Evidence map›Paper›PMID 28008153›Full record

ArticleOncotarget2017

PTEN mediates the cross talk between breast and glial cells in brain metastases leading to rapid disease progression.

Ina Hohensee, Han-Ning Chuang, Astrid Grottke, Stefan Werner, Alexander Schulte, Stefan Horn, Katrin Lamszus, Kai Bartkowiak, Isabell Witzel, Manfred Westphal and 6 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
3.1field-weighted citation impact, top 8% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 42 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Biological profile of breast cancer brain metastasis.Acta neuropathologica communications · 2025
    Review
  4. Article
  5. Article
  6. Organ-Specificity of Breast Cancer Metastasis.International journal of molecular sciences · 2023
    Review
  7. Article
  8. Article
  9. Article
  10. An Insight into Molecular Targets of Breast Cancer Brain Metastasis.International journal of molecular sciences · 2022
    Review
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
  17. Review
  18. Review
  19. Article
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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

16 authors at 4 institutions in 1 country.

Ina HohenseeInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.
Han-Ning ChuangDepartment of Hematology/Oncology, University Medical Center Göttingen, 37099 Göttingen, Germany.
Astrid GrottkeInstitute of Biochemistry and Signal Transduction, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Stefan WernerInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.
Alexander SchulteDepartment of Neurosurgery, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Stefan HornBone Marrow Transplantation Unit, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Katrin LamszusDepartment of Neurosurgery, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Kai BartkowiakInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.
Isabell WitzelDepartment of Gynecology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Manfred WestphalDepartment of Neurosurgery, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Jakob MatschkeInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg-Eppendorf, 20246 Hamburg, Germany.
Markus GlatzelInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg-Eppendorf, 20246 Hamburg, Germany.
Manfred JückerInstitute of Biochemistry and Signal Transduction, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Tobias PukropDepartment of Hematology/Oncology, University Medical Center Göttingen, 37099 Göttingen, Germany.
Klaus PantelInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.
Harriet WikmanInstitute of Tumor Biology, University Medical Center Hamburg-Eppendorf, Hamburg, 20246, Germany.
Universität Hamburg · DEUniversity Medical Center Hamburg-Eppendorf · DEUniversitätsmedizin Göttingen · DEUniversity Hospital Regensburg · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite improvement of therapeutic treatments for breast cancer, the development of brain metastases has become a major limitation to life expectancy for many patients. Brain metastases show very commonly alterations in EGFR and HER2 driven pathways, of which PTEN is an important regulator. Here, we analyzed PTEN expression in 111 tissue samples of breast cancer brain metastases (BCBM). Loss of PTEN was found in a substantial proportion of BCBM samples (48.6%) and was significantly associated with triple-negative breast cancer (67.5%, p = 0.001) and a shorter survival time after surgical resection of brain metastases (p = 0.048). Overexpression of PTEN in brain-seeking MDA-MB-231 BR cells in vitro reduced activation of the AKT pathway, notably by suppression of Akt1 kinase activity. Furthermore, the migration of MDA-MB-231 BR cells in vitro was promoted by co-culturing with both astrocytes and microglial cells. Interestingly, when PTEN was overexpressed the migration was significantly inhibited. Moreover, in an ex vivo organotypic brain slice model, PTEN overexpression reduced invasion of tumor cells. This was accompanied by reduced astrocyte activation that was mediated by autocrine and paracrine activation of GM-CSF/ CSF2RA and AKT/ PTEN pathways. In conclusion, loss of PTEN is frequently detected in triple-negative BCBM patients and associated with poor prognosis. The findings of our functional studies suggest that PTEN loss promotes a feedback loop between tumor cells and glial cells, which might contribute to disease progression.

Indexed as

Brain NeoplasmsCell Line, TumorCell MovementCell ProliferationCoculture TechniquesDisease ProgressionFeedback, PhysiologicalFemaleGene Expression Regulation, NeoplasticHumansNeoplasm InvasivenessNeurogliaProto-Oncogene Proteins c-aktPTEN PhosphohydrolaseSurvival AnalysisTriple Negative Breast NeoplasmsAKT1 protein, humanProto-Oncogene Proteins c-aktPTEN PhosphohydrolasePTEN protein, humanastrocytesbrain metastasesbreast cancermicroenvironmentPTEN

Identifiers

PMID28008153
PMCPMC5351620
OpenAlexW2566138113

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.