Evidence map›Paper›PMID 18320069›Full record

ArticleNeoplasia (New York, N.Y.)2008

CXCL5 promotes prostate cancer progression.

Lesa A Begley, Sathish Kasina, Rohit Mehra, Shreelekha Adsule, Andrew J Admon, Robert J Lonigro, Arul M Chinnaiyan, Jill A Macoska

Open access · goldAbstract read
In one paragraph

Article in Neoplasia (New York, N.Y.), 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 92 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
92citing papers in PubMed, 2 pooled it
3.6field-weighted citation impact, top 7% 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

92 citing papers in PubMed, 2 syntheses or guidelines pooled it, 136 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Progress in Designing Cytokine Antagonist Antibodies for Cancer Therapy.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. MDA-9/Syntenin in the tumor and microenvironment defines prostate cancer bone metastasis.Proceedings of the National Academy of Sciences of the United States of America · 2023
    Article
  17. Review
  18. CC Chemokine Receptor 4 (CCR4) as a Possible New Target for Therapy.International journal of molecular sciences · 2022
    Review
  19. Article
  20. Article

32 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

8 authors at 2 institutions in 1 country.

Lesa A BegleyDepartment of Urology, University of Michigan, Ann Arbor, MI 48109-0944, USA.
Sathish Kasina
Rohit Mehra
Shreelekha Adsule
Andrew J Admon
Robert J Lonigro
Arul M Chinnaiyan
Jill A Macoska
University of Michigan–Ann Arbor · USMichigan Center for Translational Pathology · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Eric R. Fearon · 1988 to 2026
$178.2M
University of Michigan O'Brien Center for Urology ResearchP50DK065313 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SANDA, MARTIN G · 2003 to 2007
$3.3M
NCI NIH HHS 5 P30 CA46592NCI NIH HHS 5 P50 CA068568NCI NIH HHS P30 CA046592NIDDK NIH HHS P50 DK065313
6 · The paper itself

Abstract

CXCL5 is a proangiogenic CXC-type chemokine that is an inflammatory mediator and a powerful attractant for granulocytic immune cells. Unlike many other chemokines, CXCL5 is secreted by both immune (neutrophil, monocyte, and macrophage) and nonimmune (epithelial, endothelial, and fibroblastic) cell types. The current study was intended to determine which of these cell types express CXCL5 in normal and malignant human prostatic tissues, whether expression levels correlated with malignancy and whether CXCL5 stimulated biologic effects consistent with a benign or malignant prostate epithelial phenotype. The results of these studies show that CXCL5 protein expression levels are concordant with prostate tumor progression, are highly associated with inflammatory infiltrate, and are frequently detected in the lumens of both benign and malignant prostate glands. Exogenous administration of CXCL5 stimulates cellular proliferation and gene transcription in both nontransformed and transformed prostate epithelial cells and induces highly aggressive prostate cancer cells to invade through synthetic basement membrane in vitro. These findings suggest that the inflammatory mediator, CXCL5, may play multiple roles in the etiology of both benign and malignant proliferative diseases in the prostate.

Indexed as

Cell Line, TumorCell MovementCell ProliferationChemokine CXCL5Early Growth Response Protein 1HumansMaleMitogen-Activated Protein KinasesNeoplasm InvasivenessPhosphatidylinositol 3-KinasesProstatic NeoplasmsTissue Array AnalysisTranscription, GeneticChemokine CXCL5CXCL5 protein, humanEarly Growth Response Protein 1EGR1 protein, humanMitogen-Activated Protein KinasesPhosphatidylinositol 3-Kinases

Identifiers

PMID18320069
PMCPMC2262133
OpenAlexW1764421709

What Socratic holds

Textmetadata
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 Socratic graph.