Evidence map›Paper›PMID 29330282›Full record

ArticleMolecular cancer research : MCR2018

Population-dependent Intron Retention and DNA Methylation in Breast Cancer.

Dongwook Kim, Manu Shivakumar, Seonggyun Han, Michael S Sinclair, Young-Ji Lee, Yonglan Zheng, Olufunmilayo I Olopade, Dokyoon Kim, Younghee Lee

Open access · bronzeAbstract read
In one paragraph

Article in Molecular cancer research : MCR, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.8field-weighted citation impact, top 15% 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

25 citing papers in PubMed, 42 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

9 authors at 1 institution in 1 country.

Dongwook KimDepartment of Biomedical Informatics, University of Utah School of Medicine, Salt Lake City, Utah.
Manu ShivakumarDepartment of Biomedical and Translational Informatics, Geisinger Health System, Danville, Pennsylvania.
Seonggyun HanDepartment of Biomedical Informatics, University of Utah School of Medicine, Salt Lake City, Utah.
Michael S SinclairDepartment of Biomedical Informatics, University of Utah School of Medicine, Salt Lake City, Utah.
Young-Ji LeeDepartment of Health and Community Systems, University of Pittsburgh School of Nursing, Pittsburgh, Pennsylvania.
Yonglan ZhengDepartment of Medicine, University of Chicago, Chicago, Illinois.
Olufunmilayo I OlopadeDepartment of Medicine, University of Chicago, Chicago, Illinois.
Dokyoon KimDepartment of Biomedical and Translational Informatics, Geisinger Health System, Danville, Pennsylvania. younghee.lee@utah.edu dkim@geisinger.edu.
Younghee LeeDepartment of Biomedical Informatics, University of Utah School of Medicine, Salt Lake City, Utah. younghee.lee@utah.edu dkim@geisinger.edu.
University of Chicago · US

Funding

UNIVERSITY OF UTAH MEDICAL INFORMATICS TRAININGT15LM007124 · NLM · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI Karen Louise Eilbeck · 1997 to 2026
$22.0M
Pharmacogenomics of Statin TherapyP50GM115318 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI RISCH, NEIL J. · 2015 to 2019
$14.0M
NIGMS NIH HHS P50 GM115318NLM NIH HHS T15 LM007124
6 · The paper itself

Abstract

Regulation of gene expression by DNA methylation in gene promoter regions is well studied; however, the effects of methylation in the gene body (exons and introns) on gene expression are comparatively understudied. Recently, hypermethylation has been implicated in the inclusion of alternatively spliced exons; moreover, exon recognition can be enhanced by recruiting the methyl-CpG-binding protein (MeCP2) to hypermethylated sites. This study examines whether the methylation status of an intron is correlated with how frequently the intron is retained during splicing using DNA methylation and RNA sequencing data from breast cancer tissue specimens in The Cancer Genome Atlas. Interestingly, hypomethylation of introns is correlated with higher levels of intron expression in mRNA and the methylation level of an intron is inversely correlated with its retention in mRNA from the gene in which it is located. Furthermore, significant population differences were observed in the methylation level of retained introns. In African-American donors, retained introns were not only less methylated compared to European-American donors, but also were more highly expressed. This underscores the need for understanding epigenetic differences in populations and their correlation with breast cancer is an important step toward achieving personalized cancer care.

Indexed as

DNA MethylationIntronsBreast NeoplasmsFemaleGene Expression Regulation, NeoplasticHumansSurvival Analysis

Identifiers

PMID29330282
PMCPMC5835176
OpenAlexW2783399213

What OpenQuestion holds

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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.