Evidence map›Paper›PMID 21724842›Full record

ArticleGenome research2011

Deep sequencing reveals distinct patterns of DNA methylation in prostate cancer.

Jung H Kim, Saravana M Dhanasekaran, John R Prensner, Xuhong Cao, Daniel Robinson, Shanker Kalyana-Sundaram, Christina Huang, Sunita Shankar, Xiaojun Jing, Matthew Iyer and 11 more

Open access · bronzeAbstract read
In one paragraph

Article in Genome research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 114 papers, 5 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
114citing papers in PubMed, 5 pooled it
–field-weighted citation impact
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

114 citing papers in PubMed, 5 syntheses or guidelines pooled it, 182 citations in OpenAlex.

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  20. Targeting the methionine addiction of cancer.American journal of cancer research · 2022
    Review

54 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

21 authors at 3 institutions in 3 countries.

Jung H KimMichigan Center for Translational Pathology, University of Michigan Medical School, Ann Arbor, MI 48109, USA.
Saravana M Dhanasekaran
John R Prensner
Xuhong Cao
Daniel Robinson
Shanker Kalyana-Sundaram
Christina Huang
Sunita Shankar
Xiaojun Jing
Matthew Iyer
Ming Hu
Lee Sam
Catherine Grasso
Christopher A Maher
Nallasivam Palanisamy
Rohit Mehra
Hal D Kominsky
Javed Siddiqui
Jindan Yu
Zhaohui S Qin
Arul M Chinnaiyan
University of Michigan · USEmory University · USPalmetto Hematology Oncology · US

Funding

VACCINIA PSA FOR ANDROGEN-MODULATED POST-SURGICAL RECURRENCE OF PROSTATE CANCERP50CA069568 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI COONEY, KATHLEEN A · 1995 to 2013
$31.3M
Nation Center- Integrative Biomedical Informatics(RMI)U54DA021519 · NIDA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ATHEY, BRIAN DAVID · 2005 to 2010
$21.3M
Training Program in Tumor MicroenvironmentT32CA009676 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Maria G Castro, Analisa Virginia DiFeo · 1992 to 2026
$7.3M
Epitomic Biomarkers of Prostate CancerU01CA111275 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M, RUBIN, MARK A. · 2004 to 2015
$6.8M
Molecuar Sub-typing of Prostate Cancer Based on Recurrent Gene FusionsR01CA132874 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI CHINNAIYAN, ARUL M · 2009 to 2013
$1.2M
Model-Based Methods for Analyzing ChIP Sequencing DataR01HG005119 · NHGRI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI QIN, ZHAOHUI · 2009 to 2012
$1.2M
The Role of beta-adrenergic Signaling in Prostate CancerR00CA129565 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI YU, JINDAN · 2010 to 2012
$732k
The Role of beta-adrenergic Signaling in Prostate CancerK99CA129565 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YU, JINDAN · 2008 to 2009
$310k
Howard Hughes Medical InstituteNCI NIH HHS 1K99CA129565-01A1NCI NIH HHS CA009676-18NCI NIH HHS K99 CA129565NCI NIH HHS P50 CA069568NCI NIH HHS P50CA69568NCI NIH HHS R00 CA129565NCI NIH HHS R01 CA132874NCI NIH HHS R01CA132874NCI NIH HHS T32 CA009676NCI NIH HHS U01 CA111275NHGRI NIH HHS R01 HG005119NHGRI NIH HHS R01HG005119NIDA NIH HHS U54 DA021519
6 · The paper itself

Abstract

Beginning with precursor lesions, aberrant DNA methylation marks the entire spectrum of prostate cancer progression. We mapped the global DNA methylation patterns in select prostate tissues and cell lines using MethylPlex-next-generation sequencing (M-NGS). Hidden Markov model-based next-generation sequence analysis identified ∼68,000 methylated regions per sample. While global CpG island (CGI) methylation was not differential between benign adjacent and cancer samples, overall promoter CGI methylation significantly increased from ~12.6% in benign samples to 19.3% and 21.8% in localized and metastatic cancer tissues, respectively (P-value < 2 × 10(-16)). We found distinct patterns of promoter methylation around transcription start sites, where methylation occurred not only on the CGIs, but also on flanking regions and CGI sparse promoters. Among the 6691 methylated promoters in prostate tissues, 2481 differentially methylated regions (DMRs) are cancer-specific, including numerous novel DMRs. A novel cancer-specific DMR in the WFDC2 promoter showed frequent methylation in cancer (17/22 tissues, 6/6 cell lines), but not in the benign tissues (0/10) and normal PrEC cells. Integration of LNCaP DNA methylation and H3K4me3 data suggested an epigenetic mechanism for alternate transcription start site utilization, and these modifications segregated into distinct regions when present on the same promoter. Finally, we observed differences in repeat element methylation, particularly LINE-1, between ERG gene fusion-positive and -negative cancers, and we confirmed this observation using pyrosequencing on a tissue panel. This comprehensive methylome map will further our understanding of epigenetic regulation in prostate cancer progression.

Indexed as

DNA MethylationCell Line, TumorCpG IslandsDNA, NeoplasmEpigenomicsEpithelial CellsGene Expression ProfilingGene LibraryHigh-Throughput Nucleotide SequencingHumansMaleMarkov ChainsNeoplasm MetastasisOligonucleotide Array Sequence AnalysisPolymerase Chain ReactionPromoter Regions, GeneticDNA, Neoplasm

Identifiers

PMID21724842
PMCPMC3129246
OpenAlexW2114884175

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.