Evidence map›Paper›PMID 32534480›Full record

ArticleMolecular oncology2020

Pericyte-secreted IGF2 promotes breast cancer brain metastasis formation.

Kinga Molnár, Ádám Mészáros, Csilla Fazakas, Mihály Kozma, Fanni Győri, Zita Reisz, László Tiszlavicz, Attila E Farkas, Ádám Nyúl-Tóth, János Haskó and 2 more

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed, 1 pooled it
2.4field-weighted citation impact, top 9% 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

39 citing papers in PubMed, 1 synthesis or guideline pooled it, 47 citations in OpenAlex.

  1. Pooled it
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  12. Eppur si muove: the dynamic brain pericyte.Fluids and barriers of the CNS · 2025
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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

12 authors at 2 institutions in 3 countries.

Kinga MolnárInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.
Ádám MészárosInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.
Csilla FazakasInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.
Mihály KozmaInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.
Fanni GyőriInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.
Zita ReiszDepartment of Pathology, University of Szeged, Szeged, Hungary.
László TiszlaviczDepartment of Pathology, University of Szeged, Szeged, Hungary.
Attila E FarkasInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.
Ádám Nyúl-TóthInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.
János HaskóInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.
István A KrizbaiInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.
Imola WilhelmInstitute of Biophysics, Biological Research Centre, Szeged, Hungary.ORCID 0000-0003-2366-7337
University of Szeged · HUHUN-REN Szegedi Biológiai Kutatóközpont · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain metastases are life-threatening complications of triple-negative breast cancer, melanoma, and a few other tumor types. Poor outcome of cerebral secondary tumors largely depends on the microenvironment formed by cells of the neurovascular unit, among which pericytes are the least characterized. By using in vivo and in vitro techniques and human samples, here we show that pericytes play crucial role in the development of metastatic brain tumors by directly influencing key steps of the development of the disease. Brain pericytes had a prompt chemoattractant effect on breast cancer cells and established direct contacts with them. By secreting high amounts of extracellular matrix proteins, pericytes enhanced adhesion of both melanoma and triple-negative cancer cells, which might be particularly important in the exclusive perivascular growth of these tumor cells. In addition, pericytes secreted insulin-like growth factor 2 (IGF2), which had a very significant pro-proliferative effect on mammary carcinoma, but not on melanoma cells. By inhibiting IGF2 signaling using silencing or picropodophyllin (PPP), we could block the proliferation-increasing effect of pericytes on breast cancer cells. Administration of PPP (a blood-brain barrier-permeable substance) significantly decreased the size of brain tumors in mice inoculated with triple-negative breast cancer cells. Taken together, our results indicate that brain pericytes have significant pro-metastatic features, especially in breast cancer. Our study underlines the importance of targeting pericytes and the IGF axis as potential strategies in brain metastatic diseases.

Indexed as

AnimalsBrainBrain NeoplasmsBreast NeoplasmsCell AdhesionCell CommunicationCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHumansInsulin-Like Growth Factor IIMicePericytesRNA, MessengerIGF2 protein, humanInsulin-Like Growth Factor IIRNA, Messengerbrain metastasiscerebral pericyteinsulin-like growth factor 2picropodophyllintriple-negative breast cancer

Identifiers

PMID32534480
PMCPMC7463359
OpenAlexW3034643270

What OpenQuestion holds

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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.