Evidence map›Paper›PMID 39823268›Full record

ArticleJournal of cellular and molecular medicine2025

miR-143-3p/TET1 Axis Regulates GPC1 Through DNA Methylation and Impairs the Malignant Biological Behaviour of HCC via the Hippo Signalling Pathway.

Yan Liu, Di Du, Xue Gu, Qing He, Bin Xiong

Abstract read
In one paragraph

Article in Journal of cellular and molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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

2 citing papers in PubMed.

  1. Article
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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

5 authors.

Yan LiuDepartment of Interventional Treatment, The Fifth People's Hospital of Chengdu, Chengdu, Sichuan, China.
Di DuDepartment of Interventional Treatment, The Fifth People's Hospital of Chengdu, Chengdu, Sichuan, China.
Xue GuDepartment of Interventional Treatment, The Fifth People's Hospital of Chengdu, Chengdu, Sichuan, China.
Qing HeDepartment of Interventional Treatment, The Fifth People's Hospital of Chengdu, Chengdu, Sichuan, China.
Bin XiongDepartment of Hepatobiliary Surgery, The People's Hospital of Tongnan District Chongqing city, Chongqing, China.ORCID 0009-0009-8347-3041

Funding

Chengdu University of Traditional Chinese Medicine "Xinglin Scholars" Discipline Talent Research Enhancement Program Hospital Special Project YYZX2021035National Natural Science Foundation of China 82003828National Natural Science Foundation of China 82100604Sichuan Province Traditional Chinese Medicine Management Traditional Chinese Medicine Research Special Project 2023MS322The Medical Research Projects in Chengdu City 2022275
6 · The paper itself

Abstract

Hepatocellular carcinoma (HCC) is a malignant tumour that poses a serious threat to human health and places a heavy burden on individuals and society. However, the role of GPC1 in the malignant progression of HCC is unknown. In this study, we analysed the expression of GPC1 in HCC, and its association with poor patient prognosis. The effects of GPC1 on the proliferation, invasion and migration of HCC were analysed through cellular functional experiments in vitro and in vivo. Mechanistically, DNA methylation of GPC1 was analysed by DNA extraction, methylation-specific PCR and bisulfite Sanger sequencing (BSP), and the target genes TET1 and miRNA regulating DNA methylation of GPC1 were found through the bioinformatics database. The results revealed that GPC1 was highly expressed in HCC, and its high expression was significantly associated with poor prognosis of HCC patients. Inhibiting the expression of GPC1 can inhibit the proliferation, invasion and migration of HCC cells. GPC1 was hypomethylated in HCC, and its methylation level was regulated by TET1. miR-143-3p can significantly regulated the expression of TET1 and affect the methylation level and protein expression of GPC1. Furthermore, GPC1 also affects the malignant biological behaviour of HCC by regulating the expression of Hippo signalling pathway. In summary, miR-143-3p regulates the expression of TET1, affects the expression of GPC1 through DNA methylation and regulates the malignant progression of HCC via Hippo signalling pathway.

Indexed as

Carcinoma, HepatocellularDNA MethylationGlypicansLiver NeoplasmsMicroRNAsMixed Function OxygenasesProtein Serine-Threonine KinasesProto-Oncogene ProteinsAnimalsCell Line, TumorCell MovementCell ProliferationFemaleGene Expression Regulation, NeoplasticHippo Signaling PathwayHumansGlypicansMicroRNAsMixed Function OxygenasesProtein Serine-Threonine KinasesProto-Oncogene ProteinsTET1 protein, human

Identifiers

PMID39823268
PMCPMC11740985

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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.