Evidence map›Paper›PMID 22094462›Full record

ArticleThe Journal of biological chemistry2012

Negative cross-talk between calcium-sensing receptor and β-catenin signaling systems in colonic epithelium.

Osvaldo Rey, Wenhan Chang, Daniel Bikle, Nora Rozengurt, Steven H Young, Enrique Rozengurt

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing papers in PubMed
3.1field-weighted citation impact, top 8% 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

32 citing papers in PubMed, 65 citations in OpenAlex.

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  10. Intestinal GPCRs Control Paneth Cell Maturation and Susceptibility to Experimental Colitis.Cellular and molecular gastroenterology and hepatology · 2016
    Article
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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 1 country.

Osvaldo ReyUnit of Signal Transduction and Gastrointestinal Cancer, Division of Digestive Diseases, Department of Medicine, CURE: Digestive Diseases Research Center, David Geffen School of Medicine, UCLA, Los Angeles, California 90095, USA. orey@mednet.ucla.edu
Wenhan Chang
Daniel Bikle
Nora Rozengurt
Steven H Young
Enrique Rozengurt
UCLA Jonsson Comprehensive Cancer CenterVeterans Health Administration · USCenter for Digestive and Liver Diseases · USUniversity of California, Los Angeles · US

Funding

Pilot and Feasibility ProgramP30DK041301 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1990 to 2019
$18.0M
GASTROINTESTINAL PEPTIDE SIGNALING THROUGH PKC/PKDR01DK055003 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 1999 to 2011
$4.9M
Role of IGF-I/integrin signaling in the periosteal response to loadR01AR055924 · NIAMS · NORTHERN CALIFORNIA INSTITUTE/RES/EDU · PI BIKLE, DANIEL DAVID · 2008 to 2019
$3.5M
Vitamin D Receptor Coactivators in KeratinocytesR01AR050023 · NIAMS · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI BIKLE, DANIEL DAVID · 2004 to 2014
$3.4M
IGF-1 MEDIATES THE ANABOLIC EFFECTS OF PTH ON BONER01DK054793 · NIDDK · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI BIKLE, DANIEL DAVID · 2001 to 2012
$3.1M
GI PEPTIDE SIGNALING THROUGH TYROSINE PHOSPHORYLATIONR01DK056930 · NIDDK · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI ROZENGURT, JUAN ENRIQUE · 2000 to 2010
$3.0M
CALCIUM-SENSING RECEPTORS AND GROWTH PLATE DEVELOPMENTR01AG021353 · NIA · UNIVERSITY OF CALIFORNIA SAN FRANCISCO · PI CHANG, WENHAN · 2002 to 2012
$2.5M
Calcium Sensing Receptor Signaling in the Gastrointestinal TractK22CA128883 · NCI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI REY, OSVALDO A · 2007 to 2009
$528k
NCI NIH HHS K22 CA128883NCI NIH HHS K22CA128883NCI NIH HHS K22CA128883-03S1NIAMS NIH HHS R01 AR050023NIAMS NIH HHS R01AR050023NIAMS NIH HHS R01 AR055924NIA NIH HHS R01 AG021353NIA NIH HHS R01-AG21353NIDDK NIH HHS P30 DK041301NIDDK NIH HHS P30DK41301NIDDK NIH HHS R01 DK054793NIDDK NIH HHS R01DK054793NIDDK NIH HHS R01 DK055003NIDDK NIH HHS R01 DK056930NIDDK NIH HHS R01DK55003NIDDK NIH HHS R01DK56930
6 · The paper itself

Abstract

Here, we examined the role of the extracellular Ca(2+)-sensing receptor (CaSR) in the control of colonic epithelial cell proliferation in vivo and changes in β-catenin triggered by CaSR stimulation in human colonic epithelial cells in vitro. The in vivo studies, using a novel Casr intestinal-specific knock-out mouse, indicate that the genetic ablation of the Casr leads to hyperproliferation of colonic epithelial cells, expansion of the proliferative zone, changes in crypt structure, and enhanced β-catenin nuclear localization. The in vitro results indicate that stimulation of the CaSR, by Ca(2+) or by the calcimimetic R-568, produced a striking and time-dependent decrease in the phosphorylation of β-catenin at Ser-552 and Ser-675, two amino acid residues that promote β-catenin transcriptional activity. The reduced phosphorylation of β-catenin coincided with a decline in its nuclear localization and a marked redistribution to the plasma membrane. Furthermore, CaSR stimulation promoted a down-regulation of β-catenin-mediated transcriptional activation. These studies demonstrate that signaling pathways emanating from the CaSR control colonic epithelial cell proliferation in vivo and suggest that the mechanism involves regulation of β-catenin phosphorylation.

Indexed as

Active Transport, Cell NucleusAniline CompoundsAnimalsbeta CateninCalciumCalcium SignalingCell LineCell NucleusCell ProliferationColonDown-RegulationHumansIntestinal MucosaMiceMice, KnockoutPhenethylaminesAniline Compoundsbeta CateninCalciumCASR protein, humanN-(2-chlorophenylpropyl)-1-(3-methoxyphenyl)ethylaminePhenethylaminesPropylaminesReceptors, Calcium-Sensing

Identifiers

PMID22094462
PMCPMC3256874
OpenAlexW2028922188

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.