Evidence map›Paper›PMID 24966585›Full record

ReviewWorld journal of gastroenterology2014

Emerging role of the β-catenin-PPARγ axis in the pathogenesis of colorectal cancer.

Lina Sabatino, Massimo Pancione, Carolina Votino, Tommaso Colangelo, Angelo Lupo, Ettore Novellino, Antonio Lavecchia, Vittorio Colantuoni

Open access · hybridAbstract readReview
In one paragraph

Review in World journal of gastroenterology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
3.0field-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

36 citing papers in PubMed, 55 citations in OpenAlex.

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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

8 authors at 1 institution in 1 country.

Lina SabatinoLina Sabatino, Massimo Pancione, Carolina Votino, Tommaso Colangelo, Angelo Lupo, Vittorio Colantuoni, Department of Sciences and Technologies, University of Sannio, 82100 Benevento, Italy.
Massimo PancioneLina Sabatino, Massimo Pancione, Carolina Votino, Tommaso Colangelo, Angelo Lupo, Vittorio Colantuoni, Department of Sciences and Technologies, University of Sannio, 82100 Benevento, Italy.
Carolina VotinoLina Sabatino, Massimo Pancione, Carolina Votino, Tommaso Colangelo, Angelo Lupo, Vittorio Colantuoni, Department of Sciences and Technologies, University of Sannio, 82100 Benevento, Italy.
Tommaso ColangeloLina Sabatino, Massimo Pancione, Carolina Votino, Tommaso Colangelo, Angelo Lupo, Vittorio Colantuoni, Department of Sciences and Technologies, University of Sannio, 82100 Benevento, Italy.
Angelo LupoLina Sabatino, Massimo Pancione, Carolina Votino, Tommaso Colangelo, Angelo Lupo, Vittorio Colantuoni, Department of Sciences and Technologies, University of Sannio, 82100 Benevento, Italy.
Ettore NovellinoLina Sabatino, Massimo Pancione, Carolina Votino, Tommaso Colangelo, Angelo Lupo, Vittorio Colantuoni, Department of Sciences and Technologies, University of Sannio, 82100 Benevento, Italy.
Antonio LavecchiaLina Sabatino, Massimo Pancione, Carolina Votino, Tommaso Colangelo, Angelo Lupo, Vittorio Colantuoni, Department of Sciences and Technologies, University of Sannio, 82100 Benevento, Italy.
Vittorio ColantuoniLina Sabatino, Massimo Pancione, Carolina Votino, Tommaso Colangelo, Angelo Lupo, Vittorio Colantuoni, Department of Sciences and Technologies, University of Sannio, 82100 Benevento, Italy.
University of Sannio · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Multiple lines of evidence indicate that Wnt/β-catenin signaling plays a fundamental role in colorectal cancer (CRC) initiation and progression. Recent genome-wide data have confirmed that in CRC this pathway is one of the most frequently modified by genetic or epigenetic alterations affecting almost 90% of Wnt/β-catenin gene members. A major challenge is thus learning how the corrupted coordination of this pathway is tied to other signalings to enhance cell growth. Peroxisome proliferator activated receptor γ (PPARγ) is emerging as a growth-limiting and differentiation-promoting factor. In tumorigenesis it exerts a tumor suppressor role and is potentially linked with the Wnt/β-catenin pathway. Based on these results, the identification of new selective PPARγ modulators with inhibitory effects on the Wnt/β-catenin pathway is becoming an interesting perspective. Should, in fact, these molecules display such properties, new research avenues would be opened aimed at developing new molecular targeted drugs. Herein, we review the basic principles and present new hypotheses underlying the crosstalk between Wnt/β-catenin and PPARγ signaling. Furthermore, we discuss the advances in our understanding as to how their altered regulation can culminate in colon cancer and the efforts aimed at designing novel PPARγ agonists endowed with Wnt/β-catenin inhibitory effects to be used as therapeutic and/or preventive agents.

Indexed as

Wnt Signaling PathwayAnimalsAntineoplastic Agentsbeta CateninColorectal NeoplasmsDrug DesignHumansMolecular Targeted TherapyPPAR gammaAntineoplastic Agentsbeta CateninPPAR gammaColorectal cancerGenomic instabilityPeroxisome proliferator-activated receptor γPeroxisome proliferator activated receptor γ ligandsWnt/β-catenin pathway

Identifiers

PMID24966585
PMCPMC4064060
OpenAlexW2040817722

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.