Evidence map›Paper›PMID 31823961›Full record

ArticleMedical science monitor : international medical journal of experimental and clinical research2019

The Prognostic Value of m6A RNA Methylation Regulators in Colon Adenocarcinoma.

Tao Liu, Chenyao Li, Lipeng Jin, Chao Li, Lei Wang

Open access · hybridAbstract read
In one paragraph

Article in Medical science monitor : international medical journal of experimental and clinical research, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
5.9field-weighted citation impact, top 3% 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

43 citing papers in PubMed, 94 citations in OpenAlex.

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  10. m6A-TSHub: Unveiling the Context-specific mGenomics, proteomics & bioinformatics · 2023
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  17. WTAP mediates FOXP3 mRNA stability to promote SMARCE1 expression and augment glycolysis in colon adenocarcinoma.Mammalian genome : official journal of the International Mammalian Genome Society · 2022
    Article
  18. Review
  19. NCancers · 2022
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  20. Role of main RNA modifications in cancer: NSignal transduction and targeted therapy · 2022
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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

5 authors at 2 institutions in 1 country.

Tao LiuDepartment of Colorectal and Anal Surgery, The First Hospital of Jilin University, Changchun, Jilin, China (mainland).
Chenyao LiDepartment of Colorectal and Anal Surgery, The First Hospital of Jilin University, Changchun, Jilin, China (mainland).
Lipeng JinDepartment of Colorectal and Anal Surgery, The First Hospital of Jilin University, Changchun, Jilin, China (mainland).
Chao LiDepartment of Colorectal and Anal Surgery, The First Hospital of Jilin University, Changchun, Jilin, China (mainland).
Lei WangDepartment of Colorectal and Anal Surgery, The First Hospital of Jilin University, Changchun, Jilin, China (mainland).
Jilin University · CNFirst Hospital of Jilin University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND The RNA-seq FPKM data of 331 colorectal adenocarcinoma samples in The Cancer Genome Atlas database with matching clinical data were analyzed in order to reveal the prognostic value of m6A RNA methylation regulators in colon adenocarcinoma. MATERIAL AND METHODS The expression of 13 m6A RNA methylated regulators in samples were analyzed. The samples were classified into Cluster I and II by consistent clustering. The gene distribution was analyzed by principal component analysis. Further functional analysis of selected m6A RNA genes was performed and potential risk characteristics was developed using Lasso Cox regression algorithm. Using minimum criteria, the risk coefficients of YTHDF1 and HNRNPC were detected for Cluster II. Patients were divided into high-risk and low-risk subgroups based on the risk characteristics. The clinical data were analyzed by univariate and multivariate Cox regression analysis. RESULTS Expression of the detected m6A RNA methylated regulators except YTHDC2 in tumors were significantly different from their adjacent mucosa. Among them, only ALKBH5 and METTL4 were downregulated in tumors. The gene distribution between the 2 subgroups were different. The expression of m6A RNA methylation regulators including YTHDF1, HNRNPC, YTHDC2, YTHDC1, ZC3H13, and RBM15 were different between the 2 groups (P<0.05). The prognostic characteristics between the high-risk and low-risk groups were significant different (P<0.05), which had a good predictive significance of prognosis area under the curve (AUC)=0.62). Risk scores were less than 0.05, suggesting risk score was an independent prognostic factor for colon adenocarcinoma. CONCLUSIONS m6A RNA methylation regulators YTHDF1 and HNRNPC can be used as prognostic factors of colon cancer, which has potential value for colon cancer treatment.

Indexed as

AdenocarcinomaAdenosineAdenosine TriphosphatasesAlgorithmsCluster AnalysisColonColonic NeoplasmsDatabases, GeneticGene Expression ProfilingHeterogeneous-Nuclear Ribonucleoprotein Group CHumansMethylationMethyltransferasesMultivariate AnalysisPrognosisRNA6-methyladenine mRNA methyltransferaseAdenosineAdenosine TriphosphatasesHeterogeneous-Nuclear Ribonucleoprotein Group CHNRNPC protein, humanMethyltransferasesRNARNA-Binding ProteinsRNA HelicasestRNA MethyltransferasesYTHDC2 protein, humanYTHDF1 protein, human

Identifiers

PMID31823961
PMCPMC6926093
OpenAlexW2996751782

What OpenQuestion holds

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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.