Evidence map›Paper›PMID 19250546›Full record

ArticleBreast cancer research : BCR2009

Methylation of homeobox genes is a frequent and early epigenetic event in breast cancer.

Stella Tommasi, Deborah L Karm, Xiwei Wu, Yun Yen, Gerd P Pfeifer

Open access · goldAbstract read
In one paragraph

Article in Breast cancer research : BCR, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
6.7field-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

81 citing papers in PubMed, 153 citations in OpenAlex.

  1. Article
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  14. Genomics, Epigenetics, and Hearing Loss in Neurofibromatosis Type 2.Otology & neurotology : official publication of the American Otological Society, American Neurotology Society [and] European Academy of Otology and Neurotology · 2020
    Review
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21 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

5 authors at 2 institutions in 1 country.

Stella TommasiDepartment of Cancer Biology, Beckman Research Institute of the City of Hope, Duarte, CA 91010, USA. stommasi@coh.org
Deborah L Karm
Xiwei Wu
Yun Yen
Gerd P Pfeifer
City of Hope · USBeckman Research Institute

Funding

CPG METHYLATION AND MUTATIONR01CA084469 · NCI · CITY OF HOPE/BECKMAN RESEARCH INSTITUTE · PI PFEIFER, GERD P · 2000 to 2013
$4.0M
DNA methylation in cancer genomesR21CA128495 · NCI · BECKMAN RESEARCH INSTITUTE/CITY OF HOPE · PI PFEIFER, GERD P · 2007 to 2008
$465k
NCI NIH HHS CA 084469NCI NIH HHS CA 128495NCI NIH HHS R01 CA084469NCI NIH HHS R21 CA128495
6 · The paper itself

Abstract

introductionAberrant methylation of CpG islands is a hallmark of cancer and occurs at an early stage in breast tumorigenesis. However, its impact on tumor development is not fully determined, and its potential as a diagnostic biomarker remains to be validated. Methylation profiling of invasive breast carcinoma has been largely explored. Conversely, very little and sparse information is available on early-stage breast cancer. To gain insight into the epigenetic switches that may promote and/or contribute to the initial neoplastic events during breast carcinogenesis, we have analyzed the DNA methylation profile of ductal carcinoma in situ, a premalignant breast lesion with a great potential to progress toward invasive carcinoma.

methodsWe have utilized a comprehensive and sensitive array-based DNA mapping technique, the methylated-CpG island recovery assay, to profile the DNA methylation pattern in ductal carcinoma in situ. Differential methylation of CpG islands was compared genome-wide in tumor DNA versus normal DNA utilizing a statistical linear model in the LIMMA software package.

resultsUsing this approach, we have identified 108 significant CpG islands that undergo aberrant DNA methylation in ductal carcinoma in situ and stage I breast tumors, with methylation frequencies greater than or comparable with those of more advanced invasive carcinoma (50% to 93%). A substantial fraction of these hypermethylated CpG islands (32% of the annotated CpG islands) is associated with several homeobox genes, such as the TLX1, HOXB13, and HNF1B genes. Fifty-three percent of the genes hypermethylated in early-stage breast cancer overlap with known Polycomb targets and include homeobox genes and other developmental transcription factors.

conclusionsWe have identified a series of new potential methylation biomarkers that may help elucidate the underlying mechanisms of breast tumorigenesis. More specifically, our results are suggestive of a critical role of homeobox gene methylation in the insurgence and/or progression of breast cancer.

Indexed as

DNA MethylationEpigenesis, GeneticGene Expression Regulation, NeoplasticBreast NeoplasmsCarcinoma, Ductal, BreastCpG IslandsGenome, HumanHomeodomain ProteinsHumansOligonucleotide Array Sequence AnalysisPrognosisPromoter Regions, GeneticHomeodomain Proteins

Identifiers

PMID19250546
PMCPMC2687719
OpenAlexW2035122273

What OpenQuestion holds

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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.