Evidence map›Paper›PMID 37205199›Full record

ArticleFrontiers in oncology2023

Oncogenic role and drug sensitivity of ETV4 in human tumors: a pan-cancer analysis.

Rui Zhang, Yanfang Peng, Zhe Gao, Jing Qian, Kang Yang, Xinfa Wang, Wenjing Lu, Yongjie Zhu, Dezhi Qiu, Tong Jin and 3 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.6field-weighted citation impact, top 16% 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

9 citing papers in PubMed, 6 citations in OpenAlex.

  1. Article
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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

13 authors at 4 institutions in 1 country.

Rui ZhangDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Yanfang PengNanjing Drum Tower Hospital, The Affiliated Hospital of Nanjing University Medical School, Nanjing, Jiangsu, China.
Zhe GaoDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Jing QianDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Kang YangDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Xinfa WangDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Wenjing LuDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Yongjie ZhuDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Dezhi QiuDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Tong JinDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Gang WangDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Junping HeDepartment of Neurosurgery, Children's Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Ning LiuDepartment of Neurosurgery, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu, China.
Second Affiliated Hospital of Nanjing Medical University · CNJiangsu Province Hospital · CNNanjing Drum Tower Hospital · CNNanjing Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Increasing evidence supports a relationship between E twenty-six variant transcription factor 4 (ETV4) and several cancers, but no pan-cancer analysis has been reported. Methods: The present study surveyed the effects of ETV4 on cancer using RNA sequencing data obtained from The Cancer Genome Atlas and GTEx, and further explored its role in drug sensitivity using data from Cellminer. Differential expression analyses were conducted for multiple cancers using R software. Cox regression and survival analysis were employed to calculate correlations between ETV4 levels and survival outcomes in multiple cancers using the online tool Sangerbox. ETV4 expression was also compared with immunity, heterogeneity, stemness, mismatch repair genes, and DNA methylation among different cancers. Results: ETV4 was found to be significantly upregulated in 28 tumors. Upregulation of ETV4 was associated with poor overall survival, progression free interval, disease-free-interval, and disease specific survival in several cancer types. Expression of ETV4 was also remarkably correlated with immune cell infiltration, tumor heterogeneity, mismatch repair gene expression, DNA methylation, and tumor stemness. Furthermore, ETV4 expression seemed to affect sensitivity to a number of anticancer drugs. Conclusions: These results suggest that ETV4 may be useful as a prognostic factor and therapeutic target.

Indexed as

drug sensitivityETV4immunitymicroenvironmentpancancerprognostic

Identifiers

PMID37205199
PMCPMC10185867
OpenAlexW4367852523

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.