Evidence map›Paper›PMID 24430869›Full record

ArticleMolecular biology of the cell2014

The ShcD signaling adaptor facilitates ligand-independent phosphorylation of the EGF receptor.

Melanie K B Wills, Jiefei Tong, Sylvie L Tremblay, Michael F Moran, Nina Jones

Abstract read
In one paragraph

Article in Molecular biology of the cell, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 21% 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, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Adaptor Protein ShcD/Molecular cancer research : MCR · 2021
    Article
  8. Receptor Tyrosine Kinase Signaling and Targeting in Glioblastoma Multiforme.International journal of molecular sciences · 2021
    Review
  9. Article
  10. Article
  11. Affinity purification mass spectrometry analysis of PD-1 uncovers SAP as a new checkpoint inhibitor.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  12. Article
  13. Article
  14. Article
  15. Article
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

5 authors at 3 institutions in 1 country.

Melanie K B WillsDepartment of Molecular and Cellular Biology, University of Guelph, Guelph, ON N1G 2W1, Canada Program in Molecular Structure and Function, Hospital for Sick Children, Toronto, ON M5G 1X8, Canada Department of Molecular Genetics and Banting and Best Department of Medical Research, University of Toronto, Toronto, ON M5G 1L6, Canada.
Jiefei Tong
Sylvie L Tremblay
Michael F Moran
Nina Jones
University of Guelph · CAHospital for Sick Children · CAUniversity of Toronto · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Proto-oncogenic Src homology and collagen (Shc) proteins have been considered archetypal adaptors of epidermal growth factor receptor (EGFR)-mediated signaling. We report that in addition to its role as an EGFR-binding partner and Grb2 platform, ShcD acts noncanonically to promote phosphorylation of select EGFR residues. Unexpectedly, Y1068, Y1148, and Y1173 are subject to ShcD-induced, cell-autonomous hyperphosphorylation in the absence of external stimuli. This response is not elicited by other Shc proteins and requires the intrinsic EGFR kinase, as well as the ShcD phosphotyrosine-binding (PTB) domain. Assessments of Erk, Akt, phospholipase C 1γ, and FAK pathways reveal no apparent distal signaling targets of ShcD. Nevertheless, the capacity of cultured cells to repopulate a wounded monolayer is markedly accelerated by ShcD in an EGFR kinase-dependent manner. Furthermore, detection of overexpressed ShcD coincident with EGFR phosphorylation in human gliomas suggests a clinical application for these findings. We thus demonstrate unique and relevant synergy between ShcD and EGFR that is unprecedented among signaling adaptors.

Indexed as

Amino Acid SequenceAnimalsBinding SitesBrain NeoplasmsChlorocebus aethiopsCOS CellsErbB ReceptorsExtracellular Signal-Regulated MAP KinasesFocal Adhesion Kinase 1Gene Expression RegulationGliomaHumansLigandsMolecular Sequence DataPhospholipase C gammaPhosphorylationErbB ReceptorsExtracellular Signal-Regulated MAP KinasesFocal Adhesion Kinase 1LigandsPhospholipase C gammaProto-Oncogene Proteins c-aktPTK2 protein, humanSHC4 protein, humanShc Signaling Adaptor Proteins

Identifiers

PMID24430869
PMCPMC3952845
OpenAlexW2165850683

What Socratic holds

Textmetadata
LicenceCC BY-NC-SA
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 Socratic graph.