Evidence map›Paper›PMID 38268051›Full record

ArticleExperimental hematology & oncology2024

METTL1 mediated tRNA m

Pan Zhao, Lin Xia, Dan Chen, Wei Xu, Huanping Guo, Yinying Xu, Bingbing Yan, Xiao Wu, Yuxia Li, Yunfang Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Experimental hematology & oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
8.4field-weighted citation impact, top 2% 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

31 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  11. Article
  12. NSUN2-tRNACellular & molecular biology letters · 2025
    Article
  13. Review
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  15. Article
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  17. Review
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  19. Review
  20. The emerging roles of METTL1-mediated tRNA mFrontiers in immunology · 2025
    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

11 authors at 3 institutions in 1 country.

Pan Zhao *Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.
Lin Xia *Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.
Dan Chen *Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.
Wei Xu *Medical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.
Huanping GuoMedical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.
Yinying XuMedical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.
Bingbing YanMedical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.
Xiao WuMedical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.
Yuxia LiMedical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China.
Yunfang ZhangClinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Shanghai Key Laboratory of Signaling and Disease Research, Frontier Science Center for Stem Cell Research, School of Life Sciences and Technology, Tongji University, Shanghai, 200092, China. zhangyunfang@tongji.edu.cn.
Xi ZhangMedical Center of Hematology, Xinqiao Hospital of Army Medical University, Chongqing, 400037, China. zhangxxi@sina.com.
Xinqiao Hospital · CNArmy Medical University · CNShanghai First Maternity and Infant Hospital · CN

Funding

National Natural Science Foundation of China 82022029National Natural Science Foundation of China 82100182Natural Science Foundation of Sichuan Province 2022NSFSC1416Natural Science Foundation Project of Chongqing, Chongqing Science and Technology Commission cstc2020jcyj-msxmX0732Natural Science Foundation Project of Chongqing, Chongqing Science and Technology Commission cstc2021jcyj-bshX0162
6 · The paper itself

Abstract

backgroundRNA modifications have been proven to play fundamental roles in regulating cellular biology process. Recently, maladjusted N7-methylguanosine (m

methodsMETTL1/WDR4 expression levels were quantified using qRT-PCR, western blot analysis on AML clinical samples, and bioinformatics analysis on publicly available AML datasets. CCK-8 assays and cell count assays were performed to determine cell proliferation. Flow cytometry assays were conducted to assess cell cycle and apoptosis rates. Multiple techniques were used for mechanism studies in vitro assays, such as northern blotting, liquid chromatography-coupled mass spectrometry (LC-MS/MS), tRNA stability analysis, transcriptome sequencing, small non-coding RNA sequencing, quantitative proteomics, and protein synthesis measurements.

resultsMETTL1/WDR4 are significantly elevated in AML patients and associated with poor prognosis. METTL1 knockdown resulted in reduced cell proliferation and increased apoptosis in AML cells. Mechanically, METTL1 knockdown leads to significant decrease of m

conclusionsTaken together, our study demonstrates the important role of METTL1/WDR4 in AML leukaemogenesis, which provides a promising target candidate for AML therapy.

Indexed as

AMLm7GMETTL1/WDR4Translation controltRNA modification

Identifiers

PMID38268051
PMCPMC10807064
OpenAlexW4391174668

What Socratic 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 Socratic graph.