Evidence map›Paper›PMID 39523083›Full record

ArticleNan fang yi ke da xue xue bao = Journal of Southern Medical University2024

[Inhibiting Yes-associated protein alleviates CCl

W Zhao, H Ruan, S Wang, Y Cheng, M Lei, J Zhao, C Liu

Abstract readEnglish Abstract
In one paragraph

Article in Nan fang yi ke da xue xue bao = Journal of Southern Medical University, 2024. 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

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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

7 authors.

W ZhaoDepartment of Infectious Diseases, First Affiliated Hospital of Bengbu Medical University, Bengbu 233000, China.
H RuanDepartment of Infectious Diseases, First Affiliated Hospital of Bengbu Medical University, Bengbu 233000, China.
S WangDepartment of Infectious Diseases, First Affiliated Hospital of Bengbu Medical University, Bengbu 233000, China.
Y ChengDepartment of Infectious Diseases, First Affiliated Hospital of Bengbu Medical University, Bengbu 233000, China.
M LeiDepartment of Infectious Diseases, First Affiliated Hospital of Bengbu Medical University, Bengbu 233000, China.
J ZhaoDepartment of Infectious Diseases, First Affiliated Hospital of Bengbu Medical University, Bengbu 233000, China.
C LiuDepartment of Infectious Diseases, First Affiliated Hospital of Bengbu Medical University, Bengbu 233000, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo explore whether Yes-associated protein (YAP) affects occurrence and progression of liver fibrosis by regulating epithelial-mesenchymal transition (EMT).

methodsIn a 8-week-old C57BL/6 mouse model of CCl

resultsThe mouse models of liver fibrosis showed obvious structural damages of the liver lobes with formation of pseudolobules, and verteporfin treatment significantly improved these pathologies and lowered plasma ALT and AST levels of the mice. Transcriptome and proteomic sequencing and informatics analysis suggested that N-cadherin and Twist were differentially expressed in liver fibrosis in close correlation with YAP. Inhibition of YAP obviously downregulated hepatic N-cadherin and Twist protein expressions in the mice with liver fibrosis. In patients with CHB and liver cirrhosis, serum levels of YAP elevated obviously with the severity of liver fibrosis and were significantly correlated with N-cadherin, vimentin and Twist levels. In mice with liver fibrosis, inhibiting Twist effectively improved liver inflammation and fibrosis, while the combined treatment with YAP activator worsened hepatic collagen fiber deposition and increased hepatic YAP and

conclusionEMT is an important pathogenic mechanism of liver fibrosis, and inhibiting YAP can alleviate liver fibrosis by reducing EMT.

Indexed as

Carbon TetrachlorideEpithelial-Mesenchymal TransitionLiver CirrhosisMice, Inbred C57BLYAP-Signaling ProteinsAdaptor Proteins, Signal TransducingAnimalsCadherinsDisease Models, AnimalHepatitis B, ChronicHumansLiverMaleMiceProteomicsTranscription FactorsAdaptor Proteins, Signal TransducingCadherinsCarbon TetrachlorideTranscription FactorsTwist-Related Protein 1VerteporfinVimentinYap1 protein, mouseYAP-Signaling Proteinsbiomarkersepithelial mesenchymal transitionliver fibrosisYes-associated protein

Identifiers

PMID39523083
PMCPMC11526463

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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.