Evidence map›Paper›PMID 9508783›Full record

ArticleThe Journal of cell biology1998

KSA antigen Ep-CAM mediates cell-cell adhesion of pancreatic epithelial cells: morphoregulatory roles in pancreatic islet development.

V Cirulli, L Crisa, G M Beattie, M I Mally, A D Lopez, A Fannon, A Ptasznik, L Inverardi, C Ricordi, T Deerinck and 3 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of cell biology, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
8.8field-weighted citation impact, top 2% 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

46 citing papers in PubMed, 106 citations in OpenAlex.

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  13. Review
  14. Shedding light on the EpCAM: An overview.Journal of cellular physiology · 2019
    Review
  15. Review
  16. Article
  17. Functions of EpCAM in physiological processes and diseases (Review).International journal of molecular medicine · 2018
    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

13 authors at 4 institutions in 1 country.

V CirulliThe Islet Research Laboratory at The Whittier Institute for Diabetes, Department of Pediatrics, University of California at San Diego, La Jolla, CA 92037, USA. vincenzo@alex.ucsd.edu
L Crisa
G M Beattie
M I Mally
A D Lopez
A Fannon
A Ptasznik
L Inverardi
C Ricordi
T Deerinck
M Ellisman
R A Reisfeld
A Hayek
Scripps Research Institute · USUniversity of Miami · USIcahn School of Medicine at Mount Sinai · USUniversity of California, San Diego · US

Funding

VOLUMETRIC CONTOUR-BASED SURFACE RECONSTRUCTIONP41RR004050 · NCRR · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI PASQUALE, ELENA B · 1989 to 2011
$28.0M
ISLET TRANSPLANTATION IN EXPERIMENTAL DIABETESR01DK039087 · NIDDK · WHITTIER INSTITUTE FOR DIABETES &ENDOC · PI HAYEK, ALBERTO · 1989 to 1995
–
NCRR NIH HHS P41 RR004050NCRR NIH HHS RR-04050NIDDK NIH HHS DK-39087
6 · The paper itself

Abstract

Cell adhesion molecules (CAMs) are important mediators of cell-cell interactions and regulate cell fate determination by influencing growth, differentiation, and organization within tissues. The human pancarcinoma antigen KSA is a glycoprotein of 40 kD originally identified as a marker of rapidly proliferating tumors of epithelial origin. Interestingly, most normal epithelia also express this antigen, although at lower levels, suggesting that a dynamic regulation of KSA may occur during cell growth and differentiation. Recently, evidence has been provided that this glycoprotein may function as an epithelial cell adhesion molecule (Ep-CAM). Here, we report that Ep-CAM exhibits the features of a morphoregulatory molecule involved in the development of human pancreatic islets. We demonstrate that Ep-CAM expression is targeted to the lateral domain of epithelial cells of the human fetal pancreas, and that it mediates calcium-independent cell-cell adhesion. Quantitative confocal immunofluorescence in fetal pancreata identified the highest levels of Ep-CAM expression in developing islet-like cell clusters budding from the ductal epithelium, a cell compartment thought to comprise endocrine progenitors. A surprisingly reversed pattern was observed in the human adult pancreas, displaying low levels of Ep-CAM in islet cells and high levels in ducts. We further demonstrate that culture conditions promoting epithelial cell growth induce upregulation of Ep-CAM, whereas endocrine differentiation of fetal pancreatic epithelial cells, transplanted in nude mice, is associated with a downregulation of Ep-CAM expression. In addition, a blockade of Ep-CAM function by KS1/4 mAb induced insulin and glucagon gene transcription and translation in fetal pancreatic cell clusters. These results indicate that developmentally regulated expression and function of Ep-CAM play a morphoregulatory role in pancreatic islet ontogeny.

Indexed as

AdultAge FactorsAnimalsAntigens, NeoplasmBiomarkers, TumorCell AdhesionCell Adhesion MoleculesCell DifferentiationCell DivisionEpithelial Cell Adhesion MoleculeEpithelial CellsFemaleFetusHumansIslets of LangerhansMembrane GlycoproteinsAntigens, NeoplasmBiomarkers, TumorCell Adhesion MoleculesEpithelial Cell Adhesion MoleculeMembrane Glycoproteins

Identifiers

PMID9508783
PMCPMC2132663
OpenAlexW2116153053

What OpenQuestion 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 OpenQuestion graph.