Evidence map›Paper›PMID 39448577›Full record

ArticleNature communications2024

Osteopontin is a therapeutic target that drives breast cancer recurrence.

Yu Gu, Tarek Taifour, Tung Bui, Dongmei Zuo, Alain Pacis, Alexandre Poirier, Sherif Attalla, Anne-Marie Fortier, Virginie Sanguin-Gendreau, Tien-Chi Pan and 9 more

Abstract read
In one paragraph

Article in Nature communications, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

34 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Gender-Dependent Differences in Serum Osteopontin Levels in Chronic Spontaneous Urticaria: A Link to Disease Activity in Females.Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology · 2026
    Article
  3. Context-dependent roles of osteopontin in aging-related neurological disorders.The Journal of international medical research · 2026
    Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Multiregional profiling revealsScience advances · 2026
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  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

19 authors.

Yu GuRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.
Tarek TaifourRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.
Tung BuiRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.
Dongmei ZuoRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.
Alain PacisRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.
Alexandre PoirierRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.ORCID 0000-0002-6754-6003
Sherif AttallaRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.
Anne-Marie FortierRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.ORCID 0000-0002-0428-3066
Virginie Sanguin-GendreauRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.
Tien-Chi PanDepartment of Cancer Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Vasilios PapavasiliouRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.
Nancy U LinDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0003-2263-5413
Melissa E HughesDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Kalie SmithDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.
Morag ParkRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.ORCID 0000-0001-5400-606X
Michel L TremblayRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada.ORCID 0000-0002-0281-541X
Lewis A ChodoshDepartment of Cancer Biology, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
Rinath JeselsohnDepartment of Medical Oncology, Dana-Farber Cancer Institute, Boston, MA, USA.ORCID 0000-0001-7996-7529
William J MullerRosalind and Morris Goodman Cancer Institute, McGill University, Montreal, QC, Canada. william.muller@mcgill.ca.ORCID 0000-0002-7293-4166

Funding

Canadian Cancer Society Research Institute (Société Canadienne du Cancer) 706216Canadian Cancer Society Research Institute (Société Canadienne du Cancer) 706679Canadian Cancer Society Research Institute (Société Canadienne du Cancer) 708195Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) 187660Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) FDN-148373Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada) PLL - 190347
6 · The paper itself

Abstract

Recurrent breast cancers often develop resistance to standard-of-care therapies. Identifying targetable factors contributing to cancer recurrence remains the rate-limiting step in improving long-term outcomes. In this study, we identify tumor cell-derived osteopontin as an autocrine and paracrine driver of tumor recurrence. Osteopontin promotes tumor cell proliferation, recruits macrophages, and synergizes with IL-4 to further polarize them into a pro-tumorigenic state. Macrophage depletion and osteopontin inhibition decrease recurrent tumor growth. Furthermore, targeting osteopontin in primary tumor-bearing female mice prevents metastasis, permits T cell infiltration and activation, and improves anti-PD-1 immunotherapy response. Clinically, osteopontin expression is higher in recurrent metastatic tumors versus female patient-matched primary breast tumors. Osteopontin positively correlates with macrophage infiltration, increases with higher tumor grade, and its elevated pathway activity is associated with poor prognosis and long-term recurrence. Our findings suggest clinical implications and an alternative therapeutic strategy based on osteopontin's multiaxial role in breast cancer progression and recurrence.

Indexed as

Breast NeoplasmsCell ProliferationNeoplasm Recurrence, LocalOsteopontinAnimalsCell Line, TumorFemaleGene Expression Regulation, NeoplasticHumansInterleukin-4MacrophagesMicePrognosisInterleukin-4OsteopontinSPP1 protein, human

Identifiers

PMID39448577
PMCPMC11502809

What OpenQuestion holds

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Registered trials

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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.