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Circular RNA as a Potential Biomarker for Melanoma: A Systematic Review

Circular RNAs (circRNAs) are newly discovered RNAs with covalently looped structures. Due to their resistance to RNAase degradation and tissue-specific expression, circRNAs are expected to be potential biomarkers in early diagnosis and target treatment of many diseases. However, the role of circRNAs...

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Autores principales: Tang, Keyun, Zhang, Hanlin, Li, Yaqi, Sun, Qiuning, Jin, Hongzhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047128/
https://www.ncbi.nlm.nih.gov/pubmed/33869186
http://dx.doi.org/10.3389/fcell.2021.638548
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author Tang, Keyun
Zhang, Hanlin
Li, Yaqi
Sun, Qiuning
Jin, Hongzhong
author_facet Tang, Keyun
Zhang, Hanlin
Li, Yaqi
Sun, Qiuning
Jin, Hongzhong
author_sort Tang, Keyun
collection PubMed
description Circular RNAs (circRNAs) are newly discovered RNAs with covalently looped structures. Due to their resistance to RNAase degradation and tissue-specific expression, circRNAs are expected to be potential biomarkers in early diagnosis and target treatment of many diseases. However, the role of circRNAs in melanoma still needs to be systematically reviewed for better understanding and further research. Based on published articles in PubMed, Embase, Cochrane Library, and Web of Science database, we systematically reviewed the implications and recent advances of circRNAs in melanoma, focusing on function, mechanism, and correlation with melanoma progression. According to inclusion and exclusion criteria, a total of 19 articles were finally included in this systematic review. Of the 19 studies, 17 used human samples, including melanoma tissues (n = 16) and blood serum of patients with melanoma (n = 1). The sample size of the study group ranged from 20 to 105 based on the reported data. Several studies explored the association between circRNAs and clinicopathological characteristics. circRNA dysregulation was commonly observed in melanoma patients. circRNAs function in melanoma by miRNA sponging and interaction with RNA binding proteins (RBP), ultimately controlling several important signaling pathways and cancer-related cellular processes, including proliferation, migration, invasion, metastasis, apoptosis, and glucose metabolism. circRNA expression could be associated with prognostic factors and drug responses, consolidating the potential clinical value in melanoma. Herein, we clarified the functional, prognostic, and predictive roles of circRNAs in melanoma in this systematic review, providing future directions for studies on melanoma-associated circRNAs.
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spelling pubmed-80471282021-04-16 Circular RNA as a Potential Biomarker for Melanoma: A Systematic Review Tang, Keyun Zhang, Hanlin Li, Yaqi Sun, Qiuning Jin, Hongzhong Front Cell Dev Biol Cell and Developmental Biology Circular RNAs (circRNAs) are newly discovered RNAs with covalently looped structures. Due to their resistance to RNAase degradation and tissue-specific expression, circRNAs are expected to be potential biomarkers in early diagnosis and target treatment of many diseases. However, the role of circRNAs in melanoma still needs to be systematically reviewed for better understanding and further research. Based on published articles in PubMed, Embase, Cochrane Library, and Web of Science database, we systematically reviewed the implications and recent advances of circRNAs in melanoma, focusing on function, mechanism, and correlation with melanoma progression. According to inclusion and exclusion criteria, a total of 19 articles were finally included in this systematic review. Of the 19 studies, 17 used human samples, including melanoma tissues (n = 16) and blood serum of patients with melanoma (n = 1). The sample size of the study group ranged from 20 to 105 based on the reported data. Several studies explored the association between circRNAs and clinicopathological characteristics. circRNA dysregulation was commonly observed in melanoma patients. circRNAs function in melanoma by miRNA sponging and interaction with RNA binding proteins (RBP), ultimately controlling several important signaling pathways and cancer-related cellular processes, including proliferation, migration, invasion, metastasis, apoptosis, and glucose metabolism. circRNA expression could be associated with prognostic factors and drug responses, consolidating the potential clinical value in melanoma. Herein, we clarified the functional, prognostic, and predictive roles of circRNAs in melanoma in this systematic review, providing future directions for studies on melanoma-associated circRNAs. Frontiers Media S.A. 2021-04-01 /pmc/articles/PMC8047128/ /pubmed/33869186 http://dx.doi.org/10.3389/fcell.2021.638548 Text en Copyright © 2021 Tang, Zhang, Li, Sun and Jin. 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 Cell and Developmental Biology
Tang, Keyun
Zhang, Hanlin
Li, Yaqi
Sun, Qiuning
Jin, Hongzhong
Circular RNA as a Potential Biomarker for Melanoma: A Systematic Review
title Circular RNA as a Potential Biomarker for Melanoma: A Systematic Review
title_full Circular RNA as a Potential Biomarker for Melanoma: A Systematic Review
title_fullStr Circular RNA as a Potential Biomarker for Melanoma: A Systematic Review
title_full_unstemmed Circular RNA as a Potential Biomarker for Melanoma: A Systematic Review
title_short Circular RNA as a Potential Biomarker for Melanoma: A Systematic Review
title_sort circular rna as a potential biomarker for melanoma: a systematic review
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8047128/
https://www.ncbi.nlm.nih.gov/pubmed/33869186
http://dx.doi.org/10.3389/fcell.2021.638548
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