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CircRNA-Associated CeRNAs Regulatory Axes in Retinoblastoma: A Systematic Scoping Review

Retinoblastoma (RB) is one of the most common childhood cancers caused by RB gene mutations (tumor suppressor gene in various patients). A better understanding of molecular pathways and the development of new diagnostic approaches may lead to better treatment for RB patients. The number of studies o...

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Autores principales: Asadi, Mohammad Reza, Moslehian, Marziyeh Sadat, Sabaie, Hani, Sharifi-Bonab, Mirmohsen, Hakimi, Parvin, Hussen, Bashdar Mahmud, Taheri, Mohammad, Rakhshan, Azadeh, Rezazadeh, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294360/
https://www.ncbi.nlm.nih.gov/pubmed/35865469
http://dx.doi.org/10.3389/fonc.2022.910470
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author Asadi, Mohammad Reza
Moslehian, Marziyeh Sadat
Sabaie, Hani
Sharifi-Bonab, Mirmohsen
Hakimi, Parvin
Hussen, Bashdar Mahmud
Taheri, Mohammad
Rakhshan, Azadeh
Rezazadeh, Maryam
author_facet Asadi, Mohammad Reza
Moslehian, Marziyeh Sadat
Sabaie, Hani
Sharifi-Bonab, Mirmohsen
Hakimi, Parvin
Hussen, Bashdar Mahmud
Taheri, Mohammad
Rakhshan, Azadeh
Rezazadeh, Maryam
author_sort Asadi, Mohammad Reza
collection PubMed
description Retinoblastoma (RB) is one of the most common childhood cancers caused by RB gene mutations (tumor suppressor gene in various patients). A better understanding of molecular pathways and the development of new diagnostic approaches may lead to better treatment for RB patients. The number of studies on ceRNA axes is increasing, emphasizing the significance of these axes in RB. Circular RNAs (circRNAs) play a vital role in competing endogenous RNA (ceRNA) regulatory axes by sponging microRNAs and regulating gene expression. Because of the broadness of ceRNA interaction networks, they may assist in investigating treatment targets in RB. This study conducted a systematic scoping review to evaluate verified loops of ceRNA in RB, focusing on the ceRNA axis and its relationship to circRNAs. This scoping review was carried out using a six-step strategy and the Prisma guideline, and it involved systematically searching the publications of seven databases. Out of 363 records, sixteen articles were entirely consistent with the defined inclusion criteria and were summarized in the relevant table. The majority of the studies focused on the circRNAs circ_0000527, circ_0000034, and circTET1, with approximately two-fifths of the studies focusing on a single circRNA. Understanding the many features of this regulatory structure may help elucidate RB’s unknown causative factors and provide novel molecular potential therapeutic targets and medical fields.
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spelling pubmed-92943602022-07-20 CircRNA-Associated CeRNAs Regulatory Axes in Retinoblastoma: A Systematic Scoping Review Asadi, Mohammad Reza Moslehian, Marziyeh Sadat Sabaie, Hani Sharifi-Bonab, Mirmohsen Hakimi, Parvin Hussen, Bashdar Mahmud Taheri, Mohammad Rakhshan, Azadeh Rezazadeh, Maryam Front Oncol Oncology Retinoblastoma (RB) is one of the most common childhood cancers caused by RB gene mutations (tumor suppressor gene in various patients). A better understanding of molecular pathways and the development of new diagnostic approaches may lead to better treatment for RB patients. The number of studies on ceRNA axes is increasing, emphasizing the significance of these axes in RB. Circular RNAs (circRNAs) play a vital role in competing endogenous RNA (ceRNA) regulatory axes by sponging microRNAs and regulating gene expression. Because of the broadness of ceRNA interaction networks, they may assist in investigating treatment targets in RB. This study conducted a systematic scoping review to evaluate verified loops of ceRNA in RB, focusing on the ceRNA axis and its relationship to circRNAs. This scoping review was carried out using a six-step strategy and the Prisma guideline, and it involved systematically searching the publications of seven databases. Out of 363 records, sixteen articles were entirely consistent with the defined inclusion criteria and were summarized in the relevant table. The majority of the studies focused on the circRNAs circ_0000527, circ_0000034, and circTET1, with approximately two-fifths of the studies focusing on a single circRNA. Understanding the many features of this regulatory structure may help elucidate RB’s unknown causative factors and provide novel molecular potential therapeutic targets and medical fields. Frontiers Media S.A. 2022-07-05 /pmc/articles/PMC9294360/ /pubmed/35865469 http://dx.doi.org/10.3389/fonc.2022.910470 Text en Copyright © 2022 Asadi, Moslehian, Sabaie, Sharifi-Bonab, Hakimi, Hussen, Taheri, Rakhshan and Rezazadeh 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
Asadi, Mohammad Reza
Moslehian, Marziyeh Sadat
Sabaie, Hani
Sharifi-Bonab, Mirmohsen
Hakimi, Parvin
Hussen, Bashdar Mahmud
Taheri, Mohammad
Rakhshan, Azadeh
Rezazadeh, Maryam
CircRNA-Associated CeRNAs Regulatory Axes in Retinoblastoma: A Systematic Scoping Review
title CircRNA-Associated CeRNAs Regulatory Axes in Retinoblastoma: A Systematic Scoping Review
title_full CircRNA-Associated CeRNAs Regulatory Axes in Retinoblastoma: A Systematic Scoping Review
title_fullStr CircRNA-Associated CeRNAs Regulatory Axes in Retinoblastoma: A Systematic Scoping Review
title_full_unstemmed CircRNA-Associated CeRNAs Regulatory Axes in Retinoblastoma: A Systematic Scoping Review
title_short CircRNA-Associated CeRNAs Regulatory Axes in Retinoblastoma: A Systematic Scoping Review
title_sort circrna-associated cernas regulatory axes in retinoblastoma: a systematic scoping review
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9294360/
https://www.ncbi.nlm.nih.gov/pubmed/35865469
http://dx.doi.org/10.3389/fonc.2022.910470
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