Cargando…
MicroRNA-31: a pivotal oncogenic factor in oral squamous cell carcinoma
Oral squamous cell carcinoma (OSCC) continuously constitutes a major challenge for treatment and prognosis due to approximately half of treated OSCC patients dying from locoregional recurrences and distant metastases. MicroRNA-31 (miR-31), an early mammalian miRNA identified, has been gaining import...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964740/ https://www.ncbi.nlm.nih.gov/pubmed/35351880 http://dx.doi.org/10.1038/s41420-022-00948-z |
_version_ | 1784678284989038592 |
---|---|
author | Lin, Xiaojiao Wu, Weizhou Ying, Yukang Luo, Jun Xu, Xuhui Zheng, Linxia Wu, Weili Yang, Suqing Zhao, Shankun |
author_facet | Lin, Xiaojiao Wu, Weizhou Ying, Yukang Luo, Jun Xu, Xuhui Zheng, Linxia Wu, Weili Yang, Suqing Zhao, Shankun |
author_sort | Lin, Xiaojiao |
collection | PubMed |
description | Oral squamous cell carcinoma (OSCC) continuously constitutes a major challenge for treatment and prognosis due to approximately half of treated OSCC patients dying from locoregional recurrences and distant metastases. MicroRNA-31 (miR-31), an early mammalian miRNA identified, has been gaining importance in the field of OSCC research in recent years. This comprehensive review was conducted for the first time to summarize the current evidence on the association between miR-31 and OSCC. The vast majority of relevant studies (20/21, 95%) demonstrated that miR-31 was an oncogenic factor in the tumorigenesis and progression of OSCC. miR-31 expression is significantly upregulated in plasma, saliva, and tumor tissue of OSCC. miR-31 played an essential role in OSCC development by constituting a complex network with its targeted genes (e.g. RhoA, FIH, ACOX1, VEGF, SIRT3, LATS2, KANK1, and NUMB) and the signaling cascades (e.g. EGF-AKT signaling axis, ERK-MMP9 cascade, Hippo pathway, Wnt signaling, and MCT1/MCT4 regulatory cascade). This review highlights that miR-31 might function as a potential diagnostic, prognostic, and predictive biomarker for OSCC. Further studies are still warranted to better illuminate the clinicopathological features and the molecular mechanisms of miR-31-mediated OSCC development. |
format | Online Article Text |
id | pubmed-8964740 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-89647402022-04-12 MicroRNA-31: a pivotal oncogenic factor in oral squamous cell carcinoma Lin, Xiaojiao Wu, Weizhou Ying, Yukang Luo, Jun Xu, Xuhui Zheng, Linxia Wu, Weili Yang, Suqing Zhao, Shankun Cell Death Discov Review Article Oral squamous cell carcinoma (OSCC) continuously constitutes a major challenge for treatment and prognosis due to approximately half of treated OSCC patients dying from locoregional recurrences and distant metastases. MicroRNA-31 (miR-31), an early mammalian miRNA identified, has been gaining importance in the field of OSCC research in recent years. This comprehensive review was conducted for the first time to summarize the current evidence on the association between miR-31 and OSCC. The vast majority of relevant studies (20/21, 95%) demonstrated that miR-31 was an oncogenic factor in the tumorigenesis and progression of OSCC. miR-31 expression is significantly upregulated in plasma, saliva, and tumor tissue of OSCC. miR-31 played an essential role in OSCC development by constituting a complex network with its targeted genes (e.g. RhoA, FIH, ACOX1, VEGF, SIRT3, LATS2, KANK1, and NUMB) and the signaling cascades (e.g. EGF-AKT signaling axis, ERK-MMP9 cascade, Hippo pathway, Wnt signaling, and MCT1/MCT4 regulatory cascade). This review highlights that miR-31 might function as a potential diagnostic, prognostic, and predictive biomarker for OSCC. Further studies are still warranted to better illuminate the clinicopathological features and the molecular mechanisms of miR-31-mediated OSCC development. Nature Publishing Group UK 2022-03-29 /pmc/articles/PMC8964740/ /pubmed/35351880 http://dx.doi.org/10.1038/s41420-022-00948-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Review Article Lin, Xiaojiao Wu, Weizhou Ying, Yukang Luo, Jun Xu, Xuhui Zheng, Linxia Wu, Weili Yang, Suqing Zhao, Shankun MicroRNA-31: a pivotal oncogenic factor in oral squamous cell carcinoma |
title | MicroRNA-31: a pivotal oncogenic factor in oral squamous cell carcinoma |
title_full | MicroRNA-31: a pivotal oncogenic factor in oral squamous cell carcinoma |
title_fullStr | MicroRNA-31: a pivotal oncogenic factor in oral squamous cell carcinoma |
title_full_unstemmed | MicroRNA-31: a pivotal oncogenic factor in oral squamous cell carcinoma |
title_short | MicroRNA-31: a pivotal oncogenic factor in oral squamous cell carcinoma |
title_sort | microrna-31: a pivotal oncogenic factor in oral squamous cell carcinoma |
topic | Review Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8964740/ https://www.ncbi.nlm.nih.gov/pubmed/35351880 http://dx.doi.org/10.1038/s41420-022-00948-z |
work_keys_str_mv | AT linxiaojiao microrna31apivotaloncogenicfactorinoralsquamouscellcarcinoma AT wuweizhou microrna31apivotaloncogenicfactorinoralsquamouscellcarcinoma AT yingyukang microrna31apivotaloncogenicfactorinoralsquamouscellcarcinoma AT luojun microrna31apivotaloncogenicfactorinoralsquamouscellcarcinoma AT xuxuhui microrna31apivotaloncogenicfactorinoralsquamouscellcarcinoma AT zhenglinxia microrna31apivotaloncogenicfactorinoralsquamouscellcarcinoma AT wuweili microrna31apivotaloncogenicfactorinoralsquamouscellcarcinoma AT yangsuqing microrna31apivotaloncogenicfactorinoralsquamouscellcarcinoma AT zhaoshankun microrna31apivotaloncogenicfactorinoralsquamouscellcarcinoma |