Evidence map›Paper›PMID 41814329›Full record

ArticleBiology direct2026

miR-196b inhibits tumor proliferation and metastasis by targeting GATA6 in endometrial cancer.

Zhenzhen Guo, Yangyou Liao, Yijing Yang, Xinrui Li, Ning Wang, Yuhong Shang, Hongxiu Liu, Ying Kong, Linlin Sui

Abstract read
In one paragraph

Article in Biology direct, 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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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Zhenzhen Guo *Core Laboratory of Glycobiology and Glycoengineering, College of Basic Medical Sciences, Dalian Medical University, Dalian, Liaoning, 116044, China.
Yangyou Liao *Core Laboratory of Glycobiology and Glycoengineering, College of Basic Medical Sciences, Dalian Medical University, Dalian, Liaoning, 116044, China.
Yijing YangCore Laboratory of Glycobiology and Glycoengineering, College of Basic Medical Sciences, Dalian Medical University, Dalian, Liaoning, 116044, China.
Xinrui LiCore Laboratory of Glycobiology and Glycoengineering, College of Basic Medical Sciences, Dalian Medical University, Dalian, Liaoning, 116044, China.
Ning WangCore Laboratory of Glycobiology and Glycoengineering, College of Basic Medical Sciences, Dalian Medical University, Dalian, Liaoning, 116044, China.
Yuhong ShangDepartment of Gynecology, The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, 116011, China.
Hongxiu LiuDepartment of Gynecology, The Second Hospital of Dalian Medical University, Dalian, Liaoning, 116023, China. huakaifang2006@126.com.
Ying KongCore Laboratory of Glycobiology and Glycoengineering, College of Basic Medical Sciences, Dalian Medical University, Dalian, Liaoning, 116044, China. yingkong@dmu.edu.cn.
Linlin SuiCore Laboratory of Glycobiology and Glycoengineering, College of Basic Medical Sciences, Dalian Medical University, Dalian, Liaoning, 116044, China. suill06@dmu.edu.cn.

Funding

Fund of the Department of Science and Technology of Liaoning Province 2024-MSLH-117Liaoning Provincial Department of Education Project JYTMS20230570
6 · The paper itself

Abstract

backgroundEndometrial cancer (EC) is a common gynecological malignancy with increasing incidence, yet its precise pathogenesis remains unclear. MicroRNAs (miRNAs) have been widely implicated in tumorigenesis. Although studies suggest that miR-196b is closely associated with the progression of various malignancies, its specific biological functions and mechanisms in EC remain to be elucidated.

resultsIn this study, analysis of tissue and serum samples from EC patients revealed that miR-196b is downregulated in EC, whereas GATA6 is upregulated, with a notable negative correlation between their expression levels. In Ishikawa and HEC-1 A EC cell lines, functional assays including CCK-8, colony formation, wound healing, and Transwell experiments revealed that downregulation of miR-196b significantly enhanced cell proliferation, migration, and invasion. A nude mouse xenograft model further confirmed that high miR-196b expression weakened the tumorigenic ability of EC cells. Mechanistically, dual-luciferase reporter assays identified GATA6 as a direct target of miR-196b. Downregulation of miR-196b facilitated the proliferation, metastasis, and epithelial-mesenchymal transition (EMT) of EC cells by up-regulating GATA6. The miR-196b/GATA6 axis is involved in regulating the activity of the AKT/ERK signaling pathway. Furthermore, through a series of bioinformatics analyses, we found that miR-196b and GATA6 have potential as diagnostic and prognostic markers for EC.

conclusionsThis study elucidates the molecular mechanism by which miR-196b suppresses EC progression by targeting GATA6. These findings provide novel insights into the pathogenesis of EC and highlight the potential of miR-196b/GATA6 as a diagnostic and prognostic biomarker.

Indexed as

Cell ProliferationEndometrial NeoplasmsGATA6 Transcription FactorMicroRNAsAnimalsCell Line, TumorCell MovementEpithelial-Mesenchymal TransitionFemaleGene Expression Regulation, NeoplasticHumansMiceMice, NudeNeoplasm MetastasisGATA6 protein, humanGATA6 Transcription FactorMicroRNAsMIRN196 microRNA, humanEndometrial cancerGATA6MetastasismiR-196bTumor proliferation

Identifiers

PMID41814329
PMCPMC13088493

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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.