Evidence map›Paper›PMID 38849410›Full record

ArticleScientific reports2024

An immunogenic cell death-related lncRNA signature correlates with prognosis and tumor immune microenvironment in bladder cancer.

Jinhong Luo, Feiye Luo, Qin Li, Qinghong Liu, Jinshan Wang

Abstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Jinhong LuoDepartment of Oncology, East Hospital, Tongji University School of Medicine, No. 1800 Yuntai Road, Shanghai, 200123, China.
Feiye LuoDepartment of Urology, Dongfang People's Hospital, Dongfang, 572699, Hainan Province, China.
Qin LiDepartment of Oncology, East Hospital, Ji'an Hospital, Ji'an, 343000, Jiangxi, China.
Qinghong LiuDepartment of Oncology, East Hospital, Tongji University School of Medicine, No. 1800 Yuntai Road, Shanghai, 200123, China.
Jinshan WangDepartment of Oncology, East Hospital, Tongji University School of Medicine, No. 1800 Yuntai Road, Shanghai, 200123, China. wangjinshan69@163.com.

Funding

Science and Technology Plan of Jiangxi Health Commission SKJP_220202675
6 · The paper itself

Abstract

Immunogenic cell death (ICD) is a newly discovered form of cellular demise that triggers adaptive immune responses mediated by T cells. However, the immunogenic cell death-related lncRNAs (ICDRLs) involved in bladder cancer (BC) development and progression remain to be further elucidated. Molecular profiling data and clinicopathological information for BC patients were obtained from TCGA, and the ICDRGs list was obtained from published literature. For the identification of ICDRLs, Pearson co-expression analysis was performed, and a prognostic signature based on 13 ICDRLs was constructed by univariate assays and LASSO assays. Herein, an ICDRLSig consisting of 13 ICDRLs was constructed. KM curves and ROC curves demonstrated that the constructed signature in the TCGA training, testing, entire and external sets have good predictive performance. Multivariate assays illuminated that the signature is an independent predictor for BC patients' OS, exhibiting greater predictive power for the survival than traditional clinicopathological features. Additionally, patients in the high-ICDRLSig risk subgroup had more abundant immune infiltration, higher immune checkpoint gene expression, lower TMB and poorer response to immunotherapy. We have developed a novel ICDRLSig that can be exploited for survival prediction and provide a reference for further individualized treatment.

Indexed as

Gene Expression Regulation, NeoplasticImmunogenic Cell DeathRNA, Long NoncodingTumor MicroenvironmentUrinary Bladder NeoplasmsAgedBiomarkers, TumorFemaleGene Expression ProfilingHumansKaplan-Meier EstimateMaleMiddle AgedPrognosisROC CurveBiomarkers, TumorRNA, Long NoncodingBladder cancerImmunogenic cell deathlncRNAsNomogramTCGATumor Immune Microenvironment

Identifiers

PMID38849410
PMCPMC11161581

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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.