Evidence map›Paper›PMID 23368971›Full record

ArticleBMC genomics2013

Genome-wide analysis uncovers high frequency, strong differential chromosomal interactions and their associated epigenetic patterns in E2-mediated gene regulation.

Junbai Wang, Xun Lan, Pei-Yin Hsu, Hang-Kai Hsu, Kun Huang, Jeffrey Parvin, Tim H-M Huang, Victor X Jin

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

22 citing papers in PubMed, 38 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 3 institutions in 2 countries.

Junbai WangDepartment of Pathology, Oslo University Hospital - Norwegian Radium Hospital, Montebello, 0310 Oslo, Norway. junbai.wang@rr-research.no
Xun Lan
Pei-Yin Hsu
Hang-Kai Hsu
Kun Huang
Jeffrey Parvin
Tim H-M Huang
Victor X Jin
The Ohio State University · USThe University of Texas Health Science Center at San Antonio · USNorwegian Cancer Society · NO

Funding

Translational Therapeutics Research Program (TT)P30CA016058 · NCI · OHIO STATE UNIVERSITY · PI Tasleem J Padamsee · 1985 to 2026
$132.3M
Predicting Drug Resistance in Cancer Genomes by DMA Methylation ProfilingU54CA113001 · NCI · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HUANG, TIM H.-M. · 2004 to 2014
$16.1M
Epigenomics of Bisphenol A Exposure and Disease RiskR01ES017594 · NIEHS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI HUANG, TIM H.-M. · 2009 to 2013
$1.8M
NCI NIH HHS P30 CA016058NCI NIH HHS U54 CA113001NIEHS NIH HHS R01 ES017594
6 · The paper itself

Abstract

backgroundAn emerging Hi-C protocol has the ability to probe three-dimensional (3D) architecture and capture chromatin interactions in a genome-wide scale. It provides informative results to address how chromatin organization changes contribute to disease/tumor occurrence and progression in response to stimulation of environmental chemicals or hormones.

resultsIn this study, using MCF7 cells as a model system, we found estrogen stimulation significantly impact chromatin interactions, leading to alteration of gene regulation and the associated histone modification states. Many chromosomal interaction regions at different levels of interaction frequency were identified. In particular, the top 10 hot regions with the highest interaction frequency are enriched with breast cancer specific genes. Furthermore, four types of E2-mediated strong differential (gain- or loss-) chromosomal (intra- or inter-) interactions were classified, in which the number of gain-chromosomal interactions is less than the number of loss-chromosomal interactions upon E2 stimulation. Finally, by integrating with eight histone modification marks, DNA methylation, regulatory elements regions, ERα and Pol-II binding activities, associations between epigenetic patterns and high chromosomal interaction frequency were revealed in E2-mediated gene regulation.

conclusionsThe work provides insight into the effect of chromatin interaction on E2/ERα regulated downstream genes in breast cancer cells.

Indexed as

GenomicsChromatinChromosomes, HumanEpigenesis, GeneticEstradiolEstrogen Receptor alphaEstrogensGene Expression RegulationHumansMCF-7 CellsChromatinEstradiolEstrogen Receptor alphaEstrogens

Identifiers

PMID23368971
PMCPMC3599885
OpenAlexW1985729788

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.