Evidence map›Paper›PMID 10449430›Full record

ArticleThe Journal of clinical investigation1999

A novel therapy for colitis utilizing PPAR-gamma ligands to inhibit the epithelial inflammatory response.

C G Su, X Wen, S T Bailey, W Jiang, S M Rangwala, S A Keilbaugh, A Flanigan, S Murthy, M A Lazar, G D Wu

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 217 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
217citing papers in PubMed, 1 pooled it
17.1field-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

217 citing papers in PubMed, 1 synthesis or guideline pooled it, 755 citations in OpenAlex.

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157 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

10 authors at 3 institutions in 1 country.

C G SuDivision of Gastroenterology, University of Pennsylvania School of Medicine, Philadelphia, Pennsylvania 19104, USA.
X Wen
S T Bailey
W Jiang
S M Rangwala
S A Keilbaugh
A Flanigan
S Murthy
M A Lazar
G D Wu
University Gastroenterology · USUniversity of Pennsylvania · USHahnemann University Hospital · US

Funding

TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 1997 to 2026
$32.5M
ZINC FINGER PROTEINS IN EARLY KIDNEY DEVELOPMENTP01DK049210 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI BIRNBAUM, MORRIS J · 1995 to 2016
$26.9M
Nuclear Receptors in Metabolic TissuesR01DK049780 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI LAZAR, MITCHELL A. · 1995 to 2025
$10.8M
IMMUNE MODULATION BY INTESTINAL CELL DIFFERENTIATIONR01AI039368 · NIAID · UNIVERSITY OF PENNSYLVANIA · PI WU, GARY D. · 1995 to 2009
$3.3M
INTESTINAL EPITHELIAL RESPONSE TO INFLAMMATIONR29DK047709 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI WU, GARY D. · 1993 to 1997
–
NIAID NIH HHS AI-39368NIAID NIH HHS R01 AI039368NIDDK NIH HHS DK-47709NIDDK NIH HHS P01 DK049210NIDDK NIH HHS P30 DK050306NIDDK NIH HHS P30 DK-50306NIDDK NIH HHS R01 DK049780
6 · The paper itself

Abstract

Peroxisome proliferator-activated receptor gamma (PPAR-gamma), a member of the nuclear hormone receptor superfamily originally shown to play a critical role in adipocyte differentiation and glucose homeostasis, has recently been implicated as a regulator of cellular proliferation and inflammatory responses. Colonic epithelial cells, which express high levels of PPAR-gamma protein, have the ability to produce inflammatory cytokines that may play a role in inflammatory bowel disease (IBD). We report here that PPAR-gamma ligands dramatically attenuate cytokine gene expression in colon cancer cell lines by inhibiting the activation of nuclear factor-kappaB via an IkappaB-alpha-dependent mechanism. Moreover, thiazolidinedione ligands for PPAR-gamma markedly reduce colonic inflammation in a mouse model of IBD. These results suggest that colonic PPAR-gamma may be a therapeutic target in humans suffering from IBD.

Indexed as

I-kappa B ProteinsThiazolidinedionesAnimalsCaco-2 CellsColitisCytokinesDNA-Binding ProteinsEpitheliumGene ExpressionHT29 CellsHumansInflammationInflammatory Bowel DiseasesInterleukin-8LigandsMice15-deoxy-delta(12,14)-prostaglandin J2CytokinesDNA-Binding ProteinsI-kappa B ProteinsInterleukin-8LigandsNF-kappa BNF-KappaB Inhibitor alphaNFKBIA protein, humanNfkbia protein, mouseProstaglandin D2Receptors, Cytoplasmic and NuclearRosiglitazoneThiazolesThiazolidinedionesTranscription Factors

Identifiers

PMID10449430
PMCPMC408529
OpenAlexW2003115027

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.