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PMID: 12475804 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. Review

CXC chemokines in angiogenesis related to pulmonary fibrosis.

Chest ·Vol. 122 ·No. 6 Suppl ·2002-12-00 ·Pages 298S-301S

Strieter RM, Belperio JA, Keane MP

Abstract

Angiogenesis, defined as the growth of new capillaries from preexisting vessels, is a pervasive biological phenomenon that is at the core of many physiologic and pathologic processes. An opposing balance of angiogenic and angiostatic factors regulates angiogenesis. Examples of physiologic processes that depend on angiogenesis include embryogenesis, wound repair, and the ovarian/menstrual cycle. In contrast, chronic inflammation associated with chronic fibroproliferative disorders as well as growth and metastasis of solid tumors are associated with aberrant angiogenesis. CXC chemokines comprise a unique cytokine family that contains members that exhibit on a structural/functional basis either angiogenic or angiostatic biological activity. In this review, we will discuss the role of CXC chemokines and angiogenesis in pulmonary fibrosis.

MeSH Terms
Chemokines, CXC/physiology Humans Lung/blood supply,physiopathology Neovascularization, Pathologic/physiopathology Pulmonary Fibrosis/physiopathology Receptors, Chemokine/physiology
Chemicals
Chemokines, CXC Receptors, Chemokine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Strieter Robert M
Department of Medicine, UCLA School of Medicine, Los Angeles, CA CA 90024-1922, USA. [email protected]
Belperio John A
Keane Michael P
Article Info
Journal
Chest
Abbr.
Chest
ISSN
0012-3692
Published
2002-12-00
Pages
298S-301S
Language
English
Region
United States
NLM ID
0231335
Subset
IM
Grants
NCI NIH HHS · CA87879 · United States
NHLBI NIH HHS · HL03906 · United States
NHLBI NIH HHS · HL04493 · United States
NHLBI NIH HHS · HL66027 · United States
NHLBI NIH HHS · P01 HL67665 · United States
NCI NIH HHS · P50 CA90388 · United States
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