Evidence map›Paper›PMID 32373154›Full record

ArticleFrontiers in genetics2020

Genome-Wide Analysis of Methylation-Driven Genes and Identification of an Eight-Gene Panel for Prognosis Prediction in Breast Cancer.

Yanshen Kuang, Ying Wang, Wanli Zhai, Xuning Wang, Bingdong Zhang, Maolin Xu, Shaohua Guo, Mu Ke, Baoqing Jia, Hongyi Liu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.2field-weighted citation impact, top 23% 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

12 citing papers in PubMed, 21 citations in OpenAlex.

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  5. ctDNACancer management and research · 2024
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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

10 authors at 3 institutions in 1 country.

Yanshen KuangDepartment of General Surgery, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
Ying WangState Key Laboratory of Membrane Biology, School of Medicine, Tsinghua University, Beijing, China.
Wanli ZhaiState Key Laboratory of Membrane Biology, School of Medicine, Tsinghua University, Beijing, China.
Xuning WangDepartment of General Surgery, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
Bingdong ZhangDepartment of General Surgery, Beijing Shijitan Hospital, Capital Medical University, Beijing, China.
Maolin XuDepartment of General Surgery, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
Shaohua GuoDepartment of General Surgery, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
Mu KeDepartment of General Surgery, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
Baoqing JiaDepartment of General Surgery, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
Hongyi LiuDepartment of General Surgery, The First Medical Center, Chinese PLA General Hospital, Beijing, China.
Chinese PLA General Hospital · CNTsinghua University · CNCapital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAberrant DNA methylation is a crucial epigenetic regulator that is closely related to the occurrence and development of various cancers, including breast cancer (BC). The present study aimed to identify a novel methylation-based prognosis biomarker panel by integrally analyzing gene expression and methylation patterns in BC patients.

methodsDNA methylation and gene expression data of breast cancer (BRCA) were downloaded from The Cancer Genome Atlas (TCGA). R packages, including ChAMP, SVA, and MethylMix, were applied to identify the unique methylation-driven genes. Subsequently, these genes were subjected to Metascape for GO analysis. Univariant Cox regression was used to identify survival-related genes among the methylation-driven genes. Robust likelihood-based survival modeling was applied to define the prognosis markers. An independent data set (GSE72308) was used for further validation of our risk score system.

resultsA total of 879 DNA methylation-driven genes were identified from 765 BC patients. In the discovery cohort, we identified 50 survival-related methylation-driven genes. Finally, we built an eight-methylation-driven gene panel that serves as prognostic predictors.

conclusionsOur analysis of transcriptome and methylome variations associated with the survival status of BC patients provides a further understanding of basic biological processes and a basis for the genetic etiology in BC.

Indexed as

breast cancerDNA methylationepigeneticsintegrative analysisprognosis biomarker

Identifiers

PMID32373154
PMCPMC7186397
OpenAlexW3018777925

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Registered trials

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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.