Evidence map›Paper›PMID 39972939›Full record

ReviewThe journal of gene medicine2025

The Mechanisms, Research Status, and Future Prospects of m6A Modification in Breast Cancer.

Xiu Xue-Mei, Chen Yang, Ju Wen-Ting, Qin Wen-Xing

Abstract readReview
In one paragraph

Review in The journal of gene medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. 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

4 authors.

Xiu Xue-MeiDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.ORCID 0009-0007-1031-0503
Chen YangDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Ju Wen-TingDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.
Qin Wen-XingDepartment of Medical Oncology, Fudan University Shanghai Cancer Center, Shanghai, China.

Funding

Chinese Society of Clinical Oncology Foundation Y-2022HER-2AZMS-0349Chinese Society of Clinical Oncology Foundation Y-2023AZMETMS-0077National Natural Science Foundation of China 81502260Organization Department of Shanghai Municipal Party CommitteeShanghai Science and Technology Commission 23Y11909200Shanghai Science and Technology Commission 24SF1900200Shanghai Xuhui District Science and Technology Committee 23XHYD-6
6 · The paper itself

Abstract

N6-methyladenosine (m6A) modification is a significant methylation alteration frequently observed in eukaryotic RNAs, garnering considerable attention in the field of breast cancer research in recent years. The m6A modification profoundly influences the onset, progression, and prognosis of breast cancer by regulating RNA stability, translation efficiency, and degradation processes. Numerous studies have demonstrated that m6A regulatory factors, including METTL3, METTL14, and ALKBH5, play pivotal roles in breast cancer cells, affecting cell proliferation, metastasis, and drug resistance. Furthermore, the interactions between m6A modification and non-coding RNAs, as well as its role in the tumor microenvironment, have increasingly attracted researchers' interest. Although numerous studies have elucidated the dual roles of m6A in breast cancer, its specific molecular mechanisms remain to be thoroughly investigated. Future research should explore various aspects, including the role of m6A in different subtypes of breast cancer, its involvement in chemotherapy resistance, and its interactions with the tumor microenvironment. This exploration will contribute to advancements in the diagnosis and treatment of breast cancer. The present article aims to systematically summarize the research progress on m6A modification in breast cancer, offering novel insights and strategies for future related research and clinical applications.

Indexed as

AdenosineBreast NeoplasmsDrug Resistance, NeoplasmFemaleGene Expression Regulation, NeoplasticHumansMethylationMethyltransferasesTumor MicroenvironmentAdenosineMethyltransferasesN-methyladenosinebreast cancerdrug resistancem6A modificationregulatory factorsRNA metabolism

Identifiers

PMID39972939
PMCPMC11840220

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.