Evidence map›Paper›PMID 32481745›Full record

ArticleInternational journal of molecular sciences2020

Cdc42-Dependent Transfer of mir301 from Breast Cancer-Derived Extracellular Vesicles Regulates the Matrix Modulating Ability of Astrocytes at the Blood-Brain Barrier.

Golnaz Morad, Cassandra C Daisy, Hasan H Otu, Towia A Libermann, Simon T Dillon, Marsha A Moses

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

26 citing papers in PubMed, 33 citations in OpenAlex.

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  9. The role of microRNAs in brain metastasis.Journal of neuro-oncology · 2024
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  18. Tumor-Derived Exosomes and Their Role in Breast Cancer Metastasis.International journal of molecular sciences · 2022
    Review
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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

6 authors at 3 institutions in 1 country.

Golnaz MoradVascular Biology Program, Boston Children's Hospital, Boston, 02115 MA, USA.ORCID 0000-0002-9460-618X
Cassandra C DaisyVascular Biology Program, Boston Children's Hospital, Boston, 02115 MA, USA.ORCID 0000-0001-5244-8067
Hasan H OtuDepartment of Electrical and Computer Engineering, University of Nebraska-Lincoln, Lincoln, NE 68588, USA.
Towia A LibermannBIDMC Genomics, Proteomics, Bioinformatics and Systems Biology Center, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA.
Simon T DillonBIDMC Genomics, Proteomics, Bioinformatics and Systems Biology Center, Beth Israel Deaconess Medical Center, Boston, MA 02115, USA.
Marsha A MosesVascular Biology Program, Boston Children's Hospital, Boston, 02115 MA, USA.
Boston Children's Hospital · USBeth Israel Deaconess Medical Center · USUniversity of Nebraska–Lincoln · US

Funding

(PQA2): Escape from breast tumor dormancy: convergence of obesity and menopauseR01CA185530 · NCI · BOSTON CHILDREN'S HOSPITAL · PI MOSES, MARSHA A · 2014 to 2017
$1.5M
Advanced Medical Research Foundation N/ABreast Cancer Research Foundation N/ANIH HHS R01 CA185530
6 · The paper itself

Abstract

Breast cancer brain metastasis is a major clinical challenge and is associated with a dismal prognosis. Understanding the mechanisms underlying the early stages of brain metastasis can provide opportunities to develop efficient diagnostics and therapeutics for this significant clinical challenge. We have previously reported that breast cancer-derived extracellular vesicles (EVs) breach the blood-brain barrier (BBB) via transcytosis and can promote brain metastasis. Here, we elucidate the functional consequences of EV transport across the BBB. We demonstrate that brain metastasis-promoting EVs can be internalized by astrocytes and modulate the behavior of these cells to promote extracellular matrix remodeling in vivo. We have identified protein and miRNA signatures in these EVs that can lead to the interaction of EVs with astrocytes and, as such, have the potential to serve as targets for development of diagnostics and therapeutics for early detection and therapeutic intervention in breast cancer brain metastasis.

Indexed as

Blood-Brain BarrierAnimalsAstrocytesBreast Neoplasmscdc42 GTP-Binding ProteinCell Line, TumorCluster AnalysisCulture Media, ConditionedEndocytosisExtracellular MatrixExtracellular VesiclesFemaleHumansMiceMice, NudeMicroRNAscdc42 GTP-Binding ProteinCDC42 protein, humanCdc42 protein, mouseCulture Media, ConditionedMicroRNAsMIRN301A microRNA, humanMIRN301 microRNA, mouseTIMP2 protein, humanTimp2 protein, mouseTissue Inhibitor of Metalloproteinase-2blood–brain barrierbrain metastasisbreast cancerextracellular vesiclesmicroRNA

Identifiers

PMID32481745
PMCPMC7311991
OpenAlexW3030159680

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.