Cited by 352Chemokine receptors and signalingAngiogenesis and VEGF in CancerImmune cells in cancer

Chemokines in cancer

Vicari, Alain P, Caux, Christophe·2002·Cytokine & Growth Factor Reviews

Abstract

Chemokines participate, by regulating cell trafficking and controlling angiogenesis, in the host response during infection and inflammation. Most of these mechanisms are also operating in cancer. The stimulation of angiogenesis and tumor growth--directly or indirectly through the recruitment of tumor-associated macrophages--are typical situations where chemokines promote tumor development. On the other hand, chemokines could be used to the benefit of cancer patients as they act in the recruitment of dendritic cells (DC) or/and effector cells or for their angiostatic properties. However, chemokine-mediated recruitment of immature DC within tumors, due to factors produced by the tumor milieu, could lead to the induction of immune tolerance and, therefore, novel strategies to eradicate tumors based on chemokines should attempt to avoid this risk.

Integrity signals

Registry

Crossref · 10.1016/s1359-6101(01)00033-8

Cites

164 of 164 references verified0 citation errors · 0 not checkable

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Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Other CXCR2 ligands have autocrine roles in the growth of pancreatic, head and neck, and non-small-cell lung carcinoma.

    “Other CXCR2 ligands have been identified as having autocrine roles in the growth of pancreatic, head and neck, and non-small-cell lung carcinoma44,45”

    From Inflammation and cancer (2002) · cites this paper as [44]

  • ELR+ CXC chemokines are pro-angiogenic and stimulate endothelial cell chemotaxis.

    “It is well established that CXC chemokines with the three amino acids (Glu-Leu-Arg/ELR) immediately amino-terminal to the CXC motif (ELR+) are pro-angiogenic and stimulate endothelial cell chemotaxis”

    From Inflammation and cancer (2002) · cites this paper as [44]

  • ELR− CXC chemokines possess angiostatic activities.

    “whereas ELR− CXC chemokines (for example, PF-4/CXCL4, MIG/CXCL9 and IP-10/CXCL10) possess angiostatic activities44,49.”

    From Inflammation and cancer (2002) · cites this paper as [44]

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Authors
Vicari, A. P., & Caux, C.
Corresponding author
Vicari, Alain P
Venue
Cytokine & Growth Factor Reviews
Publisher
Elsevier BV
Published
2002-04
Volume
13
Issue
2
Pages
143-154
ISSN
1359-6101 (ISSN-L)
OpenAlex
W2092021793
Cited by
351
References
173
Citations by year
2025: 2 · 2024: 4 · 2023: 3 · 2022: 4 · 2021: 9 · 2020: 14 · 2019: 11 · 2018: 9 · 2017: 13 · 2016: 12 · 2015: 16 · 2014: 20 · 2013: 18 · 2012: 21
FWCI
2.30
Type
journal article
Language
en
Open access
closed
Locations
  • Cytokine & Growth Factor Reviews (publishedVersion)
  • PubMed (publishedVersion)
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 › Immunology and Microbiology › Immunology › Immune cells in cancer
Keywords
chemokines, cancer, angiogenesis, tumor growth, tumor-associated macrophages, dendritic cell recruitment, immune tolerance, tumor microenvironment, cell trafficking
MeSH terms
Animals, Dendritic Cells, Humans, Killer Cells, Natural, Leukocytes, Models, Biological, Neoplasm Metastasis, Neoplasms, Neovascularization, Pathologic, T-Lymphocytes, Chemokines

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