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Targeting miR-185-3p Inhibits Head and Neck Squamous Cell Carcinoma by Modulating RAB25

Cancer cell-derived exosomes regulate tumor growth and progression. However, the effects of exosomes and its contents on head and neck squamous cell carcinoma (HNSCC) and its underlying mechanisms remain unclear. Here, we found HNSCC displayed a dysregulation of exosomes biogenesis. miR-185-3p was o...

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Detalles Bibliográficos
Autores principales: Wang, Xueping, Zhu, Xiaoyuan, Zhao, Yulin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634093/
https://www.ncbi.nlm.nih.gov/pubmed/34868916
http://dx.doi.org/10.3389/fonc.2021.721416
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author Wang, Xueping
Zhu, Xiaoyuan
Zhao, Yulin
author_facet Wang, Xueping
Zhu, Xiaoyuan
Zhao, Yulin
author_sort Wang, Xueping
collection PubMed
description Cancer cell-derived exosomes regulate tumor growth and progression. However, the effects of exosomes and its contents on head and neck squamous cell carcinoma (HNSCC) and its underlying mechanisms remain unclear. Here, we found HNSCC displayed a dysregulation of exosomes biogenesis. miR-185-3p was one of the most upregulated exosome-derived miRNAs in HNSCC. Functional assay showed that RAB25 is a direct downstream target of miR-185-3p. miR-185-3p/RAB25 signaling controlled tumor progression and correlated with disease prognosis. Targeting miR-185-3p/RAB25 significantly inhibited tumor growth and promoted drug response to chemotherapy. To conclude, the findings demonstrate exosomal miR-185-3p promotes tumor growth by mediating RAB25 that could be effectively targeted for HNSCC treatment.
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spelling pubmed-86340932021-12-02 Targeting miR-185-3p Inhibits Head and Neck Squamous Cell Carcinoma by Modulating RAB25 Wang, Xueping Zhu, Xiaoyuan Zhao, Yulin Front Oncol Oncology Cancer cell-derived exosomes regulate tumor growth and progression. However, the effects of exosomes and its contents on head and neck squamous cell carcinoma (HNSCC) and its underlying mechanisms remain unclear. Here, we found HNSCC displayed a dysregulation of exosomes biogenesis. miR-185-3p was one of the most upregulated exosome-derived miRNAs in HNSCC. Functional assay showed that RAB25 is a direct downstream target of miR-185-3p. miR-185-3p/RAB25 signaling controlled tumor progression and correlated with disease prognosis. Targeting miR-185-3p/RAB25 significantly inhibited tumor growth and promoted drug response to chemotherapy. To conclude, the findings demonstrate exosomal miR-185-3p promotes tumor growth by mediating RAB25 that could be effectively targeted for HNSCC treatment. Frontiers Media S.A. 2021-11-15 /pmc/articles/PMC8634093/ /pubmed/34868916 http://dx.doi.org/10.3389/fonc.2021.721416 Text en Copyright © 2021 Wang, Zhu and Zhao https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Wang, Xueping
Zhu, Xiaoyuan
Zhao, Yulin
Targeting miR-185-3p Inhibits Head and Neck Squamous Cell Carcinoma by Modulating RAB25
title Targeting miR-185-3p Inhibits Head and Neck Squamous Cell Carcinoma by Modulating RAB25
title_full Targeting miR-185-3p Inhibits Head and Neck Squamous Cell Carcinoma by Modulating RAB25
title_fullStr Targeting miR-185-3p Inhibits Head and Neck Squamous Cell Carcinoma by Modulating RAB25
title_full_unstemmed Targeting miR-185-3p Inhibits Head and Neck Squamous Cell Carcinoma by Modulating RAB25
title_short Targeting miR-185-3p Inhibits Head and Neck Squamous Cell Carcinoma by Modulating RAB25
title_sort targeting mir-185-3p inhibits head and neck squamous cell carcinoma by modulating rab25
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8634093/
https://www.ncbi.nlm.nih.gov/pubmed/34868916
http://dx.doi.org/10.3389/fonc.2021.721416
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