Evidence map›Paper›PMID 33790966›Full record

ArticleJournal of oncology2021

Construction of a Prognostic Gene Signature Associated with Immune Infiltration in Glioma: A Comprehensive Analysis Based on the CGGA.

Xiaoxiang Gong, Lingjuan Liu, Jie Xiong, Xingfang Li, Jie Xu, Yangyang Xiao, Jian Li, Xuemei Luo, Dingan Mao, Liqun Liu

Open access · hybridAbstract read
In one paragraph

Article in Journal of oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

10 citing papers in PubMed, 14 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

10 authors at 1 institution in 1 country.

Xiaoxiang GongDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.
Lingjuan LiuDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.
Jie XiongDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.
Xingfang LiDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.
Jie XuDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.
Yangyang XiaoDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.
Jian LiDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.
Xuemei LuoDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.
Dingan MaoDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.
Liqun LiuDepartment of Pediatrics, The Second Xiangya Hospital, Central South University, Changsha 410011, Hunan, China.ORCID https://orcid.org/0000-0002-0322-1664
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTumor microenvironment (TME) is closely related to the progression of glioma and the therapeutic effect of drugs on this cancer. The aim of this study was to develop a signature associated with the tumor immune microenvironment using machine learning.

methodsWe downloaded the transcriptomic and clinical data of glioma patients from the Chinese Glioma Genome Atlas (CGGA) databases (mRNAseq_693). The single-sample Gene Set Enrichment Analysis (ssGSEA) database was used to quantify the relative abundance of immune cells. We divided patients into two different infiltration groups via unsupervised clustering analysis of immune cells and then selected differentially expressed genes (DEGs) between the two groups. Survival-related genes were determined using Cox regression analysis. We next randomly divided patients into a training set and a testing set at a ratio of 7 : 3. By integrating the DEGs into least absolute shrinkage and selection operator (LASSO) regression analysis in the training set, we were able to construct a 15-gene signature, which was validated in the testing and total sets. We further validated the signature in the mRNAseq_325 dataset of CGGA.

resultsWe identified 74 DEGs associated with tumor immune infiltration, 70 of which were significantly associated with overall survival (OS). An immune-related gene signature was established, consisting of 15 key genes: adenosine triphosphate (ATP)-binding cassette subfamily C member 3 (

conclusionWe constructed a stable gene signature associated with immune infiltration to predict the survival rates of glioma patients.

Identifiers

PMID33790966
PMCPMC7984893
OpenAlexW3137279813

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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.