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Inverse Impact of Cancer Drugs on Circular and Linear RNAs in Breast Cancer Cell Lines

Altered expression of circular RNAs (circRNAs) has previously been investigated in breast cancer. However, little is known about the effects of drugs on their regulation and relationship with the cognate linear transcript (linRNA). We analyzed the dysregulation of both 12 cancer-related circRNAs and...

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Autores principales: Terrazzan, Anna, Crudele, Francesca, Corrà, Fabio, Ancona, Pietro, Palatini, Jeffrey, Bianchi, Nicoletta, Volinia, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204552/
https://www.ncbi.nlm.nih.gov/pubmed/37218992
http://dx.doi.org/10.3390/ncrna9030032
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author Terrazzan, Anna
Crudele, Francesca
Corrà, Fabio
Ancona, Pietro
Palatini, Jeffrey
Bianchi, Nicoletta
Volinia, Stefano
author_facet Terrazzan, Anna
Crudele, Francesca
Corrà, Fabio
Ancona, Pietro
Palatini, Jeffrey
Bianchi, Nicoletta
Volinia, Stefano
author_sort Terrazzan, Anna
collection PubMed
description Altered expression of circular RNAs (circRNAs) has previously been investigated in breast cancer. However, little is known about the effects of drugs on their regulation and relationship with the cognate linear transcript (linRNA). We analyzed the dysregulation of both 12 cancer-related circRNAs and their linRNAs in two breast cancer cell lines undergoing various treatments. We selected 14 well-known anticancer agents affecting different cellular pathways and examined their impact. Upon drug exposure circRNA/linRNA expression ratios increased, as a result of the downregulation of linRNA and upregulation of circRNA within the same gene. In this study, we highlighted the relevance of identifying the drug-regulated circ/linRNAs according to their oncogenic or anticancer role. Interestingly, VRK1 and MAN1A2 were increased by several drugs in both cell lines. However, they display opposite effects, circ/linVRK1 favors apoptosis whereas circ/linMAN1A2 stimulates cell migration, and only XL765 did not alter the ratio of other dangerous circ/linRNAs in MCF-7. In MDA-MB-231 cells, AMG511 and GSK1070916 decreased circGFRA1, as a good response to drugs. Furthermore, some circRNAs might be associated with specific mutated pathways, such as the PI3K/AKT in MCF-7 cells with circ/linHIPK3 correlating to cancer progression and drug-resistance, or NHEJ DNA repair pathway in TP-53 mutated MDA-MB-231 cells.
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spelling pubmed-102045522023-05-24 Inverse Impact of Cancer Drugs on Circular and Linear RNAs in Breast Cancer Cell Lines Terrazzan, Anna Crudele, Francesca Corrà, Fabio Ancona, Pietro Palatini, Jeffrey Bianchi, Nicoletta Volinia, Stefano Noncoding RNA Article Altered expression of circular RNAs (circRNAs) has previously been investigated in breast cancer. However, little is known about the effects of drugs on their regulation and relationship with the cognate linear transcript (linRNA). We analyzed the dysregulation of both 12 cancer-related circRNAs and their linRNAs in two breast cancer cell lines undergoing various treatments. We selected 14 well-known anticancer agents affecting different cellular pathways and examined their impact. Upon drug exposure circRNA/linRNA expression ratios increased, as a result of the downregulation of linRNA and upregulation of circRNA within the same gene. In this study, we highlighted the relevance of identifying the drug-regulated circ/linRNAs according to their oncogenic or anticancer role. Interestingly, VRK1 and MAN1A2 were increased by several drugs in both cell lines. However, they display opposite effects, circ/linVRK1 favors apoptosis whereas circ/linMAN1A2 stimulates cell migration, and only XL765 did not alter the ratio of other dangerous circ/linRNAs in MCF-7. In MDA-MB-231 cells, AMG511 and GSK1070916 decreased circGFRA1, as a good response to drugs. Furthermore, some circRNAs might be associated with specific mutated pathways, such as the PI3K/AKT in MCF-7 cells with circ/linHIPK3 correlating to cancer progression and drug-resistance, or NHEJ DNA repair pathway in TP-53 mutated MDA-MB-231 cells. MDPI 2023-05-19 /pmc/articles/PMC10204552/ /pubmed/37218992 http://dx.doi.org/10.3390/ncrna9030032 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Terrazzan, Anna
Crudele, Francesca
Corrà, Fabio
Ancona, Pietro
Palatini, Jeffrey
Bianchi, Nicoletta
Volinia, Stefano
Inverse Impact of Cancer Drugs on Circular and Linear RNAs in Breast Cancer Cell Lines
title Inverse Impact of Cancer Drugs on Circular and Linear RNAs in Breast Cancer Cell Lines
title_full Inverse Impact of Cancer Drugs on Circular and Linear RNAs in Breast Cancer Cell Lines
title_fullStr Inverse Impact of Cancer Drugs on Circular and Linear RNAs in Breast Cancer Cell Lines
title_full_unstemmed Inverse Impact of Cancer Drugs on Circular and Linear RNAs in Breast Cancer Cell Lines
title_short Inverse Impact of Cancer Drugs on Circular and Linear RNAs in Breast Cancer Cell Lines
title_sort inverse impact of cancer drugs on circular and linear rnas in breast cancer cell lines
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10204552/
https://www.ncbi.nlm.nih.gov/pubmed/37218992
http://dx.doi.org/10.3390/ncrna9030032
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