Evidence map›Paper›PMID 34368351›Full record

ArticleBioMed research international2021

Multiomics Profiling and Clustering of Low-Grade Gliomas Based on the Integrated Stress Status.

Xiaolin Ren, Xin Chen, Chen Zhu, Anhua Wu

Open access · hybridAbstract read
In one paragraph

Article in BioMed research international, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 43% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. Article
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

4 authors at 1 institution in 1 country.

Xiaolin RenDepartment of Neurosurgery, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.ORCID https://orcid.org/0000-0003-0369-5007
Xin ChenDepartment of Neurosurgery, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.ORCID https://orcid.org/0000-0001-6217-8769
Chen ZhuDepartment of Neurosurgery, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.ORCID https://orcid.org/0000-0001-5389-7622
Anhua WuDepartment of Neurosurgery, The First Affiliated Hospital of China Medical University, Shenyang, Liaoning, China.ORCID https://orcid.org/0000-0002-3402-1884
First Hospital of China Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlthough the prognosis of low-grade glioma is better than that of glioblastoma, there are still some groups with poor prognosis. The integrated stress response contributes to the malignant progress of tumors. As there had limited research focused on the integrated stress status in LGG, it is urgent to profile and reclassify LGG based on the integrated stress response.

methodsInformation of glioma patients was obtained from the Chinese Glioma Genome Atlas, The Cancer Genome Atlas, and the GSE16011 cohorts. Statistical analyses were conducted using GraphPad Prism 8 and R language.

resultsWe summarized and quantified four types of integrated stress responses. Relationships between these four types of stress states and the clinical characteristics were analyzed in low-grade glioma. We then reclassified the patients based on these four scores and found that cluster 2 had the worst prognosis, while cluster 1 had the best prognosis. We also established an accurate integrated stress response risk signature for predicting cluster 2. We found that immune response and suppressive immune cell components were more enriched in the high-risk group. We also profiled the genomic differences between the low- and high-risk groups, including the nonmissense mutation of driver genes and the copy number variations.

conclusionLow-grade glioma patients were divided into three clusters based on the integrated stress status, with cluster 2 exhibiting malignant transformation trends. The signature adequately reflected the traits of cluster 2, while a high risk score indicated a worse prognosis and an enriched inhibitory immune microenvironment.

Indexed as

GenomicsStress, PhysiologicalBrain NeoplasmsCluster AnalysisDNA Copy Number VariationsGliomaHumansMutationNeoplasm GradingPhenotypeRisk FactorsTumor Microenvironment

Identifiers

PMID34368351
PMCPMC8343268
OpenAlexW3186315102

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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.