Evidence map›Paper›PMID 10225980›Full record

ArticleThe Journal of clinical investigation1999

The trefoil gene family are coordinately expressed immediate-early genes: EGF receptor- and MAP kinase-dependent interregulation.

D Taupin, D C Wu, W K Jeon, K Devaney, T C Wang, D K Podolsky

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
11.8field-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

54 citing papers in PubMed, 153 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Investigation of the Relationship Between Trefoil Factor Family Peptides and Sinonasal Inflammation.Indian journal of otolaryngology and head and neck surgery : official publication of the Association of Otolaryngologists of India · 2023
    Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Article
  12. Article
  13. Differential Expression ofInternational journal of molecular sciences · 2019
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

6 authors at 4 institutions in 3 countries.

D TaupinGastrointestinal Unit and Center for the Study of Inflammatory Bowel Disease, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts 02114, USA.
D C Wu
W K Jeon
K Devaney
T C Wang
D K Podolsky
Harvard University Press · USHarvard University · USKaohsiung Medical University · TWSamsung (South Korea) · KR

Funding

Pilot & Feasibility ProgramP30DK043351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI RAYMOND T CHUNG · 1991 to 2026
$35.3M
PEPTIDE GROWTH FACTORS IN INTESTINAL EPITHELIAL REPAIRR37DK041557 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI PODOLSKY, DANIEL K · 1997 to 2006
$2.9M
PEPTIDE GROWTH FACTORS IN INTESTINAL EPITHELIAL REPAIRR01DK041557 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI PODOLSKY, DANIEL K · 1988 to 1997
–
NIDDK NIH HHS DK-41557NIDDK NIH HHS DK-43351NIDDK NIH HHS P30 DK043351NIDDK NIH HHS R01 DK041557NIDDK NIH HHS R37 DK041557
6 · The paper itself

Abstract

The trefoil gene family of mucus cell-secreted proteins is a critical mediator of gastrointestinal mucosal restitution. Transcription of trefoil genes is induced during mucosal repair, but the regulatory mechanisms involved are unknown. Mice deficient in the intestine-specific peptide intestinal trefoil factor (ITF), in which colonic restitution is lethally impaired, showed reduced expression of the gastric trefoil genes SP and pS2, suggesting that trefoil peptides may individually regulate transcription of the entire family. In gastric cell lines, the trefoils were shown to act in a manner suggestive of immediate-early genes capable of auto- and cross-induction through cis-acting regulatory regions. Trefoil-mediated transcriptional regulation required activation of the Ras/MEK/MAP kinase signal transduction pathway. EGF receptor (EGF-R) activation was also necessary for trefoil auto- and cross-induction, and both spasmolytic polypeptide (SP) and ITF stimulation of gastric cell lines led to phosphorylation of EGF-R. Nevertheless, ITF and ITF-thioredoxin cell surface binding at 4 degrees C colocalized not with EGF-R, but with CD71, which is found in clathrin-coated pits, suggesting that integration of trefoil peptide responses may occur after internalization. As EGF-R expression is itself strongly induced after mucosal damage, the trefoil/EGF-R relationship may be pivotal in the generation and maintenance of the mucosal repair phenotype.

Indexed as

Genes, Immediate-EarlyMucinsMuscle ProteinsNeuropeptidesAnimalsBase SequenceCalcium-Calmodulin-Dependent Protein KinasesClathrinDNA PrimersErbB ReceptorsGene Expression RegulationGrowth SubstancesHumansMicePeptidesPhosphorylationCalcium-Calmodulin-Dependent Protein KinasesClathrinDNA PrimersErbB ReceptorsGrowth SubstancesMucinsMuscle ProteinsNeuropeptidesPeptidesras ProteinsTff2 protein, ratTFF3 protein, ratTrefoil Factor-2Trefoil Factor-3

Identifiers

PMID10225980
PMCPMC408349
OpenAlexW1978596592

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.