Evidence map›Paper›PMID 31528121›Full record

ArticleCancer cell international2019

Prognostic significance of TOP2A in non-small cell lung cancer revealed by bioinformatic analysis.

Wenxia Ma, Bin Wang, Yaping Zhang, Ziyue Wang, Dan Niu, Siyu Chen, Zhirong Zhang, Ningning Shen, Weixia Han, Xiaoqin Zhang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Cancer cell international, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
4.2field-weighted citation impact, top 5% 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

30 citing papers in PubMed, 52 citations in OpenAlex.

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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

12 authors at 1 institution in 1 country.

Wenxia Ma *Department of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Bin Wang *Department of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Yaping ZhangDepartment of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Ziyue WangDepartment of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Dan NiuDepartment of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Siyu ChenDepartment of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Zhirong ZhangDepartment of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Ningning ShenDepartment of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Weixia HanDepartment of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Xiaoqin ZhangDepartment of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Rong WeiDepartment of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.
Chen Wang *Department of Pathology, The Second Hospital of ShanXi Medical University, No. 382 WuYi Road, Tai Yuan, 030000 Shanxi China.ORCID 0000-0002-4919-9677
Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLung cancer has been a common malignant tumor with a leading cause of morbidity and mortality, current molecular targets are woefully lacking comparing to the highly progressive cancer. The study is designed to identify new prognostic predictors and potential gene targets based on bioinformatic analysis of Gene Expression Omnibus (GEO) database.

methodsFour cDNA expression profiles GSE19188, GSE101929, GSE18842 and GSE33532 were chosen from GEO database to analyze the differently expressed genes (DEGs) between non-small cell lung cancer (NSCLC) and normal lung tissues. After the DEGs functions were analyzed, the protein-protein interaction network (PPI) of DEGs were constructed, and the core gene in the network which has high connectivity degree with other genes was identified. We analyzed the association of the gene with the development of NSCLC as well as its prognosis. Lastly we explored the conceivable signaling mechanism of the gene regulation during the development of NSCLC.

resultsA total of 92 up regulated and 214 down regulated DEGs were shared in four cDNA expression profiles. Based on their PPI network, TOP2A was connected with most of other genes and was selected for further analysis. Kaplan-Meier overall survival analysis (OS) revealed that TOP2A was associated with worse NSCLC patients survival. And both GEPIA analysis and immunohistochemistry experiment (IHC) confirmed that TOP2A was aberrant gain of expression in cancer comparing to normal tissues. The clinical significance of TOP2A and probable signaling pathways it involved in were further explored, and a positive correlation between TOP2A and TPX2 expression was found in lung cancer tissues.

conclusionUsing bioinformatic analysis, we revealed that TOP2A could be adopted as a prognostic indicator of NSCLC and it potentially regulate cancer development through co-work with TPX2. However, more detailed experiments are needed to clarify its drug target role in clinical medical use.

Indexed as

BiomarkerDifferent expressed genes (DEGs)GEO databaseNon-small cell lung cancer (NSCLC)Protein–protein interaction network (PPI)Survival analysisTOP2A

Identifiers

PMID31528121
PMCPMC6737627
OpenAlexW2972697509

What OpenQuestion holds

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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.