Evidence map›Paper›PMID 31426451›Full record

ReviewCells2019

The NAE Pathway: Autobahn to the Nucleus for Cell Surface Receptors.

Poonam Shah, Alexandre Chaumet, Stephen J Royle, Frederic A Bard

Open access · goldAbstract readReview
In one paragraph

Review in Cells, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

15 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Protein sorting from endosomes to the TGN.Frontiers in cell and developmental biology · 2023
    Review
  10. Article
  11. Nucleolin: a cell portal for viruses, bacteria, and toxins.Cellular and molecular life sciences : CMLS · 2022
    Review
  12. Article
  13. Article
  14. Article
  15. Review
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

4 authors at 3 institutions in 2 countries.

Poonam ShahInstitute of Molecular and Cell Biology, Singapore 138673, Singapore.
Alexandre ChaumetInstitute of Molecular and Cell Biology, Singapore 138673, Singapore.
Stephen J RoyleCentre for Mechanochemical Cell Biology, Warwick Medical School, Coventry CV4 7AL, UK.
Frederic A BardInstitute of Molecular and Cell Biology, Singapore 138673, Singapore. fbard@imcb.a-star.edu.sg.
University of Warwick · GBInstitute of Molecular and Cell Biology · SGNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Various growth factors and full-length cell surface receptors such as EGFR are translocated from the cell surface to the nucleoplasm, baffling cell biologists to the mechanisms and functions of this process. Elevated levels of nuclear EGFR correlate with poor prognosis in various cancers. In recent years, nuclear EGFR has been implicated in regulating gene transcription, cell proliferation and DNA damage repair. Different models have been proposed to explain how the receptors are transported into the nucleus. However, a clear consensus has yet to be reached. Recently, we described the nuclear envelope associated endosomes (NAE) pathway, which delivers EGFR from the cell surface to the nucleus. This pathway involves transport, docking and fusion of NAEs with the outer membrane of the nuclear envelope. EGFR is then presumed to be transported through the nuclear pore complex, extracted from membranes and solubilised. The SUN1/2 nuclear envelope proteins, Importin-beta, nuclear pore complex proteins and the Sec61 translocon have been implicated in the process. While this framework can explain the cell surface to nucleus traffic of EGFR and other cell surface receptors, it raises several questions that we consider in this review, together with implications for health and disease.

Indexed as

beta KaryopherinsCell LineEndocytosisEndosomesErbB ReceptorsHumansMembrane ProteinsMicrotubule-Associated ProteinsNuclear EnvelopeNuclear Pore Complex ProteinsNuclear ProteinsSEC Translocation Channelsbeta KaryopherinsEGFR protein, humanErbB ReceptorsMembrane ProteinsMicrotubule-Associated ProteinsNuclear Pore Complex ProteinsNuclear ProteinsSEC Translocation ChannelsSUN1 protein, humanEGFRinsulin receptornuclear associated endosomes (NAE)nuclear envelope, SUN, translocon

Identifiers

PMID31426451
PMCPMC6721735
OpenAlexW2968298560

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.