Evidence map›Paper›PMID 35240991›Full record

ArticleBMC gastroenterology2022

m1A methylation modification patterns and metabolic characteristics in hepatocellular carcinoma.

Chengcheng Tong, Wei Wang, Chiyi He

Open access · goldAbstract read
In one paragraph

Article in BMC gastroenterology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.4field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 17 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

3 authors at 1 institution in 1 country.

Chengcheng Tong *Department of Gastroenterology, Yijishan Hospital of Wannan Medical College, Wuhu, Anhui Province, China.
Wei Wang *Department of Gastroenterology, Yijishan Hospital of Wannan Medical College, Wuhu, Anhui Province, China. wwwy@wnmc.edu.cn.ORCID http://orcid.org/0000-0001-9963-5062
Chiyi HeDepartment of Gastroenterology, Yijishan Hospital of Wannan Medical College, Wuhu, Anhui Province, China. hechiyi11@wnmc.edu.cn.
Wannan Medical College · CN

Funding

Anhui Province Key Research and Development Program Project 201904a07020028Wannan Medical College WK2017F20Yijishan Hospital of Wannan Medical College YR201608
6 · The paper itself

Abstract

backgroundThe dysregulation of RNA methylation has been demonstrated to contribute to tumorigenicity and progression in recent years. However, the alteration of N1-methyladenosine (m1A) methylation and its role in hepatocellular carcinoma (HCC) remain unclear.

methodsWe systematically investigated the modification patterns of 10 m1A regulators in HCC samples and evaluated the metabolic characteristics of each pattern. A scoring system named the m1Ascore was developed using principal component analysis. The clinical value of the m1Ascore in risk stratification and drug screening was further explored.

resultsThree m1A modification patterns with distinct metabolic characteristics were identified, corresponding to the metabolism-high, metabolism-intermediate and metabolism-excluded phenotypes. Patients were divided into high- or low-m1Ascore groups, and a significant survival difference was observed. External validation confirmed the prognostic value of the m1Ascore. A nomogram incorporating the m1Ascore and other clinicopathological factors was constructed and had good performance for predicting survival. Two agents, mitoxantrone and doxorubicin, were determined to be potential therapeutic drugs for the high-risk group.

conclusionThis study provided novel insights into m1A modification and metabolic heterogeneity in cancer, promoted risk stratification in the clinic from the perspective of m1A modification, and further guided individual treatment strategies.

Indexed as

Carcinoma, HepatocellularLiver NeoplasmsRNA Processing, Post-TranscriptionalAdenosineHumansMethylationPrognosis1-methyladenosineAdenosineHepatocellular carcinomam1AMetabolismPrognosis

Identifiers

PMID35240991
PMCPMC8896097
OpenAlexW4214821053

What OpenQuestion holds

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LicenceCC BY
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.