Evidence map›Paper›PMID 40611422›Full record

ReviewCurrent topics in medicinal chemistry2026

MEF2C: A Novel Transcription Factor Implicated in Human Malignant Tumors.

Yining Pan, Jiayi Li, Haoran Liu, Jiayi Ma, Dongshuo Wang, Xiaolan Li, Chengfu Yuan

Abstract readReview
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In one paragraph

Review in Current topics in medicinal chemistry, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Yining PanHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, China.
Jiayi LiHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, China.
Haoran LiuHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, China.
Jiayi MaHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, China.
Dongshuo WangHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, China.
Xiaolan LiThe Second People's Hospital of China Three Gorges University, China.
Chengfu YuanHubei Key Laboratory of Tumor Microenvironment and Immunotherapy, China Three Gorges University, China.ORCID 0000-0002-1894-0960

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMyocyte enhancer factor 2C (MEF2C) is a pivotal transcription factor that is responsible for maintaining myocyte differentiation. MEF2C is multifunctional, participating in diverse biological processes, including cardiac morphogenesis, angiogenesis, neurogenesis, and cortical development. Emerging evidence has identified MEF2C as a novel oncogene with dual regulatory functions in tumorigenesis. However, the mechanisms by which MEF2C regulates the progression of various malignant tumors are unknown. Therefore, it is crucial to further investigate the multiple signaling pathways under different expression levels of MEF2C. In this review, the expression level of MEF2C in various malignant tumors and its specific pathways are described.

methodsThis review systematically summarizes and critically analyzes the current studies on MEF2C's biological function in malignant tumors by comprehensively searching them in PubMed databases.

resultsMEF2C demonstrates aberrant expression patterns across multiple tumor types, spanning both solid tumors (e.g., glioma, breast cancer, hepatocellular carcinoma) and hematological malignancies (e.g., leukemia). MEF2C orchestrates multiple oncogenic processes, including tumor cell proliferation, migration, and invasion, while also modulating cancer drug resistance and systemic manifestations, like cachexia and apoptosis resistance.

conclusionGiven its multifaceted roles in tumor initiation, progression, and clinical aspects, MEF2C has the potential to serve as both a diagnostic biomarker and a therapeutic target for various malignancies.

Indexed as

MEF2 Transcription FactorsNeoplasmsCell ProliferationHumansMEF2C protein, humanMEF2 Transcription FactorsMalignant tumorsMechanismMEF2CPrognosisTreatmentTumorigenesis

Identifiers

PMID40611422

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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.