Evidence map›Paper›PMID 29529015›Full record

ArticleNature medicine2018

Microenvironmental control of breast cancer subtype elicited through paracrine platelet-derived growth factor-CC signaling.

Pernilla Roswall, Matteo Bocci, Michael Bartoschek, Hong Li, Glen Kristiansen, Sara Jansson, Sophie Lehn, Jonas Sjölund, Steven Reid, Christer Larsson and 17 more

Registry-linked trialAbstract read
In one paragraph

Article in Nature medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05722795 (Use of Imatinib to Convert Triple Negative Breast Cancer Into ER-positive Breast Cancer), which is not on this map. Cited by 102 papers.

0numbers the graph read from it
0cells of the map it votes in
102citing papers in PubMed
–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.

NCT05722795 narecruitingnot on this mapstarted 2023, after this paper: background citation

Use of Imatinib to Convert Triple Negative Breast Cancer Into ER-positive Breast Cancer

TypeinterventionalSponsorVastra Gotaland RegionRan2023 to 2029Enrolled40ConditionsBreast Cancer, Triple Negative Breast CancerArmsImatinib 400 MG Oral Tablet
3 · Its place in the literature

Who cites it

102 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. Article
  5. Cytokines and cancer-associated fibroblasts.Journal of hematology & oncology · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. Article
  19. Activation of Bivalent Gene POU4F1 Promotes and Maintains Basal-like Breast Cancer.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    Article
  20. Review

42 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors.

Pernilla RoswallDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Matteo BocciDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Michael BartoschekDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Hong LiDivision of Vascular Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Glen KristiansenInstitute of Pathology, University Hospital Bonn, Bonn, Germany.
Sara JanssonDivision of Oncology and Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.
Sophie LehnDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Jonas SjölundDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Steven ReidDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Christer LarssonDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Pontus ErikssonDivision of Oncology and Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.
Charlotte AnderbergDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Eliane CortezDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Lao H SaalDivision of Oncology and Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.ORCID 0000-0002-0815-1896
Christina Orsmark-PietrasDivision of Clinical Genetics, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Eugenia CorderoDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.
Bengt Kristian HallerDivision of Vascular Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.
Jari HäkkinenDivision of Oncology and Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.ORCID 0000-0002-8466-9179
Ingrid J G BurvenichOlivia Newton-John Cancer Research Institute and School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.
Elgene LimGarvan Institute of Medical Research, Sydney, New South Wales, Australia.
Akira OrimoDepartment of Pathology and Oncology, Juntendo University School of Medicine, Tokyo, Japan.
Mattias HöglundDivision of Oncology and Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.
Lisa RydénDivision of Oncology and Pathology, Department of Clinical Sciences, Lund University, Lund, Sweden.
Holger MochDepartment of Pathology and Molecular Pathology, University Hospital Zürich, Zürich, Switzerland.
Andrew M ScottOlivia Newton-John Cancer Research Institute and School of Cancer Medicine, La Trobe University, Melbourne, Victoria, Australia.
Ulf ErikssonDivision of Vascular Biology, Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Stockholm, Sweden.ORCID 0000-0002-4439-3980
Kristian PietrasDivision of Translational Cancer Research, Department of Laboratory Medicine, Lund University, Lund, Sweden.

Funding

European Research Council 309322
6 · The paper itself

Abstract

Breast tumors of the basal-like, hormone receptor-negative subtype remain an unmet clinical challenge, as there is high rate of recurrence and poor survival in patients following treatment. Coevolution of the malignant mammary epithelium and its underlying stroma instigates cancer-associated fibroblasts (CAFs) to support most, if not all, hallmarks of cancer progression. Here we delineate a previously unappreciated role for CAFs as determinants of the molecular subtype of breast cancer. We identified paracrine crosstalk between cancer cells expressing platelet-derived growth factor (PDGF)-CC and CAFs expressing the cognate receptors in human basal-like mammary carcinomas. Genetic or pharmacological intervention of PDGF-CC activity in mouse models of cancer resulted in conversion of basal-like breast cancers into a hormone receptor-positive state that enhanced sensitivity to endocrine therapy in previously resistant tumors. We conclude that specification of breast cancer to the basal-like subtype is under microenvironmental control and is therapeutically actionable.

Indexed as

Paracrine CommunicationTumor MicroenvironmentAnimalsBiomarkers, TumorBreast NeoplasmsCancer-Associated FibroblastsCell Line, TumorCell ProliferationEpithelial CellsEstrogen Receptor alphaFemaleFibrosisHumansLymphokinesMice, Inbred C57BLMiddle AgedBiomarkers, TumorEstrogen Receptor alphaLymphokinesPlatelet-Derived Growth Factorplatelet-derived growth factor C

Identifiers

PMID29529015
PMCPMC5896729

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Registered trials

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.