Evidence map›Paper›PMID 15084607›Full record

ArticleThe Journal of biological chemistry2004

Wnt11 signaling promotes proliferation, transformation, and migration of IEC6 intestinal epithelial cells.

Lillian Ouko, Thomas R Ziegler, Li H Gu, Leonard M Eisenberg, Vincent W Yang

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 61 papers.

0numbers the graph read from it
0cells of the map it votes in
61citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

61 citing papers in PubMed, 109 citations in OpenAlex.

  1. Trial
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  3. Wnt/CaOncology letters · 2025
    Review
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1 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 at 3 institutions in 1 country.

Lillian OukoDivisions of Digestive Diseases and Endocrinology, Department of Medicine, Winship Cancer Institute, Emory University School of Medicine, Atlanta, Georgia 30322, USA.
Thomas R Ziegler
Li H Gu
Leonard M Eisenberg
Vincent W Yang
Emory University · USMedical University of South Carolina · USWinship Cancer Institute

Funding

REGULATION OF INTESTINAL EPITHELIAL CELL PROLIFERATIONR01DK052230 · NIDDK · STATE UNIVERSITY NEW YORK STONY BROOK · PI Vincent W Yang · 1997 to 2026
$8.7M
MECHANISMS OF INTESTINAL TUMORIGENESISR01CA084197 · NCI · STATE UNIVERSITY NEW YORK STONY BROOK · PI YANG, VINCENT W · 2000 to 2020
$7.5M
Emory Epithelial Pathobiology Research Development CenterR24DK064399 · NIDDK · EMORY UNIVERSITY · PI PARKOS, CHARLES A · 2003 to 2012
$5.3M
DIET/GROWTH FACTOR MECHANISMS OF GUT ADAPTATIONR01DK055850 · NIDDK · EMORY UNIVERSITY · PI ZIEGLER, THOMAS R · 2000 to 2004
$1.5M
NCI NIH HHS CA84197NCI NIH HHS R01 CA084197NIDDK NIH HHS DK52230NIDDK NIH HHS DK55850NIDDK NIH HHS DK64399NIDDK NIH HHS R01 DK052230NIDDK NIH HHS R01 DK055850NIDDK NIH HHS R24 DK064399
6 · The paper itself

Abstract

Wnts are morphogens with well recognized functions during embryogenesis. Aberrant Wnt signaling has been demonstrated to be important in colorectal carcinogenesis. However, the role of Wnt in regulating normal intestinal epithelial cell proliferation is not well established. Here we determine that Wnt11 is expressed throughout the mouse intestinal tract including the epithelial cells. Conditioned media from Wnt11-secreting cells stimulated proliferation and migration of IEC6 intestinal epithelial cells. Co-culture of Wnt11-secreting cells with IEC6 cells resulted in morphological transformation of the latter as evidenced by the formation of foci, a condition also accomplished by stable transfection of IEC6 with a Wnt11-expressing construct. Treatment of IEC6 cells with Wnt11 conditioned media failed to induce nuclear translocation of beta-catenin but led to increased activities of protein kinase C and Ca(2+)/calmodulin-dependent protein kinase II. Inhibition of protein kinase C resulted in a decreased ability of Wnt11 to induce foci formation in IEC6 cells. Finally, E-cadherin was redistributed in Wnt11-treated IEC6 cells, resulting in diminished E-cadherin-mediated cell-cell contact. We conclude that Wnt11 stimulates proliferation, migration, cytoskeletal rearrangement, and contact-independent growth of IEC6 cells by a beta-catenin-independent mechanism. These findings may help understand the molecular mechanisms that regulate proliferation and migration of intestinal epithelial cells.

Indexed as

Active Transport, Cell NucleusAnimalsbeta CateninBlotting, NorthernBlotting, WesternCaco-2 CellsCell DifferentiationCell DivisionCell LineCell Line, TumorCell MovementCell Transformation, NeoplasticCoculture TechniquesCulture Media, ConditionedCytoskeletal ProteinsCytoskeletonbeta CateninCTNNB1 protein, humanCtnnb1 protein, ratCulture Media, ConditionedCytoskeletal ProteinsGlycoproteinsLuciferasesProtein Kinase CTrans-ActivatorsWnt Proteins

Identifiers

PMID15084607
PMCPMC1351009
OpenAlexW2112015741

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.