Evidence map›Paper›PMID 34899682›Full record

ArticleFrontiers in immunology2021

Identification of Immune-Related lncRNA Prognostic Signature and Molecular Subtypes for Glioblastoma.

Wanli Yu, Yanan Ma, Wenbin Hou, Fang Wang, Wan Cheng, Feng Qiu, Pengfei Wu, Guohua Zhang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in immunology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
3.6field-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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 55 citations in OpenAlex.

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  15. The mFrontiers in oncology · 2025
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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

8 authors at 6 institutions in 1 country.

Wanli YuDepartment of Neurosurgery, Gaoxin Hospital of The First Affiliated Hospital of Nanchang University, Nanchang, China.
Yanan MaLaboratory of Medical Genetics, Harbin Medical University, Harbin, China.
Wenbin HouDepartment of Urology, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Fang WangDepartment of Neurosurgery, The Second Affiliated Hospital of Harbin Medical University, Harbin, China.
Wan ChengThe Laboratory of Artificial Intelligence and Bigdata in Ophthalmology, The Affiliated Eye Hospital of Nanjing Medical University, Nanjing, China.
Feng QiuOncology Department, Gaoxin Hospital of The First Affiliated Hospital of Nanchang University, Nanchang, China.
Pengfei WuDepartment of Neurosurgery, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Guohua ZhangCentral Laboratory, Gaoxin Hospital of The First Affiliated Hospital of Nanchang University, Nanchang, China.
Nanchang University · CNSecond Affiliated Hospital of Harbin Medical University · CNFirst Affiliated Hospital of Nanchang University · CNHarbin Medical University · CNNanjing Medical University · CNUniversity of Science and Technology of China · CN

Funding

Intramuscular Mechanisms of Cancer CachexiaR01AR067319 · NIAMS · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LI, YI-PING · 2015 to 2019
$2.2M
NIAMS NIH HHS R01 AR067319
6 · The paper itself

Abstract

Background: Glioblastoma multiforme (GBM) is extensively genetically and transcriptionally heterogeneous, which poses challenges for classification and management. Long noncoding RNAs (lncRNAs) play a critical role in the development and progression of GBM, especially in tumor-associated immune processes. Therefore, it is necessary to develop an immune-related lncRNAs (irlncRNAs) signature. Methods: Univariate and multivariate Cox regression analyses were utilized to construct a prognostic model. GBM-specific CeRNA and PPI network was constructed to predict lncRNAs targets and evaluate the interactions of immune mRNAs translated proteins. GO and KEGG pathway analyses were used to show the biological functions and pathways of CeRNA network-related immunity genes. Consensus Cluster Plus analysis was used for GBM gene clustering. Then, we evaluated GBM subtype-specific prognostic values, clinical characteristics, genes and pathways, immune infiltration access single cell RNA-seq data, and chemotherapeutics efficacy. The hub genes were finally validated. Results: A total of 17 prognostically related irlncRNAs were screened to build a prognostic model signature based on six key irlncRNAs. Based on GBM-specific CeRNAs and enrichment analysis, Conclusion: Construction of lncRNAs risk model and identification of GBM subtypes based on 17 irlncRNAs, which suggesting that irlncRNAs had the promising potential for clinical immunotherapy of GBM.

Indexed as

Biomarkers, TumorBrain NeoplasmsGene Regulatory NetworksGlioblastomaHumansMultigene FamilyPrognosisRNA, Long NoncodingTranscriptomeBiomarkers, TumorRNA, Long Noncodingbiomarkerglioblastomaimmune infiltrationimmune-related lncRNAsprognostic signature

Identifiers

PMID34899682
PMCPMC8657607
OpenAlexW3216968957

What OpenQuestion holds

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LicenceCC BY
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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.