Evidence map›Paper›PMID 36810281›Full record

ReviewExperimental hematology & oncology2023

Emerging roles of m6A RNA modification in cancer therapeutic resistance.

Wei-Wei Liu, Zhong-Yuan Zhang, Fei Wang, Hao Wang

Open access · goldAbstract readReview
In one paragraph

Review in Experimental hematology & oncology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
7.8field-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

24 citing papers in PubMed, 47 citations in OpenAlex.

  1. Review
  2. NNature reviews. Cancer · 2026
    Review
  3. Review
  4. Article
  5. Unraveling the dual role of METTL3-mediated mCancer biology & therapy · 2025
    Review
  6. Review
  7. Review
  8. Review
  9. Article
  10. Chemically modified non-coding RNAs in cancer.Expert reviews in molecular medicine · 2025
    Review
  11. Article
  12. Article
  13. YTHDF1 and YTHDC1 mJournal of virology · 2025
    Article
  14. Review
  15. NClinical and translational medicine · 2024
    Article
  16. Review
  17. Review
  18. Review
  19. METTL1 mediated tRNA mExperimental hematology & oncology · 2024
    Article
  20. Article
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

4 authors at 2 institutions in 1 country.

Wei-Wei Liu *Department of Laboratory Medicine, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Zhong-Yuan Zhang *Department of Radiology, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China.
Fei WangNeurosurgical Department, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China. neurosurgeonwf1@ustc.edu.cn.
Hao WangDepartment of Laboratory Medicine, The First Affiliated Hospital of USTC, Division of Life Sciences and Medicine, University of Science and Technology of China, Hefei, China. demo@ustc.edu.cn.
University of Science and Technology of China · CNShandong University · CN

Funding

Natural Science Foundation of Anhui Province 2008085MH241Youth Innovation Project of University of Science and Technology of China WK9110000203
6 · The paper itself

Abstract

Marvelous advancements have been made in cancer therapies to improve clinical outcomes over the years. However, therapeutic resistance has always been a major difficulty in cancer therapy, with extremely complicated mechanisms remain elusive. N6-methyladenosine (m6A) RNA modification, a hotspot in epigenetics, has gained growing attention as a potential determinant of therapeutic resistance. As the most prevalent RNA modification, m6A is involved in every links of RNA metabolism, including RNA splicing, nuclear export, translation and stability. Three kinds of regulators, "writer" (methyltransferase), "eraser" (demethylase) and "reader" (m6A binding proteins), together orchestrate the dynamic and reversible process of m6A modification. Herein, we primarily reviewed the regulatory mechanisms of m6A in therapeutic resistance, including chemotherapy, targeted therapy, radiotherapy and immunotherapy. Then we discussed the clinical potential of m6A modification to overcome resistance and optimize cancer therapy. Additionally, we proposed existing problems in current research and prospects for future research.

Indexed as

Cancer therapyChemoresistanceImmunotherapym6A

Identifiers

PMID36810281
PMCPMC9942381
OpenAlexW4321452350

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.