Evidence map›Paper›PMID 37197482›Full record

ArticleJournal of thoracic disease2023

A new prognostic model for

Qiao Li, Xiao-Li Liu, Ni Jiang, Qian-Yun Li, Yong-Xiang Song, Xi-Xian Ke, Hao Han, Qian Luo, Qiang Guo, Xiang-Yu Luo and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of thoracic disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 2 pooled it
3.1field-weighted citation impact, top 8% of its field
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

12 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Pooled it
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  12. Atypical RhoUV GTPases in development and disease.Biochemical Society transactions · 2024
    Review
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

11 authors at 5 institutions in 1 country.

Qiao Li *Department of Thoracic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Xiao-Li Liu *Department of Ultrasound, The People's Hospital of Jianyang City, Jianyang, China.
Ni Jiang *Department of Obstetrics and Gynecology, Women and Children's Hospital of Chongqing Medical University, Chongqing, China.
Qian-Yun LiThe Fourth Affiliated Hospital, Zhejiang University School of Medicine, Yiwu, China.
Yong-Xiang SongDepartment of Thoracic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Xi-Xian KeDepartment of Thoracic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Hao HanDepartment of Thoracic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Qian LuoDepartment of Thoracic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Qiang GuoDepartment of Thoracic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Xiang-Yu LuoDepartment of Cardiothoracic Surgery, Taihe Hospital, Hubei University of Medicine, Shiyan, China.
Cheng ChenDepartment of Thoracic Surgery, Affiliated Hospital of Zunyi Medical University, Zunyi, China.
Zunyi Medical University · CNChongqing Medical University · CNFuyang City People's Hospital · CNTaihe Hospital · CNZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lymph node metastasis is one of the important factors affecting the prognosis of lung adenocarcinoma (LUAD) patients. The key molecules in lymph node metastasis have not yet been fully revealed. Therefore, we aimed to construct a prognostic model based on lymph node metastasis-related genes to evaluate the prognosis of LUAD patients. Methods: The differentially expressed genes (DEGs) in the process of LUAD metastasis were identified in The Cancer Genome Atlas (TCGA) database, and the biological roles of the DEGs were depicted using Gene Ontology (GO), Kyoto Encyclopedia of Genes and Genomes (KEGG), and a protein-protein interaction (PPI) network. Survival analysis and Cox regression analysis were used to identify the genes related to the prognosis of patients with LUAD, and a nomogram and a prognostic model were constructed. The potential prognostic value, immune escape, and regulatory mechanisms of the prognostic model in LUAD progression were explored through survival analysis and gene set enrichment analysis (GSEA). Results: A total of 75 genes were upregulated, and 138 genes were downregulated in tissues of lymph node metastasis. The expression levels of Conclusions: Lymph node metastasis-related genes

Indexed as

ABCC2CYP4B1lung adenocarcinoma (LUAD)lymph node metastasisRHOV

Identifiers

PMID37197482
PMCPMC10183535
OpenAlexW4364322325

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.