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miR-372 inhibits p62 in head and neck squamous cell carcinoma in vitro and in vivo
Here we showed that exogenous miR-372 expression and knockdown of p62 (sequestosome1 or SQSTM1), both increased migration of head and neck squamous cell carcinoma (HNSCC) cells. p62 induced phase II detoxification enzyme NADPH quinone oxidoreductase 1 (NQO1), which decreased ROS levels and cell migr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467422/ https://www.ncbi.nlm.nih.gov/pubmed/25714028 |
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author | Yeh, Li-Yin Liu, Chung-Ji Wong, Yong-Kie Chang, Christine Lin, Shu-Chun Chang, Kuo-Wei |
author_facet | Yeh, Li-Yin Liu, Chung-Ji Wong, Yong-Kie Chang, Christine Lin, Shu-Chun Chang, Kuo-Wei |
author_sort | Yeh, Li-Yin |
collection | PubMed |
description | Here we showed that exogenous miR-372 expression and knockdown of p62 (sequestosome1 or SQSTM1), both increased migration of head and neck squamous cell carcinoma (HNSCC) cells. p62 induced phase II detoxification enzyme NADPH quinone oxidoreductase 1 (NQO1), which decreased ROS levels and cell migration. Also, miR-372 decreased p62 during hypoxia, thus increasing cell migration. Levels of miR-372 and p62 inversely correlated in human HNSCC tissues. Plasma levels of miR-372 was associated with advanced tumor stage and patient mortality. Both plasma and salivary miR-372 levels were decreased after tumor resection. We conclude that miR-372 decreases p62, thus increasing ROS and motility in HNSCC cells. |
format | Online Article Text |
id | pubmed-4467422 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-44674222015-06-22 miR-372 inhibits p62 in head and neck squamous cell carcinoma in vitro and in vivo Yeh, Li-Yin Liu, Chung-Ji Wong, Yong-Kie Chang, Christine Lin, Shu-Chun Chang, Kuo-Wei Oncotarget Research Paper Here we showed that exogenous miR-372 expression and knockdown of p62 (sequestosome1 or SQSTM1), both increased migration of head and neck squamous cell carcinoma (HNSCC) cells. p62 induced phase II detoxification enzyme NADPH quinone oxidoreductase 1 (NQO1), which decreased ROS levels and cell migration. Also, miR-372 decreased p62 during hypoxia, thus increasing cell migration. Levels of miR-372 and p62 inversely correlated in human HNSCC tissues. Plasma levels of miR-372 was associated with advanced tumor stage and patient mortality. Both plasma and salivary miR-372 levels were decreased after tumor resection. We conclude that miR-372 decreases p62, thus increasing ROS and motility in HNSCC cells. Impact Journals LLC 2015-01-21 /pmc/articles/PMC4467422/ /pubmed/25714028 Text en Copyright: © 2015 Yeh et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Yeh, Li-Yin Liu, Chung-Ji Wong, Yong-Kie Chang, Christine Lin, Shu-Chun Chang, Kuo-Wei miR-372 inhibits p62 in head and neck squamous cell carcinoma in vitro and in vivo |
title | miR-372 inhibits p62 in head and neck squamous cell carcinoma in vitro and in vivo |
title_full | miR-372 inhibits p62 in head and neck squamous cell carcinoma in vitro and in vivo |
title_fullStr | miR-372 inhibits p62 in head and neck squamous cell carcinoma in vitro and in vivo |
title_full_unstemmed | miR-372 inhibits p62 in head and neck squamous cell carcinoma in vitro and in vivo |
title_short | miR-372 inhibits p62 in head and neck squamous cell carcinoma in vitro and in vivo |
title_sort | mir-372 inhibits p62 in head and neck squamous cell carcinoma in vitro and in vivo |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4467422/ https://www.ncbi.nlm.nih.gov/pubmed/25714028 |
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