Evidence map›Paper›PMID 39397989›Full record

ArticleHeliyon2024

Establish a novel immune-related gene prognostic risk index (IRGPRI) associated with CD8+ cytotoxic T lymphocytes in non-small-cell lung cancer (NSCLC).

Shenjing Cui, Yikun Yang, Shuang Lou, Rong Huang, Jing Wang, Zhongbiao Chen, Jingjing Xie

Abstract read
In one paragraph

Article in Heliyon, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Shenjing CuiDepartment of Clinical Laboratory, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.
Yikun YangDepartment of Thoracic Surgery, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital & Shenzhen Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Shenzhen, China.
Shuang LouDepartment of Clinical Laboratory, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Rong HuangDepartment of Clinical Laboratory, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Jing WangDepartment of Clinical Laboratory, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Zhongbiao ChenDepartment of Clinical Laboratory, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Jingjing XieDepartment of Medical Administration, The University of Hong Kong-Shenzhen Hospital, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The aim of this study is to create an index called IRGPRI (immune-related gene prognostic risk index) that can be utilized for predicting the prognosis and assessing the efficacy of immune checkpoint inhibitors (ICIs) therapy in patients with non-small-cell lung cancer (NSCLC). Methods: Distinguishing gene expression patterns (DEGs) were detected in CD8 Results: A total of 109 genes were identified by intersecting immune-related genes with DEGs obtained from single-cell RNA sequencing data (GSE131907), specifically comparing CTLs to other cell types. From these, we selected 7 prognosis-related genes, namely Conclusions: Our research effectively developed and verified a unique IRGPRI, showcasing its association with immune-related characteristics. As a result, the potential of IRGPRI as a valuable biomarker for predicting prognosis and evaluating the effectiveness of ICIs treatment in cancer is evident.

Indexed as

CTLsImmune checkpoint inhibitorsIRGPRINon-small-cell lung cancerPrognosis

Identifiers

PMID39397989
PMCPMC11466668

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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.