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The Role of Micro RNAs in Regulating PI3K/AKT Signaling Pathways in Glioblastoma

Glioblastoma is a type of brain cancer with aggressive and invasive nature. Such features result from increased proliferation and migration and also poor apoptosis of glioma cells leading to resistance to current treatments such as chemotherapy and radiotherapy. In recent studies, micro RNAs have be...

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Autores principales: Ghaffarian Zirak, Roshanak, Tajik, Hurie, Asadi, Jahanbakhsh, Hashemian, Pedram, Javid, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Iranian Society of Pathology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013863/
https://www.ncbi.nlm.nih.gov/pubmed/35463721
http://dx.doi.org/10.30699/IJP.2022.539029.2726
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author Ghaffarian Zirak, Roshanak
Tajik, Hurie
Asadi, Jahanbakhsh
Hashemian, Pedram
Javid, Hossein
author_facet Ghaffarian Zirak, Roshanak
Tajik, Hurie
Asadi, Jahanbakhsh
Hashemian, Pedram
Javid, Hossein
author_sort Ghaffarian Zirak, Roshanak
collection PubMed
description Glioblastoma is a type of brain cancer with aggressive and invasive nature. Such features result from increased proliferation and migration and also poor apoptosis of glioma cells leading to resistance to current treatments such as chemotherapy and radiotherapy. In recent studies, micro RNAs have been introduced as a novel target for treating glioblastoma via regulation of apoptotic signaling pathway, remarkably PI3K/AKT, which affect cellular functions and blockage or progression of the tumor. In this review, we focus on PI3K/AKT signaling pathway and other related apoptotic processes contributing to glioblastoma and investigate the role of micro RNAs interfering in apoptosis, invasion and proliferation of glioma through such apoptotic processes pathways. Databases NCBI, PubMed, and Web of Science were searched for published English articles using keywords such as 'miRNA OR microRNA', 'Glioblastoma', 'apoptotic pathways', 'PI3K and AKT', 'Caspase signaling Pathway' and 'Notch pathway'. Most articles were published from 7 May 2015 to 16 June 2020. This study focused on PI3K/AKT signaling pathway affecting glioma cells in separated subparts. Also, other related apoptotic pathways as the Caspase cycle and Notch have been also investigated. Nearly 40 miRNAs were found as tumor suppressors or onco-miRNA, and their targets, which regulated subcomponents participating in proliferation, invasion, and apoptosis of the tumoral cells. Our review reveals that miRNAs affect key molecules in signaling apoptotic pathways, partly PI3K/AKT, making them potential therapeutic targets to overcome the tumor. However, their utility as a novel treatment for glioblastoma requires further examination and investigation.
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spelling pubmed-90138632022-04-22 The Role of Micro RNAs in Regulating PI3K/AKT Signaling Pathways in Glioblastoma Ghaffarian Zirak, Roshanak Tajik, Hurie Asadi, Jahanbakhsh Hashemian, Pedram Javid, Hossein Iran J Pathol Review Article Glioblastoma is a type of brain cancer with aggressive and invasive nature. Such features result from increased proliferation and migration and also poor apoptosis of glioma cells leading to resistance to current treatments such as chemotherapy and radiotherapy. In recent studies, micro RNAs have been introduced as a novel target for treating glioblastoma via regulation of apoptotic signaling pathway, remarkably PI3K/AKT, which affect cellular functions and blockage or progression of the tumor. In this review, we focus on PI3K/AKT signaling pathway and other related apoptotic processes contributing to glioblastoma and investigate the role of micro RNAs interfering in apoptosis, invasion and proliferation of glioma through such apoptotic processes pathways. Databases NCBI, PubMed, and Web of Science were searched for published English articles using keywords such as 'miRNA OR microRNA', 'Glioblastoma', 'apoptotic pathways', 'PI3K and AKT', 'Caspase signaling Pathway' and 'Notch pathway'. Most articles were published from 7 May 2015 to 16 June 2020. This study focused on PI3K/AKT signaling pathway affecting glioma cells in separated subparts. Also, other related apoptotic pathways as the Caspase cycle and Notch have been also investigated. Nearly 40 miRNAs were found as tumor suppressors or onco-miRNA, and their targets, which regulated subcomponents participating in proliferation, invasion, and apoptosis of the tumoral cells. Our review reveals that miRNAs affect key molecules in signaling apoptotic pathways, partly PI3K/AKT, making them potential therapeutic targets to overcome the tumor. However, their utility as a novel treatment for glioblastoma requires further examination and investigation. Iranian Society of Pathology 2022 2022-03-08 /pmc/articles/PMC9013863/ /pubmed/35463721 http://dx.doi.org/10.30699/IJP.2022.539029.2726 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Ghaffarian Zirak, Roshanak
Tajik, Hurie
Asadi, Jahanbakhsh
Hashemian, Pedram
Javid, Hossein
The Role of Micro RNAs in Regulating PI3K/AKT Signaling Pathways in Glioblastoma
title The Role of Micro RNAs in Regulating PI3K/AKT Signaling Pathways in Glioblastoma
title_full The Role of Micro RNAs in Regulating PI3K/AKT Signaling Pathways in Glioblastoma
title_fullStr The Role of Micro RNAs in Regulating PI3K/AKT Signaling Pathways in Glioblastoma
title_full_unstemmed The Role of Micro RNAs in Regulating PI3K/AKT Signaling Pathways in Glioblastoma
title_short The Role of Micro RNAs in Regulating PI3K/AKT Signaling Pathways in Glioblastoma
title_sort role of micro rnas in regulating pi3k/akt signaling pathways in glioblastoma
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9013863/
https://www.ncbi.nlm.nih.gov/pubmed/35463721
http://dx.doi.org/10.30699/IJP.2022.539029.2726
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