Evidence map›Paper›PMID 32600423›Full record

ArticleWorld journal of surgical oncology2020

Prediction and identification of immune genes related to the prognosis of patients with colon adenocarcinoma and its mechanisms.

Sihan Chen, G D Cao, Wu Wei, Lu Yida, He Xiaobo, Yang Lei, Chen Ke, Bo Chen, Mao Ming Xiong

Open access · goldAbstract read
In one paragraph

Article in World journal of surgical oncology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-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

13 citing papers in PubMed, 15 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Sihan ChenDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Aahui, China.
G D CaoDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Aahui, China.
Wu WeiDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Aahui, China.
Lu YidaDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Aahui, China.
He XiaoboDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Aahui, China.
Yang LeiDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Aahui, China.
Chen KeDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Aahui, China.
Bo ChenDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Aahui, China. 23238170@qq.com.
Mao Ming XiongDepartment of General Surgery, The First Affiliated Hospital of Anhui Medical University, Aahui, China. csh940903@stu.ahmu.edu.cn.
First Affiliated Hospital of Anhui Medical University · CNAnhui Medical University · CN

Funding

The Key Research and Development Plan Projects of Anhui Province No.201904a07020045
6 · The paper itself

Abstract

backgroundColon adenocarcinoma (COAD) is a gastrointestinal tumor with a high degree of malignancy. Its deterioration process is closely related to the tumor microenvironment, and transcription factors (TF) play a regulatory role in this process. Currently, there is a lack of exploration between the genes related to the COAD tumor microenvironment and the survival prognosis of patients. Models composed of multiple genes usually predict the survival prognosis of patients more accurately than single genes. We can analyze the multigene models that can predict the prognosis of COAD from the current database.

methodsThe limma package of the R programming language is used for gene differential expression analysis. Kaplan-Meier curve is used to analyze the relationship between the patient risk score model and survival data. The hazard model is used to analyze the relationship between the risk score and the clinical data of COAD patients. The information of immune genes and immune cells is obtained from IMMPORT database and TIMER database. Receiver operating characteristic (ROC) curve is used to judge the stability of the model.

resultsWe found 7 immune genes, which can built a risk score model to predict the survival prognosis of COAD. According to univariate and multivariate analysis, the risk score can be used as an independent predictor. The content of some immune microenvironment cells will also increase as the risk score increases.

conclusionsWe found 7 immune genes, such as SLC10A2 (solute carrier family 10 member 2), CXCL3 (C-X-C motif chemokine ligand 3), IGHV5-51 (immunoglobulin heavy variable 5-51), INHBA (inhibin subunit beta A), STC1 (stanniocalcin 1), UCN (urocortin), and OXTR (oxytocin receptor), can constitute a model for predicting the prognosis of COAD. They may provide potential therapeutic targets for clinical treatment of COAD.

Indexed as

AdenocarcinomaBiomarkers, TumorColonic NeoplasmsComputational BiologyDatabases, GeneticGene Expression ProfilingGene Expression Regulation, NeoplasticHumansPrognosisSurvival RateTumor EscapeTumor MicroenvironmentBiomarkers, TumorBioinformatics analysisColon adenocarcinomaImmune genesPrognosis

Identifiers

PMID32600423
PMCPMC7325073
OpenAlexW3037381138

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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.