Evidence map›Paper›PMID 25706888›Full record

ArticlePloS one2015

Hierarchical clustering of breast cancer methylomes revealed differentially methylated and expressed breast cancer genes.

I-Hsuan Lin, Dow-Tien Chen, Yi-Feng Chang, Yu-Ling Lee, Chia-Hsin Su, Ching Cheng, Yi-Chien Tsai, Swee-Chuan Ng, Hsiao-Tan Chen, Mei-Chen Lee and 6 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

19 citing papers in PubMed, 35 citations in OpenAlex.

  1. MRI phenotypes of the brain are related to future stroke and mortality in patients with manifest arterial disease: The SMART-MR study.Journal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2020
    Trial
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  6. Bioinformatics advances · 2024
    Article
  7. Machine Learning in Epigenomics: Insights into Cancer Biology and Medicine.Biochimica et biophysica acta. Reviews on cancer · 2021
    Review
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  14. High-Resolution Bisulfite-Sequencing of Peripheral Blood DNA Methylation in Early-Onset and Familial Risk Breast Cancer Patients.Clinical cancer research : an official journal of the American Association for Cancer Research · 2019
    Article
  15. Article
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  18. Large-scale analysis ofClinical epigenetics · 2018
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  19. Article
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

16 authors at 3 institutions in 1 country.

I-Hsuan LinVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan; Institute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan.
Dow-Tien ChenVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan.
Yi-Feng ChangInstitute of Biomedical Informatics, National Yang-Ming University, Taipei, Taiwan.
Yu-Ling LeeInstitute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan.
Chia-Hsin SuInstitute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan.
Ching ChengInstitute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan.
Yi-Chien TsaiInstitute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan.
Swee-Chuan NgVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan.
Hsiao-Tan ChenVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan.
Mei-Chen LeeVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan.
Hong-Wei ChenVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan.
Shih-Hui SuenVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan.
Yu-Cheng ChenVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan.
Tze-Tze LiuVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan.
Chuan-Hsiung ChangCenter for Systems and Synthetic Biology, National Yang-Ming University, Taipei, Taiwan; Institute of Biomedical Informatics, National Yang-Ming University, Taipei, Taiwan.
Ming-Ta HsuVGH-YM Genome Center, National Yang-Ming University, Taipei, Taiwan; Institute of Biochemistry and Molecular Biology, National Yang-Ming University, Taipei, Taiwan.
National Yang Ming Chiao Tung University · TWInstitute of Molecular Biology, Academia Sinica · TWNational Yang Ming Chiao Tung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oncogenic transformation of normal cells often involves epigenetic alterations, including histone modification and DNA methylation. We conducted whole-genome bisulfite sequencing to determine the DNA methylomes of normal breast, fibroadenoma, invasive ductal carcinomas and MCF7. The emergence, disappearance, expansion and contraction of kilobase-sized hypomethylated regions (HMRs) and the hypomethylation of the megabase-sized partially methylated domains (PMDs) are the major forms of methylation changes observed in breast tumor samples. Hierarchical clustering of HMR revealed tumor-specific hypermethylated clusters and differential methylated enhancers specific to normal or breast cancer cell lines. Joint analysis of gene expression and DNA methylation data of normal breast and breast cancer cells identified differentially methylated and expressed genes associated with breast and/or ovarian cancers in cancer-specific HMR clusters. Furthermore, aberrant patterns of X-chromosome inactivation (XCI) was found in breast cancer cell lines as well as breast tumor samples in the TCGA BRCA (breast invasive carcinoma) dataset. They were characterized with differentially hypermethylated XIST promoter, reduced expression of XIST, and over-expression of hypomethylated X-linked genes. High expressions of these genes were significantly associated with lower survival rates in breast cancer patients. Comprehensive analysis of the normal and breast tumor methylomes suggests selective targeting of DNA methylation changes during breast cancer progression. The weak causal relationship between DNA methylation and gene expression observed in this study is evident of more complex role of DNA methylation in the regulation of gene expression in human epigenetics that deserves further investigation.

Indexed as

DNA MethylationGenes, NeoplasmMultigene FamilyBreast NeoplasmsFemaleHumansPromoter Regions, GeneticX Chromosome Inactivation

Identifiers

PMID25706888
PMCPMC4338251
OpenAlexW2004491550

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.