Evidence map›Paper›PMID 38572667›Full record

ReviewClinical and translational medicine2024

RNA methylation-related inhibitors: Biological basis and therapeutic potential for cancer therapy.

Huanxiang Chen, Hongyang Liu, Chenxing Zhang, Nan Xiao, Yang Li, Xiangzhuan Zhao, Ruike Zhang, Huihui Gu, Qiaozhen Kang, Junhu Wan

Open access · goldAbstract readReview
In one paragraph

Review in Clinical and translational medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

8 citing papers in PubMed, 12 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

10 authors at 3 institutions in 1 country.

Huanxiang ChenDepartment of Clinical Laboratory, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Hongyang LiuDepartment of Obstetrics and Gynecology, The Third Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Chenxing ZhangDepartment of Clinical Laboratory, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Nan XiaoDepartment of Clinical Laboratory, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Yang LiDepartment of Clinical Laboratory, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.
Xiangzhuan ZhaoSchool of Life Science, Zhengzhou University, Zhengzhou, China.
Ruike ZhangAcademy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
Huihui GuAcademy of Medical Sciences, Zhengzhou University, Zhengzhou, China.
Qiaozhen KangSchool of Life Science, Zhengzhou University, Zhengzhou, China.
Junhu WanDepartment of Clinical Laboratory, The First Affiliated Hospital of Zhengzhou University, Zhengzhou, China.ORCID 0009-0008-3869-7153
Zhengzhou University · CNFirst Affiliated Hospital of Zhengzhou University · CNThird Affiliated Hospital of Zhengzhou University · CN

Funding

Funding for Scientific Research and Innovation Team of The First Affiliated Hospital of Zhengzhou University QNCXTD2023005Medical Science and Technology Provincial and Ministerial Co-Construction Project of Henan Province SBGJ202102133National Natural Science Foundation of China 82173018National Natural Science Foundation of China 82370113Natural Science Foundation of Henan Province 232300421054Natural Science Foundation of Henan Province 232300421286Young and Middle-Aged Health Science and Technology Innovation Talents Project of Henan Province YXKC2021036Zhengzhou University Education and Teaching Reform Research and Practice Project 2022ZZUJG298
6 · The paper itself

Abstract

RNA methylation is widespread in nature. Abnormal expression of proteins associated with RNA methylation is strongly associated with a number of human diseases including cancer. Increasing evidence suggests that targeting RNA methylation holds promise for cancer treatment. This review specifically describes several common RNA modifications, such as the relatively well-studied N6-methyladenosine, as well as 5-methylcytosine and pseudouridine (Ψ). The regulatory factors involved in these modifications and their roles in RNA are also comprehensively discussed. We summarise the diverse regulatory functions of these modifications across different types of RNAs. Furthermore, we elucidate the structural characteristics of these modifications along with the development of specific inhibitors targeting them. Additionally, recent advancements in small molecule inhibitors targeting RNA modifications are presented to underscore their immense potential and clinical significance in enhancing therapeutic efficacy against cancer. KEY POINTS: In this paper, several important types of RNA modifications and their related regulatory factors are systematically summarised. Several regulatory factors related to RNA modification types were associated with cancer progression, and their relationships with cancer cell migration, invasion, drug resistance and immune environment were summarised. In this paper, the inhibitors targeting different regulators that have been proposed in recent studies are summarised in detail, which is of great significance for the development of RNA modification regulators and cancer treatment in the future.

Indexed as

NeoplasmsRNA Methylation5-MethylcytosineAdenosineCell MovementHumansRNA5-MethylcytosineAdenosineRNAcancerdrug resistanceinhibitorRNA methylation

Identifiers

PMID38572667
PMCPMC10993167
OpenAlexW4393940998

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.