Evidence map›Paper›PMID 37516981›Full record

ArticleJournal of cancer research and clinical oncology2023

A novel tetraspanin-related gene signature for predicting prognosis and immune invasion status of lung adenocarcinoma.

Yindong Zhu, Ying Yang, Yuan Liu, Hongyan Qian, Ganlin Qu, Weidong Shi, Jun Liu

Open access · hybridAbstract read
In one paragraph

Article in Journal of cancer research and clinical oncology, 2023. 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
0.2field-weighted citation impact, top 31% 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

0 citing papers in PubMed, 1 citations in OpenAlex.

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 at 3 institutions in 1 country.

Yindong Zhu *Department of Oncology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China.
Ying Yang *Cancer Research Center Nantong, Nantong Tumor Hospital, The Affiliated Tumor Hospital of Nantong University, Nantong University, Nantong, China.
Yuan LiuCancer Research Center Nantong, Nantong Tumor Hospital, The Affiliated Tumor Hospital of Nantong University, Nantong University, Nantong, China.
Hongyan QianCancer Research Center Nantong, Nantong Tumor Hospital, The Affiliated Tumor Hospital of Nantong University, Nantong University, Nantong, China.
Ganlin QuDepartment of Oncology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China.
Weidong ShiDepartment of Thoracic Surgery, The Second People Hospital of Nantong, Nantong, China.
Jun LiuDepartment of Oncology, Affiliated Hospital of Nantong University, Medical School of Nantong University, Nantong, China. liujun11301@hotmail.com.
Nantong University · CNNantong Tumor Hospital · CNAffiliated Hospital of Nantong University · CN

Funding

the Nantong Municipal Health Commission scientific research projects MS2022055the Nantong Municipal Health Commission scientific research projects MSZ2022005the Nantong Municipal Health Commission scientific research projects QA2021028
6 · The paper itself

Abstract

backgroundLung adenocarcinoma (LUAD), the most common subtype of lung cancer, is the primary contributor to cancer-linked fatalities. Dysregulation in the proliferation of cells and death is primarily involved in its development. Recently, tetraspanins, a group of transmembrane proteins, have gained increasing attention for their potential role in the progression of LUAD. Hence, our endeavor involved the development of a novel tetraspanin-based model for the prognostication of lung cancer.

methodsA comprehensive set of bioinformatics tools was utilized to evaluate the expression of tetraspanin-related genes and assess their significance regarding prognosis. Hence, a robust risk signature was established through machine learning. The prognosis-predictive value of the signature was evaluated in terms of clinical application, functional enrichment, and the immune landscape.

resultsThe research first identified differential expression of tetraspanin genes in patients with LUAD via publicly available databases. The resulting data were indicative of the value that nine of them held regarding prognosis. Five distinct elements were utilized in the establishment of a tetraspanin-related model (TSPAN7, TSPAN11, TSPAN14, UPK1B, and UPK1A). Furthermore, as per the median risk scores, the participants were classified into high- and low-risk groups. The model was validated using inner and outer validation sets. Notably, consensus clustering and prognostic score grouping analysis revealed that tetraspanin-related features affect tumor prognosis by modulating tumor immunity. A nomogram based on the tetraspanin gene was constructed with the aim of enhancing the poor prognosis of high-risk groups and facilitating clinical application.

conclusionThrough machine learning algorithms and in vitro experiments, a novel tetraspanin-associated signature was developed and validated for survival prediction in patients with LUAD that reflects tumor immune infiltration. This could potentially provide new and improved measures for diagnosis and therapeutic interventions for LUAD.

Indexed as

Adenocarcinoma of LungBiomarkers, TumorLung NeoplasmsTetraspaninsComputational BiologyFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMaleMiddle AgedNeoplasm InvasivenessPrognosisBiomarkers, TumorTetraspaninsGene signatureLung adenocarcinomaPrognosisTetraspanin-related genesTumor microenvironment

Identifiers

PMID37516981
PMCPMC10590322
OpenAlexW4385386880

What Socratic holds

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LicenceCC BY
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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 Socratic graph.