Evidence map›Paper›PMID 36429032›Full record

ArticleCells2022

RNA N6-Methyladenosine (m6A) Methyltransferase-like 3 Facilitates Tumorigenesis and Cisplatin Resistance of Arecoline-Exposed Oral Carcinoma.

Chuang Wang, Chamila Kadigamuwa, Songlv Wu, Yijun Gao, Wuya Chen, Yangcong Gu, Shengli Wang, Xia Li

Open access · goldAbstract read
In one paragraph

Article in Cells, 2022. 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
1.2field-weighted citation impact, top 22% 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, 14 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

8 authors at 3 institutions in 2 countries.

Chuang WangDepartment of Oral Medicine, Foshan Stomatological Hospital, Medical College of Foshan University, Foshan 528000, China.
Chamila KadigamuwaDepartment of Chemistry, University of Kelaniya, Kelaniya 11600, Sri Lanka.ORCID 0000-0001-8210-9533
Songlv WuDepartment of Oral Medicine, Foshan Stomatological Hospital, Medical College of Foshan University, Foshan 528000, China.
Yijun GaoDepartment of Stomatology, The Second Xiangya Hospital, Central South University, Changsha 410008, China.ORCID 0000-0002-2588-5891
Wuya ChenDepartment of Oral Medicine, Foshan Stomatological Hospital, Medical College of Foshan University, Foshan 528000, China.
Yangcong GuDepartment of Oral Maxillofacial Surgery, Foshan Stomatological Hospital, Medical College of Foshan University, Foshan 528000, China.
Shengli WangDepartment of Oral Medicine, Foshan Stomatological Hospital, Medical College of Foshan University, Foshan 528000, China.
Xia LiDepartment of Oral Medicine, Foshan Stomatological Hospital, Medical College of Foshan University, Foshan 528000, China.
Foshan University · CNCentral South University · CNUniversity of Kelaniya · LK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundArecoline is known as the main active carcinogen found in areca nut extract that drives the pathological progression of oral squamous cell carcinoma (OSCC). Studies have revealed that dysregulation of RNA N6-methyladenosine (m6A) methyltransferase components is intimately linked to cancer initiation and progression, including oral cancer.

methodsThe arecoline-induced dysregulated methyltransferase-like 3 (METTL3) gene was identified using RNA-seq transcriptome assay. Using in vitro and in vivo models, the biological roles of METTL3 in arecoline-transformed oral cancer were examined.

resultsWe found that METTL3 was markedly elevated in arecoline-exposed OSCC cell lines and OSCC tissues of areca nut chewers. We identified that hypoxia-inducible factor 1-alpha (HIF-1α) stimulated METTL3 expression at the transcriptional level and further proved that METTL3-MYC-HIF-1α formed a positive autoregulation loop in arecoline-transformed OSCC cells. Subsequently, we manifested that METTL3 depletion profoundly reduced cell proliferation, cell migration, oncogenicity, and cisplatin resistance of arecoline-exposed OSCC cells.

conclusionsDeveloping novel strategies to target METTL3 may be a potential way to treat OSCC patients, particularly those with areca nut chewing history and receiving cisplatin treatment.

Indexed as

Carcinoma, Squamous CellMouth NeoplasmsAdenosineArecolineCarcinogenesisCell Transformation, NeoplasticCisplatinHumansMethyltransferasesRNAAdenosineArecolineCisplatinMethyltransferasesMETTL3 protein, humanRNAarecolinecisplatin resistancemethyltransferase-like 3oral squamous cell carcinomatumorigenesis

Identifiers

PMID36429032
PMCPMC9688745
OpenAlexW4309743906

What OpenQuestion holds

Textmetadata
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.