Evidence map›Paper›PMID 32333311›Full record

ArticleDigestive diseases and sciences2021

Identification of METTL3 as an Adverse Prognostic Biomarker in Hepatocellular Carcinoma.

Gao-Min Liu, Hua-Dong Zeng, Cai-Yun Zhang, Ji-Wei Xu

Abstract read
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Article in Digestive diseases and sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

46 citing papers in PubMed, 59 citations in OpenAlex.

  1. Article
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  4. METTL3: a multifunctional regulator in diseases.Molecular and cellular biochemistry · 2025
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  6. Article
  7. Unveiling the dynamics and therapeutic potential of mInternational journal of biological sciences · 2025
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  13. RNA m6A methylation regulators in liver cancer.Cancer cell international · 2024
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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

4 authors at 1 institution in 1 country.

Gao-Min LiuDepartment of Hepatobiliary Surgery, Meizhou People's Hospital, No. 63 Huangtang Road, Meizhou, 514000, China. liugaom88@foxmail.com.ORCID http://orcid.org/0000-0002-8640-2427
Hua-Dong ZengDepartment of Hepatobiliary Surgery, Meizhou People's Hospital, No. 63 Huangtang Road, Meizhou, 514000, China.
Cai-Yun ZhangDepartment of Hepatobiliary Surgery, Meizhou People's Hospital, No. 63 Huangtang Road, Meizhou, 514000, China.
Ji-Wei XuDepartment of Hepatobiliary Surgery, Meizhou People's Hospital, No. 63 Huangtang Road, Meizhou, 514000, China.
Meizhou City People's Hospital · CN

Funding

Guangdong Medical Research Foundation A2017457Peiyu Project of Meizhou People's Hospital PY-C2019004
6 · The paper itself

Abstract

introductionN6-methyladenosine (m6A), the most prominent mRNA modification, plays a critical role in many physiological and pathological processes. However, the roles of m6A RNA modification in hepatocellular carcinoma (HCC) remain largely unknown. MATERIALS AND

methodsWe investigated the mRNA expression and clinical significance of m6A-related genes using data from The Cancer Genome Atlas (TCGA) liver hepatocellular carcinoma cohort. Mutation, copy number variation (CNV), methylation, differential expression, and gene ontology analyses, gene set enrichment analysis and the construction of a competing endogenous RNA (ceRNA) regulatory network were performed to investigate the underlying mechanisms of the aberrant expression of m6A-related genes.

resultsm6A-related genes were frequently dysregulated in cancers but with a cancer-specific pattern. METTL3, YTHDF2, and ZC3H13 were found to be independent prognostic factors of overall survival (OS); however, only METTL3 was found to be an independent prognostic factor of recurrence-free survival (RFS). Joint effects analysis showed the predictive capacity of combining METTL3, YTHDF2, and ZC3H13 for HCC OS. Then the potential mechanisms of METTL3 were further explored due to its prognostic role in both OS and RFS. CNV and DNA methylation, but not somatic mutations, might contribute to the abnormal upregulation of METTL3 in HCC. Significantly altered genes, microRNAs, and lncRNAs were identified, and a ceRNA regulatory network was constructed to explain the upregulation of METTL3 in HCC.

conclusionsOur study identified several m6A-related genes, especially METTL3, that could be potential prognostic biomarkers in HCC.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsMethyltransferasesBiomarkers, TumorDatabases, GeneticDisease ProgressionGene Expression ProfilingGene Expression Regulation, NeoplasticHumansPrognosisUp-RegulationBiomarkers, TumorMethyltransferasesMETTL3 protein, humanceRNAHepatocellular carcinomaMETTL3TCGA

Identifiers

PMID32333311
OpenAlexW3020474159

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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.