Evidence map›Paper›PMID 28062852›Full record

ArticleJournal of cell science2017

A proteomic approach to identify endosomal cargoes controlling cancer invasiveness.

Jesica Diaz-Vera, Sarah Palmer, Juan Ramon Hernandez-Fernaud, Emmanuel Dornier, Louise E Mitchell, Iain Macpherson, Joanne Edwards, Sara Zanivan, Jim C Norman

Open access · hybridAbstract read
In one paragraph

Article in Journal of cell science, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.3field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
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  4. Neuropilin (NRPs) Related Pathological Conditions and Their Modulators.International journal of molecular sciences · 2022
    Review
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  10. Anthrax toxin requires ZDHHC5-mediated palmitoylation of its surface-processing host enzymes.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  11. 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

9 authors at 2 institutions in 1 country.

Jesica Diaz-VeraBeatson Institute for Cancer Research, Garscube Estate, Glasgow G61 1BD, UK.
Sarah PalmerBeatson Institute for Cancer Research, Garscube Estate, Glasgow G61 1BD, UK.
Juan Ramon Hernandez-FernaudBeatson Institute for Cancer Research, Garscube Estate, Glasgow G61 1BD, UK.
Emmanuel DornierBeatson Institute for Cancer Research, Garscube Estate, Glasgow G61 1BD, UK.
Louise E MitchellBeatson Institute for Cancer Research, Garscube Estate, Glasgow G61 1BD, UK.
Iain MacphersonBeatson Institute for Cancer Research, Garscube Estate, Glasgow G61 1BD, UK.
Joanne EdwardsWolfson Wohl Cancer Research Centre, Institute of Cancer Sciences, University of Glasgow, Glasgow G61 1QH, UK.
Sara ZanivanBeatson Institute for Cancer Research, Garscube Estate, Glasgow G61 1BD, UK s.zanivan@beatson.gla.ac.uk j.norman@beatson.gla.ac.uk.
Jim C NormanBeatson Institute for Cancer Research, Garscube Estate, Glasgow G61 1BD, UK s.zanivan@beatson.gla.ac.uk j.norman@beatson.gla.ac.uk.ORCID 0000-0002-0098-3014
Cancer Research UK Scotland Institute · GBUniversity of Glasgow · GB

Funding

Cancer Research UK 12935Cancer Research UK 18277Cancer Research UK C596/A12935Cancer Research UK C596/A17196Cancer Research UK C596/A18277Medical Research Council MR/P01058X/1
6 · The paper itself

Abstract

We have previously shown that Rab17, a small GTPase associated with epithelial polarity, is specifically suppressed by ERK2 (also known as MAPK1) signalling to promote an invasive phenotype. However, the mechanisms through which Rab17 loss permits invasiveness, and the endosomal cargoes that are responsible for mediating this, are unknown. Using quantitative mass spectrometry-based proteomics, we have found that knockdown of Rab17 leads to a highly selective reduction in the cellular levels of a v-SNARE (Vamp8). Moreover, proteomics and immunofluorescence indicate that Vamp8 is associated with Rab17 at late endosomes. Reduced levels of Vamp8 promote transition between ductal carcinoma

Indexed as

Amino AcidsBreast NeoplasmsCell Line, TumorEndosomesFemaleGene Knockdown TechniquesHumansIntracellular MembranesIsotope LabelingModels, BiologicalNeoplasm GradingNeoplasm InvasivenessNeuropilin-2Protein BindingProtein TransportProteomicsAmino AcidsNeuropilin-2neuropilin-2, humanrab GTP-Binding ProteinsReceptors, EstrogenRNA, MessengerR-SNARE ProteinsSNARE ProteinsVAMP8 protein, humanBreast cancerCell migrationDuctal carcinoma in situInvasionInvasive ductal carcinomaLate endosomeNeuropilin-2Rab17SILACVamp8

Identifiers

PMID28062852
PMCPMC5339883
OpenAlexW2567920517

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.