Evidence map›Paper›PMID 19690611›Full record

ArticlePloS one2009

The chemokine CXCL16 and its receptor, CXCR6, as markers and promoters of inflammation-associated cancers.

Merav Darash-Yahana, John W Gillespie, Stephen M Hewitt, Yun-Yun K Chen, Shin Maeda, Ilan Stein, Satya P Singh, Roble B Bedolla, Amnon Peled, Dean A Troyer and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
4.7field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

75 citing papers in PubMed, 142 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. A distinct population of CD8Nature aging · 2025
    Article
  8. Article
  9. Chemokines that govern T cell activity in tumors.Current opinion in immunology · 2025
    Review
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Inflammation in Urological Malignancies: The Silent Killer.International journal of molecular sciences · 2023
    Review
  19. Article
  20. Article

15 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 6 institutions in 3 countries.

Merav Darash-YahanaLaboratory of Molecular Immunology, National Institute of Allergy and Infectious Diseases (NIAID), National Institutes of Health (NIH), Bethesda, MD, USA. meravd@hadassah.org.il
John W Gillespie
Stephen M Hewitt
Yun-Yun K Chen
Shin Maeda
Ilan Stein
Satya P Singh
Roble B Bedolla
Amnon Peled
Dean A Troyer
Eli Pikarsky
Michael Karin
Joshua M Farber
Hadassah Medical Center · ILNational Institute of Allergy and Infectious Diseases · USNational Cancer Institute · USThe University of Texas Health Science Center at San Antonio · USInstitute for Adult Diseases Asahi Life Foundation · JPUniversity of California, San Diego · US

Funding

Tissue Array Research ProgramZICBC010923 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI HEWITT, STEPHEN · 2009 to 2014
$4.7M
Characterization Of Novel Chemokine Receptors In LymphocytesZIAAI000749 · NIAID · NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES · PI FARBER, JOSHUA M · 2009 to 2011
$4.0M
CHARACTERIZATION OF NOVEL CHEMOKINE RECEPTORS IN LYMPHOCYTESZ01AI000749 · NIAID · NIAID EXTRAMURAL ACTIVITIES · PI FARBER, JOSHUA M · 1996 to 2008
$1.1M
Intramural NIH HHS
6 · The paper itself

Abstract

Clinical observations and mouse models have suggested that inflammation can be pro-tumorigenic. Since chemokines are critical in leukocyte trafficking, we hypothesized that chemokines play essential roles in inflammation-associated cancers. Screening for 37 chemokines in prostate cancer cell lines and xenografts revealed CXCL16, the ligand for the receptor CXCR6, as the most consistently expressed chemokine. Immunohistochemistry and/or immunofluorescence and confocal imaging of 121 human prostate specimens showed that CXCL16 and CXCR6 were co-expressed, both on prostate cancer cells and adjacent T cells. Expression levels of CXCL16 and CXCR6 on cancer cells correlated with poor prognostic features including high-stage and high-grade, and expression also correlated with post-inflammatory changes in the cancer stroma as revealed by loss of alpha-smooth muscle actin. Moreover, CXCL16 enhanced the growth of CXCR6-expressing cancer and primary CD4 T cells. We studied expression of CXCL16 in an additional 461 specimens covering 12 tumor types, and found that CXCL16 was expressed in multiple human cancers associated with inflammation. Our study is the first to describe the expression of CXCL16/CXCR6 on both cancer cells and adjacent T cells in humans, and to demonstrate correlations between CXCL16 and CXCR6 vs. poor both prognostic features and reactive changes in cancer stoma. Taken together, our data suggest that CXCL16 and CXCR6 may mark cancers arising in an inflammatory milieu and mediate pro-tumorigenic effects of inflammation through direct effects on cancer cell growth and by inducing the migration and proliferation of tumor-associated leukocytes.

Indexed as

Biomarkers, TumorCD4-Positive T-LymphocytesChemokine CXCL16Chemokines, CXCEnzyme-Linked Immunosorbent AssayHumansImmunohistochemistryInflammationMaleProstatic NeoplasmsReceptors, ChemokineReceptors, CXCR6Receptors, ScavengerReceptors, VirusReverse Transcriptase Polymerase Chain ReactionBiomarkers, TumorChemokine CXCL16Chemokines, CXCCXCL16 protein, humanCXCR6 protein, humanReceptors, ChemokineReceptors, CXCR6Receptors, ScavengerReceptors, Virus

Identifiers

PMID19690611
PMCPMC2723911
OpenAlexW2093728029

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.