Evidence map›Paper›PMID 31608179›Full record

ArticlePeerJ2019

Integrative transcriptome data mining for identification of core lncRNAs in breast cancer.

Xiaoming Zhang, Jing Zhuang, Lijuan Liu, Zhengguo He, Cun Liu, Xiaoran Ma, Jie Li, Xia Ding, Changgang Sun

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2019. 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
1.9field-weighted citation impact, top 15% 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, 39 citations in OpenAlex.

  1. Review
  2. Article
  3. A novel LINC00478 serves as a tumor suppressor in endometrial carcinoma progression.Journal of cancer research and clinical oncology · 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

9 authors at 5 institutions in 2 countries.

Xiaoming ZhangCollege of Traditional Chinese Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Jing ZhuangDepartment of Oncology, Affiliated Hospital of Weifang Medical University, Weifang, Shandong, China.
Lijuan LiuDepartment of Oncology, Weifang Traditional Chinese Hospital, Weifang, Shandong, China.
Zhengguo HeHealth Science Center, Columbus Technical College, Columbus, GA, the United States of America.
Cun LiuCollege of First Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Xiaoran MaCollege of First Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Jie LiCollege of First Clinical Medicine, Shandong University of Traditional Chinese Medicine, Jinan, Shandong, China.
Xia DingSchool of Traditional Chinese Medicine, Beijing University of Chinese Medicine, Beijing, China.
Changgang SunDepartment of Oncology, Affiliated Hospital of Weifang Medical University, Weifang, Shandong, China.
Shandong University of Traditional Chinese Medicine · CNWeifang Medical University · CNBeijing University of Chinese Medicine · CNColumbus Technical College · USWeifang Chinese Medicine Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCumulative evidence suggests that long non-coding RNAs (lncRNAs) play an important role in tumorigenesis. This study aims to identify lncRNAs that can serve as new biomarkers for breast cancer diagnosis or screening.

methodsFirst, the linear fitting method was used to identify differentially expressed genes from the breast cancer RNA expression profiles in The Cancer Genome Atlas (TCGA). Next, the diagnostic value of all differentially expressed lncRNAs was evaluated using a receiver operating characteristic (ROC) curve. Then, the top ten lncRNAs with the highest diagnostic value were selected as core genes for clinical characteristics and prognosis analysis. Furthermore, core lncRNA-mRNA co-expression networks based on weighted gene co-expression network analysis (WGCNA) were constructed, and functional enrichment analysis was performed using the Database for Annotation, Visualization and Integrated Discovery (DAVID). The differential expression level and diagnostic value of core lncRNAs were further evaluated by using independent data set from Gene Expression Omnibus (GEO). Finally, the expression status and prognostic value of core lncRNAs in various tumors were analyzed based on Gene Expression Profiling Interactive Analysis (GEPIA).

resultsSeven core lncRNAs (LINC00478, PGM5-AS1, AL035610.1, MIR143HG, RP11-175K6.1, AC005550.4, and MIR497HG) have good single-factor diagnostic value for breast cancer. AC093850.2 has a prognostic value for breast cancer. AC005550.4 and MIR497HG can better distinguish breast cancer patients in early-stage from the advanced-stage. Low expression of MAGI2-AS3, LINC00478, AL035610.1, MIR143HG, and MIR145 may be associated with lymph node metastasis in breast cancer.

conclusionOur study provides candidate biomarkers for the diagnosis and prognosis of breast cancer, as well as a bioinformatics basis for the further elucidation of the molecular pathological mechanism of breast cancer.

Indexed as

BioinformaticsBiomarkersBreast cancerlncRNAWGCNA

Identifiers

PMID31608179
PMCPMC6786248
OpenAlexW2977705663

What OpenQuestion holds

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LicenceCC BY-NC
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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.