Evidence map›Paper›PMID 33863999›Full record

ArticleOncogene2021

MEF2A transcriptionally upregulates the expression of ZEB2 and CTNNB1 in colorectal cancer to promote tumor progression.

Qing Xiao, Yaqi Gan, Yimin Li, Lili Fan, Jiaqi Liu, Pengyan Lu, Jiaxin Liu, Aoao Chen, Guang Shu, Gang Yin

Erratum issuedOpen access · hybridAbstract read
In one paragraph

Article in Oncogene, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
3.7field-weighted citation impact, top 5% 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, 58 citations in OpenAlex.

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  15. Single nucleotide polymorphisms ofAnimal biotechnology · 2024
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors at 1 institution in 1 country.

Qing XiaoDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Yaqi GanDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Yimin LiDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Lili FanDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Jiaqi LiuDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Pengyan LuDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Jiaxin LiuDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China.
Aoao ChenDepartment of Immunology, School of Basic Medical Sciences, Central South University, Changsha, China.
Guang ShuDepartment of Histology and Embryology, School of Basic Medical Sciences, Central South University, Changsha, China.
Gang YinDepartment of Pathology, Xiangya Hospital, School of Basic Medical Sciences, Central South University, Changsha, China. gangyin@csu.edu.cn.ORCID http://orcid.org/0000-0003-3753-0753
Central South University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Colorectal cancer (CRC) is one of the leading cancers worldwide, accounting for high morbidity and mortality. The mechanisms governing tumor growth and metastasis in CRC require detailed investigation. The results of the present study indicated that the transcription factor (TF) myocyte enhancer factor 2A (MEF2A) plays a dual role in promoting proliferation and metastasis of CRC by inducing the epithelial-mesenchymal transition (EMT) and activation of WNT/β-catenin signaling. Aberrant expression of MEF2A in CRC clinical specimens was significantly associated with poor prognosis and metastasis. Functionally, MEF2A directly binds to the promoter region to initiate the transcription of ZEB2 and CTNNB1. Simultaneous activation of the expression of EMT-related TFs and Wnt/β-catenin signaling by MEF2A overexpression induced the EMT and increased the frequency of tumor formation and metastasis. The present study identified a new critical oncogene involved in the growth and metastasis of CRC, providing a potential novel therapeutic target for CRC intervention.

Indexed as

Animalsbeta CateninCell Line, TumorCell ProliferationColorectal NeoplasmsDisease ProgressionEpithelial-Mesenchymal TransitionHeterograftsHumansMaleMEF2 Transcription FactorsMiceMice, Inbred BALB CMice, NudeNeoplasm GradingSurvival Ratebeta CateninCTNNB1 protein, humanMEF2A protein, humanMEF2 Transcription FactorsZEB2 protein, humanZinc Finger E-box Binding Homeobox 2

Identifiers

PMID33863999
PMCPMC8116210
OpenAlexW3156010630

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.