Evidence map›Paper›PMID 11106559›Full record

ArticleThe American journal of pathology2000

Modulation of human colon tumor-stromal interactions by the endothelin system.

G Egidy, L Juillerat-Jeanneret, J F Jeannin, P Korth, F T Bosman, F Pinet

Open access · greenAbstract read
In one paragraph

Article in The American journal of pathology, 2000. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.5field-weighted citation impact, top 12% 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

20 citing papers in PubMed, 78 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Article
  10. Endothelin-3 stimulates survival of goblet cells in organotypic cultures of fetal human colonic epithelium.American journal of physiology. Gastrointestinal and liver physiology · 2008
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Endothelin receptors as novel targets in tumor therapy.Journal of translational medicine · 2004
    Article
  17. Review
  18. Article
  19. Article
  20. 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

6 authors at 3 institutions in 2 countries.

G EgidyINSERM Unit 36, College of France, Paris, France. Lausanne, Switzerland. INSERM U517/Ecole Pratique des Hautes Etudes, Dijon, France.
L Juillerat-Jeanneret
J F Jeannin
P Korth
F T Bosman
F Pinet
Inserm · FRMetabolism and Renal Physiology · FRTaipei Institute of Pathology · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumor neovascularization is considered to be a critical step in the development of a malignant tumor. Endothelin (ET)-1 is a powerful vasoconstrictor and mitogenic peptide that is produced by many cancer cell lines. The cellular distribution of the ET components was evaluated in human colon tumors and compared to normal colon. There was more of the ET components (preproET-1, endothelin-converting enzyme-1, and ETA and ETB receptors) in adenomas and adenocarcinomas than in the normal colon. There was overproduction of preproET-1 and endothelin-converting enzyme-1 in carcinoma cells and stromal vessels, suggesting that they are a local source of ET-1. ETA receptors were present in stromal myofibroblasts of neoplastic tissue, and there were large amounts of ETB receptors in the endothelium and myofibroblasts. There was also a redistribution of alpha-smooth muscle actin-positive cells in the vascular structures of tumors. An experimental rat model of induced colon cancer treated for 30 days with bosentan, a mixed antagonist of both ET receptors, confirmed the morphological changes observed during the tumor vascularization. Our data suggest that ET-1 and its receptor play a role in colon cancer progression, with ET-1 functioning as a negative modulator of the stromal response.

Indexed as

AdenocarcinomaAdultAgedAged, 80 and overAnimalsAspartic Acid EndopeptidasesBosentanColonColonic NeoplasmsEndothelin-1Endothelin-Converting EnzymesEndothelin Receptor AntagonistsEndothelinsFemaleHumansMaleAspartic Acid EndopeptidasesBosentanECE1 protein, humanEndothelin-1Endothelin-Converting EnzymesEndothelin Receptor AntagonistsEndothelinsMetalloendopeptidasesProtein PrecursorsReceptor, Endothelin AReceptor, Endothelin BReceptors, EndothelinRNA, MessengerSulfonamides

Identifiers

PMID11106559
PMCPMC1885757
OpenAlexW2000132697

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.