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Autophagy in cancers including brain tumors: role of MicroRNAs

Autophagy has a crucial role in many cancers, including brain tumors. Several types of endogenous molecules (e.g. microRNAs, AKT, PTEN, p53, EGFR, and NF1) can modulate the process of autophagy. Recently miRNAs (small non-coding RNAs) have been found to play a vital role in the regulation of differe...

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Autores principales: Pourhanifeh, Mohammad Hossein, Mahjoubin-Tehran, Maryam, Karimzadeh, Mohammad Reza, Mirzaei, Hamid Reza, Razavi, Zahra Sadat, Sahebkar, Amirhossein, Hosseini, Nayyerehsadat, Mirzaei, Hamed, Hamblin, Michael R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285723/
https://www.ncbi.nlm.nih.gov/pubmed/32517694
http://dx.doi.org/10.1186/s12964-020-00587-w
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author Pourhanifeh, Mohammad Hossein
Mahjoubin-Tehran, Maryam
Karimzadeh, Mohammad Reza
Mirzaei, Hamid Reza
Razavi, Zahra Sadat
Sahebkar, Amirhossein
Hosseini, Nayyerehsadat
Mirzaei, Hamed
Hamblin, Michael R.
author_facet Pourhanifeh, Mohammad Hossein
Mahjoubin-Tehran, Maryam
Karimzadeh, Mohammad Reza
Mirzaei, Hamid Reza
Razavi, Zahra Sadat
Sahebkar, Amirhossein
Hosseini, Nayyerehsadat
Mirzaei, Hamed
Hamblin, Michael R.
author_sort Pourhanifeh, Mohammad Hossein
collection PubMed
description Autophagy has a crucial role in many cancers, including brain tumors. Several types of endogenous molecules (e.g. microRNAs, AKT, PTEN, p53, EGFR, and NF1) can modulate the process of autophagy. Recently miRNAs (small non-coding RNAs) have been found to play a vital role in the regulation of different cellular and molecular processes, such as autophagy. Deregulation of these molecules is associated with the development and progression of different pathological conditions, including brain tumors. It was found that miRNAs are epigenetic regulators, which influence the level of proteins coded by the targeted mRNAs with any modification of the genetic sequences. It has been revealed that various miRNAs (e.g., miR-7-1-3p, miR-340, miR-17, miR-30a, miR-224-3p, and miR-93), as epigenetic regulators, can modulate autophagy pathways within brain tumors. A deeper understanding of the underlying molecular targets of miRNAs, and their function in autophagy pathways could contribute to the development of new treatment methods for patients with brain tumors. In this review, we summarize the various miRNAs, which are involved in regulating autophagy in brain tumors. Moreover, we highlight the role of miRNAs in autophagy-related pathways in different cancers.
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spelling pubmed-72857232020-06-11 Autophagy in cancers including brain tumors: role of MicroRNAs Pourhanifeh, Mohammad Hossein Mahjoubin-Tehran, Maryam Karimzadeh, Mohammad Reza Mirzaei, Hamid Reza Razavi, Zahra Sadat Sahebkar, Amirhossein Hosseini, Nayyerehsadat Mirzaei, Hamed Hamblin, Michael R. Cell Commun Signal Review Autophagy has a crucial role in many cancers, including brain tumors. Several types of endogenous molecules (e.g. microRNAs, AKT, PTEN, p53, EGFR, and NF1) can modulate the process of autophagy. Recently miRNAs (small non-coding RNAs) have been found to play a vital role in the regulation of different cellular and molecular processes, such as autophagy. Deregulation of these molecules is associated with the development and progression of different pathological conditions, including brain tumors. It was found that miRNAs are epigenetic regulators, which influence the level of proteins coded by the targeted mRNAs with any modification of the genetic sequences. It has been revealed that various miRNAs (e.g., miR-7-1-3p, miR-340, miR-17, miR-30a, miR-224-3p, and miR-93), as epigenetic regulators, can modulate autophagy pathways within brain tumors. A deeper understanding of the underlying molecular targets of miRNAs, and their function in autophagy pathways could contribute to the development of new treatment methods for patients with brain tumors. In this review, we summarize the various miRNAs, which are involved in regulating autophagy in brain tumors. Moreover, we highlight the role of miRNAs in autophagy-related pathways in different cancers. BioMed Central 2020-06-09 /pmc/articles/PMC7285723/ /pubmed/32517694 http://dx.doi.org/10.1186/s12964-020-00587-w Text en © The Author(s) 2020 Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Pourhanifeh, Mohammad Hossein
Mahjoubin-Tehran, Maryam
Karimzadeh, Mohammad Reza
Mirzaei, Hamid Reza
Razavi, Zahra Sadat
Sahebkar, Amirhossein
Hosseini, Nayyerehsadat
Mirzaei, Hamed
Hamblin, Michael R.
Autophagy in cancers including brain tumors: role of MicroRNAs
title Autophagy in cancers including brain tumors: role of MicroRNAs
title_full Autophagy in cancers including brain tumors: role of MicroRNAs
title_fullStr Autophagy in cancers including brain tumors: role of MicroRNAs
title_full_unstemmed Autophagy in cancers including brain tumors: role of MicroRNAs
title_short Autophagy in cancers including brain tumors: role of MicroRNAs
title_sort autophagy in cancers including brain tumors: role of micrornas
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7285723/
https://www.ncbi.nlm.nih.gov/pubmed/32517694
http://dx.doi.org/10.1186/s12964-020-00587-w
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