Evidence map›Paper›PMID 39993959›Full record

ArticleJournal of cellular and molecular medicine2025

Integrative Disulfidptosis-Based Risk Assessment for Prognostic Stratification and Immune Profiling in Glioma.

Xiaowang Niu, Guangzhao Li, Ulf D Kahlert, Leili Ding, Jing Zheng, Chen Li, Wenjie Shi, Lifen Huang, Zhengquan Yu

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

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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

9 authors.

Xiaowang NiuDepartment of Neurosurgery, The First Affiliated Hospital of Soochow University, Suzhou, China.
Guangzhao LiDepartment of Neurosurgery, Hefei First People's Hospital, Hefei, China.
Ulf D KahlertMolecular and Experimental Surgery, Clinic for General-, Visceral -, Vascular- and Transplantation Surgery, University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.
Leili DingMolecular and Experimental Surgery, Clinic for General-, Visceral -, Vascular- and Transplantation Surgery, University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.
Jing ZhengDepartment of Neurosurgery, Suqian Hospital Affiliated to Xuzhou Medical University, Suqian, China.
Chen LiDepartment of Pharmacy, The First Affiliated Hospital of Guangxi Medical University, Nanning, China.
Wenjie ShiMolecular and Experimental Surgery, Clinic for General-, Visceral -, Vascular- and Transplantation Surgery, University Hospital Magdeburg, Otto-von-Guericke University, Magdeburg, Germany.ORCID 0009-0001-7345-579X
Lifen HuangClinicopathological Diagnosis & Research Center, The Affiliated Hospital of Youjiang Medical University for Nationalities, Baise, China.
Zhengquan YuDepartment of Neurosurgery, The First Affiliated Hospital of Soochow University, Suzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Disulfidptosis, a new form of programmed cell death, plays a role in multiple types of cancer. However, research on disulfidptosis in glioma is lacking. A disulfidptosis-associated risk score was constructed using Cox regression modelling, while LASSO regression was applied for feature selection. To explore the relationship between the risk score and the immune microenvironment, we employed CIBERSORT, ssGSEA and ESTIMATE algorithms. Additionally, wet lab experiments were conducted to validate the functional role of the key disulfidptosis gene RPN1, demonstrating its ability to promote glioma cell proliferation and migration. Disulfidptosis genes were significantly upregulated in gliomas, influencing clinical features and survival. The risk score effectively predicted OS and varied among clinical subgroups. High-risk scores correlated with tumour growth, invasion and immunosuppression. Patients with different risk scores showed distinct immune cell infiltration patterns. Most immune checkpoints and chemokines were positively associated with risk scores. Laboratory findings confirmed that RPN1 significantly promoted glioma cell proliferation and migration. Disulfidptosis-based risk assessment stratifies glioma prognosis and reveals immune microenvironment characteristics, offering insights for personalised treatment strategies.

Indexed as

ApoptosisBrain NeoplasmsGliomaBiomarkers, TumorCell Line, TumorCell MovementCell ProliferationDisulfidptosisFemaleGene Expression Regulation, NeoplasticHumansMalePrognosisRisk AssessmentTumor MicroenvironmentBiomarkers, Tumordisulfidptosisgliomaimmune microenvironmentprognosisrisk score

Identifiers

PMID39993959
PMCPMC11850091

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Registered trials

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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.