Evidence map›Paper›PMID 28281543›Full record

ArticleNature communications2017

EGFR/ARF6 regulation of Hh signalling stimulates oncogenic Ras tumour overgrowth.

Chiswili Chabu, Da-Ming Li, Tian Xu

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.7field-weighted citation impact, top 16% 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

16 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  9. Review
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  12. Prp8 regulates oncogene-induced hyperplastic growth inDevelopment (Cambridge, England) · 2018
    Article
  13. Review
  14. Article
  15. Article
  16. Modelling Cooperative Tumorigenesis inBioMed research international · 2018
    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

3 authors at 2 institutions in 1 country.

Chiswili ChabuDepartment of Genetics, Howard Hughes Medical Institute, Yale University School of Medicine, Boyer Center for Molecular Medicine, 295 Congress Avenue, New Haven, Connecticut 06536, USA.
Da-Ming LiDepartment of Genetics, Howard Hughes Medical Institute, Yale University School of Medicine, Boyer Center for Molecular Medicine, 295 Congress Avenue, New Haven, Connecticut 06536, USA.
Tian XuDepartment of Genetics, Howard Hughes Medical Institute, Yale University School of Medicine, Boyer Center for Molecular Medicine, 295 Congress Avenue, New Haven, Connecticut 06536, USA.
Yale University · USHoward Hughes Medical Institute · US

Funding

TUMOR SUPPRESSORS AND CELL PROLIFERATION IN DROSOPHILAR01CA069408 · NCI · YALE UNIVERSITY · PI XU, TIAN · 1996 to 2016
$5.1M
Live analysis of tumor-host cells interactionsF32CA142118 · NCI · YALE UNIVERSITY · PI CHABU, CHISWILI YVES · 2010 to 2012
$104k
NCI NIH HHS F32 CA142118NCI NIH HHS R01 CA069408
6 · The paper itself

Abstract

Multiple signalling events interact in cancer cells. Oncogenic Ras cooperates with Egfr, which cannot be explained by the canonical signalling paradigm. In turn, Egfr cooperates with Hedgehog signalling. How oncogenic Ras elicits and integrates Egfr and Hedgehog signals to drive overgrowth remains unclear. Using a Drosophila tumour model, we show that Egfr cooperates with oncogenic Ras via Arf6, which functions as a novel regulator of Hh signalling. Oncogenic Ras induces the expression of Egfr ligands. Egfr then signals through Arf6, which regulates Hh transport to promote Hh signalling. Blocking any step of this signalling cascade inhibits Hh signalling and correspondingly suppresses the growth of both, fly and human cancer cells harbouring oncogenic Ras mutations. These findings highlight a non-canonical Egfr signalling mechanism, centered on Arf6 as a novel regulator of Hh signalling. This explains both, the puzzling requirement of Egfr in oncogenic Ras-mediated overgrowth and the cooperation between Egfr and Hedgehog.

Indexed as

Gene Expression Regulation, NeoplasticADP-Ribosylation Factor 6ADP-Ribosylation FactorsAnimalsCell Line, TumorDisease Models, AnimalDrosophila melanogasterDrosophila ProteinsEpithelial CellsErbB ReceptorsGenes, ReporterGreen Fluorescent ProteinsHedgehog ProteinsHumansImaginal DiscsIMP DehydrogenaseADP-Ribosylation Factor 6ADP-Ribosylation FactorsARF6 protein, humanDrosophila ProteinsEgfr protein, DrosophilaErbB ReceptorsGreen Fluorescent ProteinsHedgehog Proteinshh protein, DrosophilaIMP Dehydrogenaseras protein, DrosophilaReceptors, Invertebrate Peptide

Identifiers

PMID28281543
PMCPMC5353614
OpenAlexW2594353026

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.