Evidence map›Paper›PMID 19135477›Full record

ReviewPharmacology & therapeutics2009

Functional selectivity of EGF family peptide growth factors: implications for cancer.

Kristy J Wilson, Jennifer L Gilmore, John Foley, Mark A Lemmon, David J Riese

Abstract readReview
In one paragraph

Review in Pharmacology & therapeutics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 140 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
140citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

140 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Association between epidermal growth factor gene rs4444903 polymorphism and risk of glioma.Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine · 2013
    Pooled it
  2. Review
  3. Review
  4. Review
  5. Article
  6. Article
  7. Article
  8. The role of kinase domain dimerization in EGFR activation.Structure (London, England : 1993) · 2026
    Article
  9. Article
  10. Article
  11. Beyond the membrane: rethinking EGFR signaling in physiology and cancer.Cellular and molecular life sciences : CMLS · 2026
    Review
  12. Article
  13. Neuregulin 4 in Insulin Resistance: Mechanisms, Controversies, and Therapeutic Perspectives.Diabetes, metabolic syndrome and obesity : targets and therapy · 2026
    Review
  14. Review
  15. Article
  16. Amphiregulin in Fibrotic Diseases and Cancer.International journal of molecular sciences · 2025
    Review
  17. Article
  18. Structure and organization of full-length epidermal growth factor receptor in extracellular vesicles by cryo-electron tomography.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  19. Article
  20. Review

80 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

5 authors.

Kristy J WilsonPurdue University School of Pharmacy and Purdue Cancer Research Center, West Lafayette, IN 47907-2064, USA.
Jennifer L Gilmore
John Foley
Mark A Lemmon
David J Riese

Funding

ERBB RECEPTOR HOMO- AND HETERO- DIMERIZATIONR01CA079992 · NCI · UNIVERSITY OF PENNSYLVANIA · PI LEMMON, MARK A · 1999 to 2013
$3.7M
REGULATION OF EPIDERMAL DIFFERENTATION BY PTHRPR01AR045585 · NIAMS · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FOLEY, JOHN GREGORY · 2000 to 2004
$1.4M
Regulation of ErbB4 Signaling by Neuregulin IsoformsR01CA114209 · NCI · PURDUE UNIVERSITY · PI RIESE, DAVID J. · 2006 to 2010
$1.2M
ErbB1 signaling and cancer-mediated diseases of boneR21DK067875 · NIDDK · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI FOLEY, JOHN GREGORY · 2005 to 2006
$299k
TUMOR CELL LINE PROLIFERATION, MOTILITY AND INVASIVENESSR21CA080770 · NCI · PURDUE UNIVERSITY WEST LAFAYETTE · PI RIESE, DAVID J. · 1999 to 2000
$114k
NCI NIH HHS CA080770NCI NIH HHS CA114209NCI NIH HHS R01 CA079992NCI NIH HHS R01 CA114209NCI NIH HHS R21 CA080770NIAMS NIH HHS AR045585NIAMS NIH HHS R01 AR045585NIDDK NIH HHS DK067875NIDDK NIH HHS R21 DK067875
6 · The paper itself

Abstract

Breast, prostate, pancreatic, colorectal, lung, and head and neck cancers exploit deregulated signaling by ErbB family receptors and their ligands, EGF family peptide growth factors. EGF family members that bind the same receptor are able to stimulate divergent biological responses both in cell culture and in vivo. This is analogous to the functional selectivity exhibited by ligands for G-protein coupled receptors. Here we review this literature and propose that this functional selectivity of EGF family members is due to distinctions in the conformation of the liganded receptor and subsequent differences in the sites of receptor tyrosine phosphorylation and receptor coupling to signaling effectors. We also discuss the roles of divergent ligand activity in establishing and maintaining malignant phenotypes. Finally, we discuss the potential of mutant EGF family ligands as cancer chemotherapeutics targeted to ErbB receptors.

Indexed as

Amino Acid SequenceAnimalsAntineoplastic AgentsDrug Delivery SystemsEpidermal Growth FactorErbB ReceptorsHumansLigandsNeoplasmsSignal TransductionAntineoplastic AgentsEpidermal Growth FactorErbB ReceptorsLigands

Identifiers

PMID19135477
PMCPMC2665203

What OpenQuestion holds

Textmetadata
LicenceTDM
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.