Evidence map›Paper›PMID 31562303›Full record

ArticleNature communications2019

The CXCL5/CXCR2 axis is sufficient to promote breast cancer colonization during bone metastasis.

Ricardo Romero-Moreno, Kimberly J Curtis, Thomas R Coughlin, Maria Cristina Miranda-Vergara, Shourik Dutta, Aishwarya Natarajan, Beth A Facchine, Kristen M Jackson, Lukas Nystrom, Jun Li and 3 more

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 105 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
105citing papers in PubMed, 2 pooled it
7.3field-weighted citation impact, top 2% 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

105 citing papers in PubMed, 2 syntheses or guidelines pooled it, 143 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Review
  11. Mechanisms of breast cancer dormancy in bone metastasis.Clinical & experimental metastasis · 2026
    Review
  12. Article
  13. Article
  14. Article
  15. Metabolism in Tumour-Induced Bone Disease.Current osteoporosis reports · 2026
    Review
  16. Review
  17. Article
  18. Review
  19. CXCL2/CXCR2 pathway regulates CD169Frontiers in medicine · 2026
    Article
  20. Article

45 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 3 institutions in 1 country.

Ricardo Romero-MorenoHarper Cancer Research Institute, South Bend, IN, USA.
Kimberly J CurtisHarper Cancer Research Institute, South Bend, IN, USA.
Thomas R CoughlinHarper Cancer Research Institute, South Bend, IN, USA.
Maria Cristina Miranda-VergaraHarper Cancer Research Institute, South Bend, IN, USA.
Shourik DuttaHarper Cancer Research Institute, South Bend, IN, USA.
Aishwarya NatarajanHarper Cancer Research Institute, South Bend, IN, USA.
Beth A FacchineHarper Cancer Research Institute, South Bend, IN, USA.
Kristen M JacksonHarper Cancer Research Institute, South Bend, IN, USA.
Lukas NystromDepartment of Orthopaedic Surgery and Rehabilitation, Loyola University Medical Center, Stritch School of Medicine, Maywood, IL, USA.
Jun LiHarper Cancer Research Institute, South Bend, IN, USA.
William KalineyHarper Cancer Research Institute, South Bend, IN, USA.
Glen L NieburHarper Cancer Research Institute, South Bend, IN, USA.ORCID http://orcid.org/0000-0002-7134-2716
Laurie E LittlepageHarper Cancer Research Institute, South Bend, IN, USA. laurie.littlepage@nd.edu.ORCID http://orcid.org/0000-0002-0839-8274
University of Notre Dame · USLoyola University Medical Center · USMike and Josie Harper Cancer Research Institute

Funding

Online Raman Diagnostics of OncometabolitesR33CA206922 · NCI · UNIVERSITY OF NOTRE DAME · PI SCHULTZ, ZACHARY · 2016 to 2018
$1.0M
Statistical analysis of single cell RNA-sequencing data: detecting dropouts and removing the cell-cycle effectR03CA212964 · NCI · UNIVERSITY OF NOTRE DAME · PI LI, JUN · 2017 to 2018
$155k
NCI NIH HHS R03 CA212964NCI NIH HHS R33 CA206922
6 · The paper itself

Abstract

Bone is one of the most common sites for metastasis across cancers. Cancer cells that travel through the vasculature and invade new tissues can remain in a non-proliferative dormant state for years before colonizing the metastatic site. Switching from dormancy to colonization is the rate-limiting step of bone metastasis. Here we develop an ex vivo co-culture method to grow cancer cells in mouse bones to assess cancer cell proliferation using healthy or cancer-primed bones. Profiling soluble factors from conditioned media identifies the chemokine CXCL5 as a candidate to induce metastatic colonization. Additional studies using CXCL5 recombinant protein suggest that CXCL5 is sufficient to promote breast cancer cell proliferation and colonization in bone, while inhibition of its receptor CXCR2 with an antagonist blocks proliferation of metastatic cancer cells. This study suggests that CXCL5 and CXCR2 inhibitors may have efficacy in treating metastatic bone tumors dependent on the CXCL5/CXCR2 axis.

Indexed as

AnimalsBone NeoplasmsBreast NeoplasmsCell Line, TumorCell MovementCell ProliferationChemokine CXCL5Epithelial-Mesenchymal TransitionFemaleHumansMice, TransgenicMiddle AgedPhenylurea CompoundsReceptors, Interleukin-8BSignal TransductionChemokine CXCL5Phenylurea CompoundsReceptors, Interleukin-8BSB 225002

Identifiers

PMID31562303
PMCPMC6765048
OpenAlexW2976432085

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.