Evidence map›Paper›PMID 19544560›Full record

ArticleInternational journal of cancer2009

Antagonism of chemokine receptor CXCR3 inhibits osteosarcoma metastasis to lungs.

Emmanuelle Pradelli, Babou Karimdjee-Soilihi, Jean-François Michiels, Jean-Ehrland Ricci, Marie-Ange Millet, Fanny Vandenbos, Timothy J Sullivan, Tassie L Collins, Michael G Johnson, Julio C Medina and 3 more

Open access · greenAbstract read
In one paragraph

Article in International journal of cancer, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 64 papers.

0numbers the graph read from it
0cells of the map it votes in
64citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

64 citing papers in PubMed, 110 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. The role of CXC chemokines and receptors in breast cancer.Clinical and experimental medicine · 2025
    Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Targeting CXCL9/10/11-CXCR3 axis: an important component of tumor-promoting and antitumor immunity.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Review
  18. Extracellular Vesicles in Osteosarcoma: Antagonists or Therapeutic Agents?International journal of molecular sciences · 2021
    Review
  19. Review
  20. Article

4 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 2 countries.

Emmanuelle PradelliUniversité de Nice Sophia-Antipolis, Nice, France.
Babou Karimdjee-Soilihi
Jean-François Michiels
Jean-Ehrland Ricci
Marie-Ange Millet
Fanny Vandenbos
Timothy J Sullivan
Tassie L Collins
Michael G Johnson
Julio C Medina
Eugenie S Kleinerman
Annie Schmid-Alliana
Heidy Schmid-Antomarchi
Amgen (United States) · USInserm · FRUniversité Côte d'Azur · FRHôpital l'Archet · FRHôpital Pasteur · FRThe University of Texas MD Anderson Cancer Center · US

Funding

LIPOSOME THERAPY--A POTENTIAL ADJUVANT FOR OSTEOSARCOMAR01CA042992 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KLEINERMAN, EUGENIE S · 1986 to 2010
$3.3M
NCI NIH HHS R01 CA042992
6 · The paper itself

Abstract

Metastasis continues to be the leading cause of mortality for patients with cancer. Several years ago, it became clear that chemokines and their receptors could control the tumor progress. CXCR3 has now been identified in many cancers including osteosarcoma and CXCR3 ligands were expressed by lungs that are the primary sites to which this tumor metastasize. This study tested the hypothesis that disruption of the CXCR3/CXCR3 ligands complexes could lead to a decrease in lungs metastasis. The experimental design involved the use of the CXCR3 antagonist, AMG487 and 2 murine models of osteosarcoma lung metastases. After tail vein injection of osteosarcoma cells, mice that were systematically treated with AMG487 according to preventive or curative protocols had a significant reduction in metastatic disease. Treatment of osteosarcoma cells in vitro with AMG487 led to decreased migration, decreased matrix metalloproteinase activity, decreased proliferation/survival and increased caspase-independent death. Taken together, our results support the hypothesis that CXCR3 and their ligands intervene in the initial dissemination of the osteosarcoma cells to the lungs and stimulate the growth and expansion of the metastatic foci in later stages. Moreover, these studies indicate that targeting CXCR3 may specifically inhibit tumor metastasis without adversely affecting antitumoral host response.

Indexed as

AcetamidesAnimalsApoptosisBlotting, WesternCalciumCaspasesCell MovementFemaleHumansLung NeoplasmsMiceMice, Inbred BALB CMice, NudeNeoplasm InvasivenessOsteosarcomaPyrimidinonesAcetamidesCalciumCaspasesCXCR3 protein, humanCxcr3 protein, mouseN-(1-(3-(4-ethoxyphenyl)-4-oxo-3,4-dihydropyrido(2,3-d)pyrimidin-2-yl)ethyl)-N-pyridin-3-ylmethyl-2-(4-trifluoromethoxyphenyl)acetamidePyrimidinonesReceptors, CXCR3

Identifiers

PMID19544560
PMCPMC2772145
OpenAlexW1964613018

What OpenQuestion holds

Textmetadata
LicenceTDM
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.