Evidence map›Paper›PMID 34476213›Full record

ArticleFrontiers in oncology2021

The m6A Methyltransferase METTL14-Mediated N6-Methyladenosine Modification of PTEN mRNA Inhibits Tumor Growth and Metastasis in Stomach Adenocarcinoma.

Qi Yao, Lanzhen He, Xucan Gao, Na Tang, Lifen Lin, Xiaofang Yu, Dong Wang

Open access · goldAbstract read
In one paragraph

Article in Frontiers in oncology, 2021. 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
1.5field-weighted citation impact, top 17% 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, 23 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Review
  6. Article
  7. METTL14‑mediated RNA methylation in digestive system tumors.International journal of molecular medicine · 2023
    Review
  8. Article
  9. Review
  10. METTL14 Regulates PLAGL2/Journal of oncology · 2023
    Article
  11. Article
  12. Role of m6A writers, erasers and readers in cancer.Experimental hematology & oncology · 2022
    Review
  13. Article
  14. Article
  15. Review
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

7 authors at 4 institutions in 1 country.

Qi YaoDepartment of Anorectal Surgery, The Second Clinical Medical College, Jinan University (Shenzhen People's Hospital), Shenzhen, China.
Lanzhen HeDepartment of Colorectal Surgery, The Sixth Affiliated Hospital, Sun Yat-sen University, Guangzhou, China.
Xucan GaoDepartment of Anorectal Surgery, The Second Clinical Medical College, Jinan University (Shenzhen People's Hospital), Shenzhen, China.
Na TangDepartment of Pathology, The Second Clinical Medical College, Jinan University (Shenzhen People's Hospital), Shenzhen, China.
Lifen LinDepartment of Anorectal Surgery, The Second Clinical Medical College, Jinan University (Shenzhen People's Hospital), Shenzhen, China.
Xiaofang YuDepartment of General Surgery, The Second Clinical Medical College, Jinan University (Shenzhen People's Hospital), Shenzhen, China.
Dong WangDepartment of Anorectal Surgery, The Second Clinical Medical College, Jinan University (Shenzhen People's Hospital), Shenzhen, China.
Southern University of Science and Technology · CNShenzhen Second People's Hospital · CNJinan University · CNSun Yat-sen University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStomach adenocarcinoma (STAD) is a common reason for tumor-related fatalities globally, as it results in distant metastasis. Methyltransferase-like 14 (METTL14), a notable RNA N6-adenosine methyltransferase (m6A), plays a significant role in the growth of tumor through controlling the RNA working. This study aims to highlight METTL14 in STAD's biological function and molecular mechanism.

methodsBioinformatics and immunohistochemical (IHC) assays have been utilized for the detection of METTL14 expression in the STAD. METTL14's biological function has been shown while making use of HGC-27 and AGS cells

resultsMETTL14 expression was substantially downregulated in STAD reflecting contribution to major tumors, progressed TNM stage as well as poor overall survival (OS) in STAD. Moreover, METTL14's inhibition of STAD cells proliferation, migration and invasion has been verified

conclusionsMETTL14 inhibits tumor growth and metastasis of STAD

Indexed as

m6A modificationmetastasisMETTL14PtenSTADtumor growth

Identifiers

PMID34476213
PMCPMC8406853
OpenAlexW3193259668

What OpenQuestion holds

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LicenceCC BY
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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.