Chemokines have since been recognized as key factors mediating both physiological and pathological neovascularization in such diverse clinical settings as malignancy, wound repair, chronic fibroproliferative disorders, myocardial ischemia, and atherosclerosis. Members of the CXC chemokine family, structurally defined as containing the ELR amino acid motif, are potent inducers of angiogenesis, whereas another subset of the CXC chemokines inhibits angiogenesis. In addition, CCL2, a CC chemokine ligand, has been implicated in arteriogenesis. In this article, we review the current literature on the role of chemokines as mediators of neovascularization.

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10.1161/res.46.4.6244120 · DOI
10.1161/circ.101.13.1519 · DOI
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Authors: Keeley, E. C., Mehrad, B., & Strieter, R. M.
Affiliations: University of Virginia (US)
ORCID: Keeley, Ellen C.
Mehrad, Borna
Strieter, Robert M.
Venue: Arteriosclerosis, Thrombosis, and Vascular Biology
Publisher: Ovid Technologies (Wolters Kluwer Health)
Published: 2008-11
Volume: 28
Issue: 11
Pages: 1928-1936
ISSN: 1079-5642 (ISSN-L)
1524-4636
DOI: 10.1161/atvbaha.108.162925
PMC: PMC2735456
OpenAlex: W2125050685
Cited by: 192
References: 142
Citations by year: 2026: 2 · 2025: 1 · 2024: 3 · 2023: 7 · 2022: 10 · 2021: 17 · 2020: 7 · 2019: 6 · 2018: 12 · 2017: 7 · 2016: 6 · 2015: 14 · 2014: 12 · 2013: 15 · 2012: 19
FWCI: 1.68
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Locations: Arteriosclerosis Thrombosis and Vascular Biology (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Heart, Lung, and Blood Institute (HL66027, HL-73848, R01HL066027, R01HL073848)
National Cancer Institute (CA-87879, R01CA087879)
Topics: Health Sciences › Medicine › Oncology › Chemokine receptors and signaling
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Connective Tissue Growth Factor Research
Keywords: chemokines, neovascularization, angiogenesis, arteriogenesis, CXC chemokines, CC chemokines, MCP-1, inflammation, wound healing, atherosclerosis, myocardial ischemia, fibroproliferative disorders, cancer
MeSH terms: Animals, Humans, Neovascularization, Pathologic, Neovascularization, Physiologic, Chemokines, Angiogenic Proteins, Endothelial Cells, Angiostatic Proteins

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Chemokines as Mediators of Neovascularization

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