Evidence map›Paper›PMID 18413733›Full record

ArticleCancer research2008

Genome-wide promoter analysis uncovers portions of the cancer methylome.

Mohammad Obaidul Hoque, Myoung Sook Kim, Kimberly Laskie Ostrow, Junwei Liu, G Bea A Wisman, Hannah Lui Park, Maria Luana Poeta, Carmen Jeronimo, Rui Henrique, Agnes Lendvai and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Cancer research, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 84 papers.

0numbers the graph read from it
0cells of the map it votes in
84citing papers in PubMed
7.2field-weighted citation impact, top 2% 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

84 citing papers in PubMed, 150 citations in OpenAlex.

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  17. Cancer prevention research (Philadelphia, Pa.) · 2020
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24 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

20 authors at 6 institutions in 5 countries.

Mohammad Obaidul HoqueDepartment of Otolaryngology-Head and Neck Surgery, The Johns Hopkins School of Medicine, Baltimore, Maryland 21231, USA.
Myoung Sook Kim
Kimberly Laskie Ostrow
Junwei Liu
G Bea A Wisman
Hannah Lui Park
Maria Luana Poeta
Carmen Jeronimo
Rui Henrique
Agnes Lendvai
Ed Schuuring
Shahnaz Begum
Eli Rosenbaum
Maté Ongenaert
Keishi Yamashita
Joseph Califano
William Westra
Ate G J van der Zee
Wim Van Criekinge
David Sidransky
Gynecologic Oncology Group · USJohns Hopkins University · USUniversidade do Porto · PTGhent University · BEUniversità Campus Bio-Medico · ITUniversity Medical Center Groningen · NL

Funding

INTEGRATED DEVELOPMENT OF NOVEL MOLECULAR MARKERSU01CA084986 · NCI · JOHNS HOPKINS UNIVERSITY · PI SIDRANSKY, DAVID · 1999 to 2014
$33.8M
NCI NIH HHS U01 CA084986NCI NIH HHS U01-CA84986
6 · The paper itself

Abstract

DNA methylation has a role in mediating epigenetic silencing of CpG island genes in cancer and other diseases. Identification of all gene promoters methylated in cancer cells "the cancer methylome" would greatly advance our understanding of gene regulatory networks in tumorigenesis. We previously described a new method of identifying methylated tumor suppressor genes based on pharmacologic unmasking of the promoter region and detection of re-expression on microarray analysis. In this study, we modified and greatly improved the selection of candidates based on new promoter structure algorithm and microarray data generated from 20 cancer cell lines of 5 major cancer types. We identified a set of 200 candidate genes that cluster throughout the genome of which 25 were previously reported as harboring cancer-specific promoter methylation. The remaining 175 genes were tested for promoter methylation by bisulfite sequencing or methylation-specific PCR (MSP). Eighty-two of 175 (47%) genes were found to be methylated in cell lines, and 53 of these 82 genes (65%) were methylated in primary tumor tissues. From these 53 genes, cancer-specific methylation was identified in 28 genes (28 of 53; 53%). Furthermore, we tested 8 of the 28 newly identified cancer-specific methylated genes with quantitative MSP in a panel of 300 primary tumors representing 13 types of cancer. We found cancer-specific methylation of at least one gene with high frequency in all cancer types. Identification of a large number of genes with cancer-specific methylation provides new targets for diagnostic and therapeutic intervention, and opens fertile avenues for basic research in tumor biology.

Indexed as

DNA MethylationGenome, HumanPromoter Regions, GeneticAntimetabolites, AntineoplasticBiotinylationBromodeoxyuridineCell Line, TumorGene Expression Regulation, NeoplasticHumansModels, GeneticNeoplasmsOligonucleotide Array Sequence AnalysisAntimetabolites, AntineoplasticBromodeoxyuridine

Identifiers

PMID18413733
PMCPMC3102297
OpenAlexW2150823666

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.