Evidence map›Paper›PMID 35628623›Full record

ReviewInternational journal of molecular sciences2022

Recent Advances of m6A Demethylases Inhibitors and Their Biological Functions in Human Diseases.

Yazhen You, Yundong Fu, Mingjie Huang, Dandan Shen, Bing Zhao, Hongmin Liu, Yichao Zheng, Lihua Huang

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 66 citations in OpenAlex.

  1. mExperimental and therapeutic medicine · 2026
    Review
  2. Review
  3. NBiomolecules · 2026
    Review
  4. Review
  5. mFrontiers in immunology · 2026
    Review
  6. Review
  7. Article
  8. Role of the mInternational journal of molecular medicine · 2025
    Review
  9. Review
  10. Review
  11. Review
  12. ALKBH5 in development: decoding the multifaceted roles of mFrontiers in molecular biosciences · 2025
    Review
  13. Article
  14. Review
  15. Review
  16. Review
  17. Article
  18. Review
  19. NMolecular biotechnology · 2024
    Article
  20. 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

8 authors at 1 institution in 1 country.

Yazhen YouGreen Catalysis Center, College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
Yundong FuGreen Catalysis Center, College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
Mingjie HuangGreen Catalysis Center, College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
Dandan ShenSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Bing ZhaoSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Hongmin LiuSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Yichao ZhengSchool of Pharmaceutical Sciences, Zhengzhou University, Zhengzhou 450001, China.
Lihua HuangGreen Catalysis Center, College of Chemistry, Zhengzhou University, Zhengzhou 450001, China.
Zhengzhou University · CN

Funding

National Key Research Program 2018YFE0195100, 2016YFA0501800, 2017YFD0501401National Natural Science Foundation of China 81602961, 81430085, 81773562, 81903447Science and Technology Innovation Talents of Henan Provincial Education Department 19IRTSTHN001
6 · The paper itself

Abstract

N6-methyladenosine (m6A) is a post-transcriptional RNA modification and one of the most abundant types of RNA chemical modifications. m6A functions as a molecular switch and is involved in a range of biomedical aspects, including cardiovascular diseases, the central nervous system, and cancers. Conceptually, m6A methylation can be dynamically and reversibly modulated by RNA methylation regulatory proteins, resulting in diverse fates of mRNAs. This review focuses on m6A demethylases fat-mass- and obesity-associated protein (FTO) and alkB homolog 5 (ALKBH5), which especially erase m6A modification from target mRNAs. Recent advances have highlighted that FTO and ALKBH5 play an oncogenic role in various cancers, such as acute myeloid leukemias (AML), glioblastoma, and breast cancer. Moreover, studies in vitro and in

Indexed as

AdenosineLeukemia, Myeloid, AcuteAlpha-Ketoglutarate-Dependent Dioxygenase FTOAnimalsHumansMethylationMiceRNARNA, MessengerAdenosineAlpha-Ketoglutarate-Dependent Dioxygenase FTOFTO protein, humanRNARNA, MessengerAKBH5FTOhuman diseasesinhibitorsm6A demethylases

Identifiers

PMID35628623
PMCPMC9144293
OpenAlexW4281250482

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.