Evidence map›Paper›PMID 23720051›Full record

ArticleCancer research2013

CX3CL1 promotes breast cancer via transactivation of the EGF pathway.

Manuel Tardáguila, Emilia Mira, Miguel A García-Cabezas, Anna M Feijoo, Miguel Quintela-Fandino, Iñigo Azcoitia, Sergio A Lira, Santos Mañes

Abstract read
In one paragraph

Article in Cancer research, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

56 citing papers in PubMed, 98 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. CX3CR1Cancer science · 2024
    Review
  7. Fractalkine in Health and Disease.International journal of molecular sciences · 2024
    Review
  8. Review
  9. Review
  10. Alterations in CX3CL1 Levels and Its Role in Viral Pathogenesis.International journal of molecular sciences · 2024
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Fractalkine Signalling (CXJournal of clinical medicine · 2023
    Review
  18. Article
  19. Article
  20. Article
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 3 institutions in 2 countries.

Manuel TardáguilaDepartment of Immunology and Oncology, Centro Nacional de Biotecnología/CSIC, Madrid, Spain.
Emilia Mira
Miguel A García-Cabezas
Anna M Feijoo
Miguel Quintela-Fandino
Iñigo Azcoitia
Sergio A Lira
Santos Mañes
Icahn School of Medicine at Mount Sinai · USCentro Nacional de Biotecnología · ESUniversidad Complutense de Madrid · ES

Funding

Molecular pathogenesis of intestinal serrated polypsR01CA161373 · NCI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI LIRA, SERGIO A. · 2011 to 2020
$3.7M
NCI NIH HHS R01 CA161373
6 · The paper itself

Abstract

Chemokines are relevant molecules in shaping the tumor microenvironment, although their contributions to tumorigenesis are not fully understood. We studied the influence of the chemokine CX3CL1/fractalkine in de novo breast cancer formation using HER2/neu transgenic mice. CX3CL1 expression was downmodulated in HER2/neu tumors, yet, paradoxically, adenovirus-mediated CX3CL1 expression in the tumor milieu enhanced mammary tumor numbers in a dose-dependent manner. Increased tumor multiplicity was not a consequence of CX3CL1-induced metastatic dissemination of the primary tumor, although CX3CL1 induced epithelial-to-mesenchymal transition in breast cancer cells in vitro. Instead, CX3CL1 triggered cell proliferation by induction of ErbB receptors through the proteolytic shedding of an ErbB ligand. This effect was important insofar as mammary tumorigenesis was delayed and tumor multiplicity was reduced by genetic deletion of CX3CL1 in HER2/neu mice, but not in polyoma middle T-antigen oncomice. Our findings support the conclusion that CX3CL1 acts as a positive modifier of breast cancer in concert with ErbB receptors.

Indexed as

Transcriptional ActivationAnimalsBreast NeoplasmsCarcinogenesisCell Line, TumorCell ProliferationChemokine CX3CL1Epidermal Growth FactorEpithelial-Mesenchymal TransitionErb-b2 Receptor Tyrosine KinasesFemaleHumansLymphatic MetastasisLymph NodesMammary Glands, AnimalMammary Neoplasms, AnimalChemokine CX3CL1Epidermal Growth FactorErb-b2 Receptor Tyrosine KinasesReceptors, Chemokine

Identifiers

PMID23720051
PMCPMC4533861
OpenAlexW2081777966

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.