Evidence map›Paper›PMID 27167203›Full record

ArticleOncotarget2016

Reduction in promotor methylation utilizing EGCG (epigallocatechin-3-gallate) restores RXRα expression in human colon cancer cells.

Jay Morris, Vondina R Moseley, April B Cabang, Katie Coleman, Wei Wei, Elizabeth Garrett-Mayer, Michael J Wargovich

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 pooled it
6.1field-weighted citation impact, top 3% 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

30 citing papers in PubMed, 1 synthesis or guideline pooled it, 59 citations in OpenAlex.

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  17. [Epigallocatechin gallate inducesNan fang yi ke da xue xue bao = Journal of Southern Medical University · 2020
    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

7 authors at 2 institutions in 1 country.

Jay MorrisDepartment of Molecular Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Vondina R MoseleyDepartment of Cell & Molecular Pharmacology, Medical University of South Carolina, Charleston, SC 29425, USA.
April B CabangDepartment of Molecular Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Katie ColemanDepartment of Cell & Molecular Pharmacology, Medical University of South Carolina, Charleston, SC 29425, USA.
Wei WeiDepartment of Public Health Science, Medical University of South Carolina, Charleston, SC 29425, USA.
Elizabeth Garrett-MayerDepartment of Biostatistics & Epidemiology, Medical University of South Carolina, Charleston, SC 29425, USA.
Michael J WargovichDepartment of Molecular Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX 78229, USA.
Medical University of South Carolina · USThe University of Texas Health Science Center at San Antonio · US

Funding

TISSUE CULTURE---COREP30CA054174 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Robin Jean Leach · 1991 to 2026
$59.1M
Tea Modulation of Colon CarcinogenesisR01CA096694 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI WARGOVICH, MICHAEL · 2002 to 2014
$2.6M
NCI NIH HHS P30 CA054174NCI NIH HHS R01 CA096694
6 · The paper itself

Abstract

Silencing of regulatory genes through hypermethylation of CpG islands is an important mechanism in tumorigenesis. In colon cancer, RXRα, an important dimerization partner with other nuclear transcription factors, is silenced through this mechanism. We previously found that colon tumors in ApcMin/+ mice had diminished levels of RXRα protein and expression levels of this gene were restored by treatment with a green tea intervention, due to reduced promoter methylation of RXRα. We hypothesized that CIMP+ cell lines, which epigenetically silence key regulatory genes would also evidence silencing of RXRα and EGCG treatment would restore its expression. We indeed found EGCG to restore RXRα activity levels in the human cell lines, in a dose dependent manner and reduced RXRα promoter methylation. EGCG induced methylation changes in several other colon cancer related genes but did not cause a decrease in global methylation. Numerous epidemiological reports have shown the benefits of green tea consumption in reducing colon cancer risk but to date no studies have shown that the risk reduction may be related to the epigenetic restoration by tea polyphenols. Our results show that EGCG modulates the reversal of gene silencing involved in colon carcinogenesis providing a possible avenue for colon cancer prevention and treatment.

Indexed as

Anticarcinogenic AgentsCatechinCell Line, TumorColonic NeoplasmsDNA MethylationGene Expression Regulation, NeoplasticHumansPromoter Regions, GeneticRetinoid X Receptor alphaTeaAnticarcinogenic AgentsCatechinepigallocatechin gallateRetinoid X Receptor alphaTeacolon cancerEGCGepigeneticsmethylationRXRα

Identifiers

PMID27167203
PMCPMC5085231
OpenAlexW2345649975

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.