Evidence map›Paper›PMID 33910576›Full record

ArticleBMC medical genomics2021

Gene expression and DNA methylation analyses suggest that two immune related genes are prognostic factors of colorectal cancer.

Xiao-Liang Xing, Zhi-Yong Yao, Chaoqun Xing, Zhi Huang, Jing Peng, Yuan-Wu Liu

Open access · goldAbstract read
In one paragraph

Article in BMC medical genomics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
0.9field-weighted citation impact, top 23% 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

6 citing papers in PubMed, 11 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

6 authors at 3 institutions in 1 country.

Xiao-Liang XingXiangya Hospital, Central South University, Changsha, 410078, Hunan, People's Republic of China.
Zhi-Yong YaoHunan University of Medicine, Huaihua, 418000, Hunan, People's Republic of China.
Chaoqun XingHunan University of Medicine, Huaihua, 418000, Hunan, People's Republic of China.
Zhi HuangHunan University of Medicine, Huaihua, 418000, Hunan, People's Republic of China.
Jing PengXiangya Hospital, Central South University, Changsha, 410078, Hunan, People's Republic of China. pengjing4346@163.com.
Yuan-Wu LiuBeijing Advanced Innovation Center for Food Nutrition and Human Health, China Agricultural University, Beijing, 100193, People's Republic of China. yuanwu_liu@126.com.
Hunan University · CNCentral South University · CNChina Agricultural University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundColorectal cancer (CRC) is the second most prevalent cancer, as it accounts for approximately 10% of all annually diagnosed cancers. Studies have indicated that DNA methylation is involved in cancer genesis. The purpose of this study was to investigate the relationships among DNA methylation, gene expression and the tumor-immune microenvironment of CRC, and finally, to identify potential key genes related to immune cell infiltration in CRC.

methodsIn the present study, we used the ChAMP and DESeq2 packages, correlation analyses, and Cox regression analyses to identify immune-related differentially expressed genes (IR-DEGs) that were correlated with aberrant methylation and to construct a risk assessment model.

resultsFinally, we found that HSPA1A expression and CCRL2 expression were positively and negatively associated with the risk score of CRC, respectively. Patients in the high-risk group were more positively correlated with some types of tumor-infiltrating immune cells, whereas they were negatively correlated with other tumor-infiltrating immune cells. After the patients were regrouped according to the median risk score, we could more effectively distinguish them based on survival outcome, clinicopathological characteristics, specific tumor-immune infiltration status and highly expressed immune-related biomarkers.

conclusionThis study suggested that the risk assessment model constructed by pairing immune-related differentially expressed genes correlated with aberrant DNA methylation could predict the outcome of CRC patients and might help to identify those patients who could benefit from antitumor immunotherapy.

Indexed as

Biomarkers, TumorColorectal NeoplasmsDNA MethylationGene Expression Regulation, NeoplasticFemaleGene Expression ProfilingHSP70 Heat-Shock ProteinsHumansMaleMiddle AgedPrognosisTumor MicroenvironmentBiomarkers, TumorHSP70 Heat-Shock ProteinsHSPA1A protein, humanColorectal cancerImmune-related differentially expressed genesMethylationRisk modelTumor-immune microenvironment

Identifiers

PMID33910576
PMCPMC8080337
OpenAlexW3158530480

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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 OpenQuestion graph.