Evidence map›Paper›PMID 32793281›Full record

ArticleFrontiers in genetics2020

Prognostic Implications of Immune-Related Genes' (IRGs) Signature Models in Cervical Cancer and Endometrial Cancer.

Hao Ding, Guan-Lan Fan, Yue-Xiong Yi, Wei Zhang, Xiao-Xing Xiong, Omer Kamal Mahgoub

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In one paragraph

Article in Frontiers in genetics, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers.

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0cells of the map it votes in
26citing 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

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3 · Its place in the literature

Who cites it

26 citing papers in PubMed.

  1. Article
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  4. SDC1 is a critical transmembrane proteoglycan in breast cancer.World journal of surgical oncology · 2025
    Review
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  6. Machine learning endometrial cancer risk prediction model: integrating guidelines of European Society for Medical Oncology with the tumor immune framework.International journal of gynecological cancer : official journal of the International Gynecological Cancer Society · 2023
    Article
  7. Article
  8. High RIG-I and EFTUD2 expression predicts poor survival in endometrial cancer.Journal of cancer research and clinical oncology · 2023
    Article
  9. Article
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  12. Identification of 8-gene risk prediction signature associated withJournal of gastrointestinal oncology · 2022
    Article
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  15. Review
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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

6 authors.

Hao DingDepartment of Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Guan-Lan FanDepartment of Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Yue-Xiong YiDepartment of Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Wei ZhangDepartment of Gynecology, Zhongnan Hospital of Wuhan University, Wuhan, China.
Xiao-Xing XiongCentral Laboratory, Renmin Hospital of Wuhan University, Wuhan, China.
Omer Kamal MahgoubCentral Laboratory, Renmin Hospital of Wuhan University, Wuhan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cervical cancer and endometrial cancer remain serious threats to women's health. Even though some patients can be treated with surgery plus chemoradiotherapy as a conventional option, the overall efficacy is deemed unsatisfactory. As such, the development for new treatment approaches is truly necessary. In recent years, immunotherapy has been widely used in clinical practice and it is an area of great interest that researchers are keeping attention on. However, a thorough immune-related genes (IRGs) study for cervical cancer and endometrial cancer is still lacking. We therefore aim to make a comprehensive evaluation of IRGs through bioinformatics and large databases, and also investigate the relationship between the two types of cancer. We reviewed the transcriptome RNAs of IRGs and clinical data based on the TCGA database. Survival-associated IRGs in cervical/endometrial cancer were identified using univariable and multivariable Cox proportional-hazard regression analysis for developing an IRG signature model to evaluate the risk of patients. In the end, this model was validated based on the enrichment analyses through GO, KEGG, and GSEA pathways, Kaplan-Meier survival curve, ROC curves, and immune cell infiltration. Our results showed that out of 25/23 survival-associated IRGs for cervical/endometrial cancer, 13/12 warranted further examination by multivariate Cox proportional-hazard regression analysis and were selected to develop an IRGs signature model. As a result, enrichment analyses for high-risk groups indicated main enriched pathways were associated with tumor development and progression, and statistical differences were found between high-risk and low-risk groups as shown by Kaplan-Meier survival curve. This model could be used as an independent measure for risk assessment and was considered relevant to immune cell infiltration, but it had nothing to do with clinicopathological characteristics. In summary, based on comprehensive analysis, we obtained the IRGs signature model in cervical cancer (

Indexed as

cervical cancerendometrial cancerimmune-related genesprognostic modelTCGA

Identifiers

PMID32793281
PMCPMC7385326

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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.