Evidence map›Paper›PMID 30286088›Full record

ArticlePloS one2018

Integrated analysis of DNA methylation profiling and gene expression profiling identifies novel markers in lung cancer in Xuanwei, China.

Juan Wang, Yong Duan, Qing-He Meng, Rong Gong, Chong Guo, Ying Zhao, Yanliang Zhang

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.1field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 30 citations in OpenAlex.

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  6. Medicina (Kaunas, Lithuania) · 2023
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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

7 authors at 2 institutions in 2 countries.

Juan WangDepartment of Clinical Laboratory, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Yong DuanDepartment of Clinical Laboratory, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Qing-He MengDepartment of Laboratory Medicine, the University of Texas MD Anderson Cancer Center, Houston, Texas, United States of America.
Rong GongDepartment of Clinical Laboratory, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Chong GuoDepartment of Clinical Laboratory, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Ying ZhaoDepartment of Clinical Laboratory, First Affiliated Hospital of Kunming Medical University, Kunming, China.
Yanliang ZhangDepartment of Clinical Laboratory, First Affiliated Hospital of Kunming Medical University, Kunming, China.ORCID 0000-0002-0302-0504
Kunming Medical University · CNThe University of Texas MD Anderson Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAberrant DNA methylation occurs frequently in cancer. The aim of this study was to identify novel methylation markers in lung cancer in Xuanwei, China, through integrated genome-wide DNA methylation and gene expression studies.

methodsDifferentially methylated regions (DMRs) and differentially expressed genes (DEGs) were detected on 10 paired lung cancer tissues and noncancerous lung tissues by methylated DNA immunoprecipitation combined with microarray (MeDIP-chip) and gene expression microarray analyses, respectively. Integrated analysis of DMRs and DEGs was performed to screen out candidate methylation-related genes. Both methylation and expression changes of the candidate genes were further validated and analyzed.

resultsCompared with normal lung tissues, lung cancer tissues expressed a total of 6,899 DMRs, including 5,788 hypermethylated regions and 1,111 hypomethylated regions. Integrated analysis of DMRs and DEGs identified 45 tumor-specific candidate genes: 38 genes whose DMRs were hypermethylated and expression was downregulated, and 7 genes whose DMRs were hypomethylated and expression was upregulated. The methylation and expression validation results identified 4 candidate genes (STXBP6, BCL6B, FZD10, and HSPB6) that were significantly hypermethylated and downregulated in most of the tumor tissues compared with the noncancerous lung tissues.

conclusionsThis integrated analysis of genome-wide DNA methylation and gene expression in lung cancer in Xuanwei revealed several genes regulated by promoter methylation that have not been described in lung cancer before. These results provide new insight into the carcinogenesis of lung cancer in Xuanwei and represent promising new diagnostic and therapeutic targets.

Indexed as

Epigenesis, GeneticAdultBiomarkers, TumorChinaCpG IslandsDNA MethylationFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansLung NeoplasmsMaleMiddle AgedNeoplasm ProteinsOligonucleotide Array Sequence AnalysisPromoter Regions, GeneticBiomarkers, TumorNeoplasm Proteins

Identifiers

PMID30286088
PMCPMC6171826
OpenAlexW2895504326

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LicenceCC BY
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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.