Evidence map›Paper›PMID 41425851›Full record

ArticleInternational journal of genomics2025

CLDN22 Serves as a Novel Prognostic Biomarker and Immunotherapy Response Predictor in Gliomas: A Comprehensive Multiomics Analysis.

Hui Zheng, Jingsong Cheng, Jialin Liu, Guodong Liu, Ronglun Dang, Rugang Luo, Jinhe Lou

Abstract read
In one paragraph

Article in International journal of genomics, 2025. 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
–field-weighted citation impact
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.

  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

7 authors.

Hui ZhengDepartment of Neurosurgery, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China, cqmu.edu.cn.ORCID https://orcid.org/0009-0002-4475-5942
Jingsong ChengDepartment of Neurosurgery, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China, cqmu.edu.cn.
Jialin LiuDepartment of Neurosurgery, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China, cqmu.edu.cn.
Guodong LiuDepartment of Neurosurgery, The Second Affiliated Hospital of Chongqing Medical University, Chongqing, China, cqmu.edu.cn.ORCID https://orcid.org/0000-0002-8048-2243
Ronglun DangDepartment of Neurosurgery, Hami Central Hospital, Hami, Xinjiang, China.
Rugang LuoDepartment of Neurosurgery, Renhuai People's Hospital, Renhuai, Guizhou, China.
Jinhe LouDepartment of Geriatrics, The Thirteenth People's Hospital of Chongqing/Chongqing Geriatrics Hospital, Chongqing, China.ORCID https://orcid.org/0000-0002-1315-7889

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The claudin gene family plays crucial roles in cancer biology, yet their comprehensive molecular characteristics and clinical implications in gliomas remain unclear. Methods: Multiomics data from The Cancer Genome Atlas (TCGA) were analyzed, and differential expression analysis was performed between glioma and normal samples. Consensus clustering was applied to identify molecular subtypes. Multiple machine learning algorithms, including least absolute shrinkage and selection operator (LASSO), extreme gradient boosting (XGBoost), Boruta, prediction analysis of microarrays (PAMR), and random forest, were employed for feature selection. Immune characteristics were evaluated using Estimation of STromal and Immune cells in MAlignant Tumors using Expression data (ESTIMATE), cell-type enrichment analysis by gene expression signatures (xCell), and Cell-type Identification By Estimating Relative Subsets Of RNA Transcripts (CIBERSORT) algorithms. Drug sensitivity analysis was conducted using the Genomics of Drug Sensitivity in Cancer (GDSC) database. Functional enrichment analysis was performed based on Gene Ontology (GO) terms and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways. Results: We identified distinct regulatory patterns of claudin family genes involving CNV and DNA methylation. Consensus clustering revealed two molecular subtypes with significant differences in survival ( Conclusion: Our comprehensive analysis establishes CLDN22 as a novel prognostic and predictive biomarker in gliomas with significant implications for patient stratification and therapeutic decision-making. These findings provide new insights into glioma biology and potential therapeutic strategies, though further experimental validation is warranted.

Indexed as

claudin genegliomasTCGAtumor microenvironment

Identifiers

PMID41425851
PMCPMC12717531

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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.