Evidence map›Paper›PMID 36939925›Full record

ArticleJournal of cancer research and clinical oncology2023

Machine learning-based immune prognostic model and ceRNA network construction for lung adenocarcinoma.

Xiaoqian He, Ying Su, Pei Liu, Cheng Chen, Chen Chen, Haoqin Guan, Xiaoyi Lv, Wenjia Guo

Open access · greenAbstract 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. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.0field-weighted citation impact, top 22% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Cadherin 17 and digestive cancers: from diagnostic to therapeutic opportunities.Journal of experimental & clinical cancer research : CR · 2026
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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

8 authors at 2 institutions in 1 country.

Xiaoqian HeCollege of Information Science and Engineering, Xinjiang University, Urumqi, 830046, China.
Ying SuCollege of Information Science and Engineering, Xinjiang University, Urumqi, 830046, China.
Pei LiuCollege of Information Science and Engineering, Xinjiang University, Urumqi, 830046, China.
Cheng ChenCollege of Software, Xinjiang University, Urumqi, 830046, China. chenchengoptics@gmail.com.
Chen ChenCollege of Information Science and Engineering, Xinjiang University, Urumqi, 830046, China.
Haoqin GuanCollege of Information Science and Engineering, Xinjiang University, Urumqi, 830046, China.
Xiaoyi LvCollege of Software, Xinjiang University, Urumqi, 830046, China. xjuwawj01@163.com.
Wenjia GuoAffiliated Tumor Hospital of Xinjiang Medical University, Urumqi, 830011, China. wenjiaguo@xjmu.edu.cn.
Xinjiang University · CNTumor Hospital of Xinjiang Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeLung adenocarcinoma (LUAD) is a malignant tumor with a high lethality rate. Immunotherapy has become a breakthrough in cancer treatment and improves patient survival and prognosis. Therefore, it is necessary to find new immune-related markers. However, the current research on immune-related markers in LUAD is not sufficient. Therefore, there is a need to find new immune-related biomarkers to help treat LUAD patients.

methodsIn this study, a bioinformatics approach combined with a machine learning approach screened reliable immune-related markers to construct a prognostic model to predict the overall survival (OS) of LUAD patients, thus promoting the clinical application of immunotherapy in LUAD. The experimental data were obtained from The Cancer Genome Atlas (TCGA) database, including 535 LUAD and 59 healthy control samples. Firstly, the Hub gene was screened using a bioinformatics approach combined with the Support Vector Machine Recursive Feature Elimination algorithm; then, a multifactorial Cox regression analysis by constructing an immune prognostic model for LUAD and a nomogram to predict the OS rate of LUAD patients. Finally, the regulatory mechanism of Hub genes in LUAD was analyzed by ceRNA.

resultsFive genes, ADM2, CDH17, DKK1, PTX3, and AC145343.1, were screened as potential immune-related genes in LUAD. Among them, ADM2 and AC145343.1 had a good prognosis in LUAD patients (HR < 1) and were novel markers. The remaining three genes screened were associated with poor prognosis in LUAD patients (HR > 1). In addition, the experimental results showed that patients in the low-risk group had better OS rates than those in the high-risk group (P < 0.001).

conclusionIn this paper, we propose an immune prognostic model to predict OS rate in LUAD patients and show the correlation between five immune genes and the level of immune-related cell infiltration. It provides new markers and additional ideas for immunotherapy in patients with LUAD.

Indexed as

Adenocarcinoma of LungLung NeoplasmsPeptide HormonesHumansMachine LearningNomogramsPrognosisADM2 protein, humanPeptide HormonesceRNAImmune prognostic modelLung adenocarcinomaSVM-RFEWGCNA

Identifiers

PMID36939925
PMCPMC11797472
OpenAlexW4327896529

What OpenQuestion holds

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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.