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Pinin Induces Epithelial-to-Mesenchymal Transition in Hepatocellular Carcinoma by Regulating m6A Modification
Pinin is a moonlighting protein localized in desmosomes and nucleus. It could promote the growth of hepatocellular carcinoma. Whether this protein can induce epithelial-to-mesenchymal transition (EMT) and malignant progression in HCC is unknown. This work found that Pinin prompts EMT in vitro and in...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8670902/ https://www.ncbi.nlm.nih.gov/pubmed/34917148 http://dx.doi.org/10.1155/2021/7529164 |
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author | Qiao, Kailiang Chen, Caihong Liu, Haoyang Qin, Yuan Liu, Huijuan |
author_facet | Qiao, Kailiang Chen, Caihong Liu, Haoyang Qin, Yuan Liu, Huijuan |
author_sort | Qiao, Kailiang |
collection | PubMed |
description | Pinin is a moonlighting protein localized in desmosomes and nucleus. It could promote the growth of hepatocellular carcinoma. Whether this protein can induce epithelial-to-mesenchymal transition (EMT) and malignant progression in HCC is unknown. This work found that Pinin prompts EMT in vitro and in vivo. Further mechanism study found that Pinin increases the level of N6-methyladenosine (m6A) modification of RNA by interacting with METTL3, which in turn induces snail1 expression. These findings suggest that Pinin induces EMT by regulating m6A modification and, thus, could be a potential anticancer target for HCC therapy. |
format | Online Article Text |
id | pubmed-8670902 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-86709022021-12-15 Pinin Induces Epithelial-to-Mesenchymal Transition in Hepatocellular Carcinoma by Regulating m6A Modification Qiao, Kailiang Chen, Caihong Liu, Haoyang Qin, Yuan Liu, Huijuan J Oncol Research Article Pinin is a moonlighting protein localized in desmosomes and nucleus. It could promote the growth of hepatocellular carcinoma. Whether this protein can induce epithelial-to-mesenchymal transition (EMT) and malignant progression in HCC is unknown. This work found that Pinin prompts EMT in vitro and in vivo. Further mechanism study found that Pinin increases the level of N6-methyladenosine (m6A) modification of RNA by interacting with METTL3, which in turn induces snail1 expression. These findings suggest that Pinin induces EMT by regulating m6A modification and, thus, could be a potential anticancer target for HCC therapy. Hindawi 2021-12-07 /pmc/articles/PMC8670902/ /pubmed/34917148 http://dx.doi.org/10.1155/2021/7529164 Text en Copyright © 2021 Kailiang Qiao et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Qiao, Kailiang Chen, Caihong Liu, Haoyang Qin, Yuan Liu, Huijuan Pinin Induces Epithelial-to-Mesenchymal Transition in Hepatocellular Carcinoma by Regulating m6A Modification |
title | Pinin Induces Epithelial-to-Mesenchymal Transition in Hepatocellular Carcinoma by Regulating m6A Modification |
title_full | Pinin Induces Epithelial-to-Mesenchymal Transition in Hepatocellular Carcinoma by Regulating m6A Modification |
title_fullStr | Pinin Induces Epithelial-to-Mesenchymal Transition in Hepatocellular Carcinoma by Regulating m6A Modification |
title_full_unstemmed | Pinin Induces Epithelial-to-Mesenchymal Transition in Hepatocellular Carcinoma by Regulating m6A Modification |
title_short | Pinin Induces Epithelial-to-Mesenchymal Transition in Hepatocellular Carcinoma by Regulating m6A Modification |
title_sort | pinin induces epithelial-to-mesenchymal transition in hepatocellular carcinoma by regulating m6a modification |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8670902/ https://www.ncbi.nlm.nih.gov/pubmed/34917148 http://dx.doi.org/10.1155/2021/7529164 |
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