Evidence map›Paper›PMID 28129640›Full record

ArticleOncotarget2017

Nuclear transport of cancer extracellular vesicle-derived biomaterials through nuclear envelope invagination-associated late endosomes.

Germana Rappa, Mark F Santos, Toni M Green, Jana Karbanová, Justin Hassler, Yongsheng Bai, Sanford H Barsky, Denis Corbeil, Aurelio Lorico

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 60 papers.

0numbers the graph read from it
0cells of the map it votes in
60citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

60 citing papers in PubMed, 77 citations in OpenAlex.

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  14. Mechanisms for assembly of the nucleoplasmic reticulum.Cellular and molecular life sciences : CMLS · 2024
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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

9 authors at 4 institutions in 2 countries.

Germana RappaRoseman Cancer Center and Department of Pathology, Roseman University College of Medicine, Las Vegas, NV, USA.
Mark F SantosRoseman Cancer Center and Department of Pathology, Roseman University College of Medicine, Las Vegas, NV, USA.
Toni M GreenRoseman Cancer Center and Department of Pathology, Roseman University College of Medicine, Las Vegas, NV, USA.
Jana KarbanováBiotechnology Center and DFG Research Center, Technische Universität Dresden, Tatzberg, Dresden, Germany.
Justin HasslerRoseman Cancer Center and Department of Pathology, Roseman University College of Medicine, Las Vegas, NV, USA.
Yongsheng BaiIndiana State University, Terre Haute, IN, USA.
Sanford H BarskyRoseman Cancer Center and Department of Pathology, Roseman University College of Medicine, Las Vegas, NV, USA.
Denis CorbeilBiotechnology Center and DFG Research Center, Technische Universität Dresden, Tatzberg, Dresden, Germany.
Aurelio LoricoRoseman Cancer Center and Department of Pathology, Roseman University College of Medicine, Las Vegas, NV, USA.
Roseman University of Health Sciences · USTU Dresden · DEHealth First · USIndiana State University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Extracellular membrane vesicles (EVs) function as vehicles of intercellular communication, but how the biomaterials they carry reach the target site in recipient cells is an open question. We report that subdomains of Rab7+ late endosomes and nuclear envelope invaginations come together to create a sub-nuclear compartment, where biomaterials associated with CD9+ EVs are delivered. EV-derived biomaterials were also found in the nuclei of host cells. The inhibition of nuclear import and export pathways abrogated the nuclear localization of EV-derived biomaterials or led to their accumulation therein, respectively, suggesting that their translocation is dependent on nuclear pores. Nuclear envelope invagination-associated late endosomes were observed in ex vivo biopsies in both breast carcinoma and associated stromal cells. The transcriptome of stromal cells exposed to cancer cell-derived CD9+ EVs revealed that the regulation of eleven genes, notably those involved in inflammation, relies on the nuclear translocation of EV-derived biomaterials. Our findings uncover a new cellular pathway used by EVs to reach nuclear compartment.

Indexed as

Active Transport, Cell NucleusAdultBiocompatible MaterialsBreast NeoplasmsCell CommunicationCells, CulturedEndosomesExosomesExtracellular VesiclesFemaleHumansInflammation MediatorsMesenchymal Stem CellsNuclear EnvelopeBiocompatible MaterialsInflammation Mediatorscancerendosomeextracellular vesiclemesenchymal stromal cellnuclear envelope invaginationtranscriptome

Identifiers

PMID28129640
PMCPMC5362417
OpenAlexW2581374376

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.