Evidence map›Paper›PMID 29321662›Full record

ArticleOncogene2018

Breast cancer metastasis to liver and lung is facilitated by Pit-1-CXCL12-CXCR4 axis.

Anxo Martinez-Ordoñez, Samuel Seoane, Pablo Cabezas, Noemi Eiro, Juan Sendon-Lago, Manuel Macia, Tomas Garcia-Caballero, Luis O Gonzalez, Laura Sanchez, Francisco Vizoso and 1 more

Abstract read
PubMed Publisher
In one paragraph

Article in Oncogene, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.2field-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

49 citing papers in PubMed, 81 citations in OpenAlex.

  1. Article
  2. Article
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  4. Article
  5. Article
  6. The role of CXC chemokines and receptors in breast cancer.Clinical and experimental medicine · 2025
    Review
  7. Article
  8. ComparingCancers · 2025
    Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Review
  14. Review
  15. Article
  16. Article
  17. Article
  18. Review
  19. CXCL12-CXCR4/CXCR7 Axis in Cancer: from Mechanisms to Clinical Applications.International journal of biological sciences · 2023
    Review
  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

11 authors at 3 institutions in 1 country.

Anxo Martinez-OrdoñezDepartment of Physiology-Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), University of Santiago de Compostela, Santiago de Compostela, Spain.
Samuel SeoaneDepartment of Physiology-Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), University of Santiago de Compostela, Santiago de Compostela, Spain.
Pablo CabezasDepartment of Genetics, University of Santiago de Compostela, Campus de Lugo, Lugo, Spain.
Noemi EiroResearch Unit, Hospital Fundacion de Jove, Gijón, Spain.
Juan Sendon-LagoDepartment of Physiology-Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), University of Santiago de Compostela, Santiago de Compostela, Spain.
Manuel MaciaDepartment of Obstetrics and Gynecology, University of Santiago de Compostela, Santiago de Compostela, Spain.
Tomas Garcia-CaballeroDepartment of Morphological Sciences, University of Santiago de Compostela, Santiago de Compostela, Spain.
Luis O GonzalezResearch Unit, Hospital Fundacion de Jove, Gijón, Spain.
Laura SanchezDepartment of Genetics, University of Santiago de Compostela, Campus de Lugo, Lugo, Spain.
Francisco VizosoResearch Unit, Hospital Fundacion de Jove, Gijón, Spain.
Roman Perez-FernandezDepartment of Physiology-Center for Research in Molecular Medicine and Chronic Diseases (CIMUS), University of Santiago de Compostela, Santiago de Compostela, Spain. roman.perez.fernandez@usc.es.
Universidade de Santiago de Compostela · ESFundación Hospital de Jove · ESCenter for Research in Molecular Medicine and Chronic Diseases · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Development of human tumors is driven by accumulation of alterations in tumor suppressor genes and oncogenes in cells. The POU1F1 transcription factor (also known Pit-1) is expressed in the mammary gland and its overexpression induces profound phenotypic changes in proteins involved in breast cancer progression. Patients with breast cancer and elevated expression of Pit-1 show a positive correlation with the occurrence of distant metastasis and poor overall survival. However, some mediators of Pit-1 actions are still unknown. Here, we show that CXCR4 chemokine receptor and its ligand CXCL12 play a critical role in the pro-tumoral process induced by Pit-1. We found that Pit-1 increases mRNA and protein in both CXCR4 and CXCL12. Knock-down of CXCR4 reduces tumor growth and spread of Pit-1 overexpressing cells in a zebrafish xenograft model. Furthermore, we described for the first time pro-angiogenic effects of Pit-1 through the CXCL12-CXCR4 axis, and that extravasation of Pit-1 overexpressing breast cancer cells is strongly reduced in CXCL12-deprived target tissues. Finally, in breast cancer patients, expression of Pit-1 in primary tumors was found to be positively correlated with CXCR4 and CXCL12, with specific metastasis in liver and lung, and with clinical outcome. Our results suggest that Pit-1-CXCL12-CXCR4 axis could be involved in chemotaxis guidance during the metastatic process, and may represent prognostic and/or therapeutic targets in breast tumors.

Indexed as

AnimalsBreast NeoplasmsCell MovementCell ProliferationCells, CulturedChemokine CXCL12Embryo, NonmammalianFemaleGene Expression Regulation, NeoplasticHumansHuman Umbilical Vein Endothelial CellsLiver NeoplasmsLung NeoplasmsMCF-7 CellsNeoplasm InvasivenessNeovascularization, PathologicChemokine CXCL12CXCL12 protein, humanCXCR4 protein, humanPOU1F1 protein, humanReceptors, CXCR4Transcription Factor Pit-1

Identifiers

PMID29321662
OpenAlexW2782830014

What OpenQuestion 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 OpenQuestion graph.