Evidence map›Paper›PMID 29124875›Full record

ReviewMolecular oncology2018

Emerging functions of the EGFR in cancer.

Sara Sigismund, Daniele Avanzato, Letizia Lanzetti

Open access · goldAbstract readReview
In one paragraph

Review in Molecular oncology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 812 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
812citing papers in PubMed, 2 pooled it
50.5field-weighted citation impact, top 1% 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

812 citing papers in PubMed, 2 syntheses or guidelines pooled it, 1,418 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Targeting Cancer Hallmarks withInternational journal of molecular sciences · 2026
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Internalization-Dependent EGFR-Targeted Photoactivation by Cetuximab-I21 Conjugates.Journal of immunotherapy (Hagerstown, Md. : 1997) · 2026
    Article
  17. Article
  18. Article
  19. Review
  20. Article

752 more citing papers are in PubMed but not listed here.

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 2 countries.

Sara SigismundFondazione Istituto FIRC di Oncologia Molecolare (IFOM), Milan, Italy.
Daniele AvanzatoDepartment of Oncology, University of Torino Medical School, Italy.
Letizia LanzettiDepartment of Oncology, University of Torino Medical School, Italy.ORCID 0000-0001-7541-5524
Department of Medical Sciences · BYIFOM · IT

Funding

Worldwide Cancer Research 16-1245
6 · The paper itself

Abstract

The physiological function of the epidermal growth factor receptor (EGFR) is to regulate epithelial tissue development and homeostasis. In pathological settings, mostly in lung and breast cancer and in glioblastoma, the EGFR is a driver of tumorigenesis. Inappropriate activation of the EGFR in cancer mainly results from amplification and point mutations at the genomic locus, but transcriptional upregulation or ligand overproduction due to autocrine/paracrine mechanisms has also been described. Moreover, the EGFR is increasingly recognized as a biomarker of resistance in tumors, as its amplification or secondary mutations have been found to arise under drug pressure. This evidence, in addition to the prominent function that this receptor plays in normal epithelia, has prompted intense investigations into the role of the EGFR both at physiological and at pathological level. Despite the large body of knowledge obtained over the last two decades, previously unrecognized (herein defined as 'noncanonical') functions of the EGFR are currently emerging. Here, we will initially review the canonical ligand-induced EGFR signaling pathway, with particular emphasis to its regulation by endocytosis and subversion in human tumors. We will then focus on the most recent advances in uncovering noncanonical EGFR functions in stress-induced trafficking, autophagy, and energy metabolism, with a perspective on future therapeutic applications.

Indexed as

AnimalsAutophagyCell MembraneEndocytosisEndosomesErbB ReceptorsHumansLigandsMiceMice, KnockoutNeoplasmsStress, PhysiologicalEGFR protein, humanErbB ReceptorsLigandscancerEGFRmembrane traffickingsignal transduction

Identifiers

PMID29124875
PMCPMC5748484
OpenAlexW2767336741

What OpenQuestion holds

Textmetadata
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.