Open Access
Open access
volume 13 issue 2 pages 33

Advances in CXCR7 Modulators

Publication typeJournal Article
Publication date2020-02-21
scimago Q1
wos Q1
SJR1.019
CiteScore7.7
Impact factor4.8
ISSN14248247
PubMed ID:  32098047
Drug Discovery
Pharmaceutical Science
Molecular Medicine
Abstract

CXC chemokine receptor 7 (CXCR7) is a G-protein-coupled receptor that signals through the β-arrestin pathway. Its ligands include interferon-inducible T cell α chemoattractant (CXCL11) and stromal cell-derived factor-1 (CXCL12). It interacts with CXCR4, and the two are associated with various cancers, as well as other disease states such as coronary artery disease, stroke, inflammation and human immunodeficiency virus (HIV). Antibodies and small interfering RNA (siRNA) have shown the utility of antagonists of CXCR7 in these disease states. Although some small molecules were initially reported as antagonists due to their displayed activity, many function as agonists while still producing the desired pharmacologic effects. A potential reason for this contradiction is that effects may be due to elevated extracellular CXCL12 levels.

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Cite this
GOST |
Cite this
GOST Copy
Lounsbury N. Advances in CXCR7 Modulators // Pharmaceuticals. 2020. Vol. 13. No. 2. p. 33.
GOST all authors (up to 50) Copy
Lounsbury N. Advances in CXCR7 Modulators // Pharmaceuticals. 2020. Vol. 13. No. 2. p. 33.
RIS |
Cite this
RIS Copy
TY - JOUR
DO - 10.3390/ph13020033
UR - https://doi.org/10.3390/ph13020033
TI - Advances in CXCR7 Modulators
T2 - Pharmaceuticals
AU - Lounsbury, Nicole
PY - 2020
DA - 2020/02/21
PB - MDPI
SP - 33
IS - 2
VL - 13
PMID - 32098047
SN - 1424-8247
ER -
BibTex |
Cite this
BibTex (up to 50 authors) Copy
@article{2020_Lounsbury,
author = {Nicole Lounsbury},
title = {Advances in CXCR7 Modulators},
journal = {Pharmaceuticals},
year = {2020},
volume = {13},
publisher = {MDPI},
month = {feb},
url = {https://doi.org/10.3390/ph13020033},
number = {2},
pages = {33},
doi = {10.3390/ph13020033}
}
MLA
Cite this
MLA Copy
Lounsbury, Nicole. “Advances in CXCR7 Modulators.” Pharmaceuticals, vol. 13, no. 2, Feb. 2020, p. 33. https://doi.org/10.3390/ph13020033.