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Modulation of Genes and MicroRNAs in the Neurospheres of Glioblastoma Cell Lines U343 and T98G Induced by Ionizing Radiation and Temozolomide Therapy

Introduction: Glioblastoma is the most prevalent primary malignant neoplasm of the central nervous system. It has increased its incidence, while the overall survival remains over 14 months. Purpose: The purpose is to evaluate the expression of the genes EGFR, PTEN, MGMT, and IDH1/2, and microRNAs mi...

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Autores principales: Da Costa Almeida, Thiago L, Rodrigues, Andressa R, Cirino, Múcio, Trevisan, Felipe A, Peria, Fernanda, Tirapelli, Daniela, Carlotti Jr, Carlos Gilberto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812005/
https://www.ncbi.nlm.nih.gov/pubmed/36620850
http://dx.doi.org/10.7759/cureus.32211
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author Da Costa Almeida, Thiago L
Rodrigues, Andressa R
Cirino, Múcio
Trevisan, Felipe A
Peria, Fernanda
Tirapelli, Daniela
Carlotti Jr, Carlos Gilberto
author_facet Da Costa Almeida, Thiago L
Rodrigues, Andressa R
Cirino, Múcio
Trevisan, Felipe A
Peria, Fernanda
Tirapelli, Daniela
Carlotti Jr, Carlos Gilberto
author_sort Da Costa Almeida, Thiago L
collection PubMed
description Introduction: Glioblastoma is the most prevalent primary malignant neoplasm of the central nervous system. It has increased its incidence, while the overall survival remains over 14 months. Purpose: The purpose is to evaluate the expression of the genes EGFR, PTEN, MGMT, and IDH1/2, and microRNAs miR-181b, miR-145, miR-149, and miR-128a in adhered cells (AC) and neurospheres (NS) from cell lines (T98G and U343) submitted to temozolomide (TMZ) and ionizing radiation (IR). Methods: T98G and U343 were treated with TMZ, IR, and TMZ+IR. The analysis of gene expression and miRNAs was performed using real-time PCR. Results: This study demonstrated: a) an improvement in the expression of IDH1 after IR and TMZ + IR in the NS (T98G); b) an increase in the expression of MGMT in NS (T98G) in IR groups and TMZ + IR. The expression of miRNAs results as a) AC (U343) expressed more miR-181b after TMZ, IR, and TMZ + IR; and miR-128a improved after TMZ, IR, and TMZ + IR; b) NS (T98G) after TMZ + IR expressed: miR-181b; miR-149; miR-145 and miR-128a; c) NS (U343) after IR huge expressed miR-149 and miR-145. Conclusion: IR was an independent and determining radioresistance factor in NS. However, we observed no complementarity action of oncomiRs regulation.
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spelling pubmed-98120052023-01-05 Modulation of Genes and MicroRNAs in the Neurospheres of Glioblastoma Cell Lines U343 and T98G Induced by Ionizing Radiation and Temozolomide Therapy Da Costa Almeida, Thiago L Rodrigues, Andressa R Cirino, Múcio Trevisan, Felipe A Peria, Fernanda Tirapelli, Daniela Carlotti Jr, Carlos Gilberto Cureus Genetics Introduction: Glioblastoma is the most prevalent primary malignant neoplasm of the central nervous system. It has increased its incidence, while the overall survival remains over 14 months. Purpose: The purpose is to evaluate the expression of the genes EGFR, PTEN, MGMT, and IDH1/2, and microRNAs miR-181b, miR-145, miR-149, and miR-128a in adhered cells (AC) and neurospheres (NS) from cell lines (T98G and U343) submitted to temozolomide (TMZ) and ionizing radiation (IR). Methods: T98G and U343 were treated with TMZ, IR, and TMZ+IR. The analysis of gene expression and miRNAs was performed using real-time PCR. Results: This study demonstrated: a) an improvement in the expression of IDH1 after IR and TMZ + IR in the NS (T98G); b) an increase in the expression of MGMT in NS (T98G) in IR groups and TMZ + IR. The expression of miRNAs results as a) AC (U343) expressed more miR-181b after TMZ, IR, and TMZ + IR; and miR-128a improved after TMZ, IR, and TMZ + IR; b) NS (T98G) after TMZ + IR expressed: miR-181b; miR-149; miR-145 and miR-128a; c) NS (U343) after IR huge expressed miR-149 and miR-145. Conclusion: IR was an independent and determining radioresistance factor in NS. However, we observed no complementarity action of oncomiRs regulation. Cureus 2022-12-05 /pmc/articles/PMC9812005/ /pubmed/36620850 http://dx.doi.org/10.7759/cureus.32211 Text en Copyright © 2022, Da Costa Almeida et al. https://creativecommons.org/licenses/by/3.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Genetics
Da Costa Almeida, Thiago L
Rodrigues, Andressa R
Cirino, Múcio
Trevisan, Felipe A
Peria, Fernanda
Tirapelli, Daniela
Carlotti Jr, Carlos Gilberto
Modulation of Genes and MicroRNAs in the Neurospheres of Glioblastoma Cell Lines U343 and T98G Induced by Ionizing Radiation and Temozolomide Therapy
title Modulation of Genes and MicroRNAs in the Neurospheres of Glioblastoma Cell Lines U343 and T98G Induced by Ionizing Radiation and Temozolomide Therapy
title_full Modulation of Genes and MicroRNAs in the Neurospheres of Glioblastoma Cell Lines U343 and T98G Induced by Ionizing Radiation and Temozolomide Therapy
title_fullStr Modulation of Genes and MicroRNAs in the Neurospheres of Glioblastoma Cell Lines U343 and T98G Induced by Ionizing Radiation and Temozolomide Therapy
title_full_unstemmed Modulation of Genes and MicroRNAs in the Neurospheres of Glioblastoma Cell Lines U343 and T98G Induced by Ionizing Radiation and Temozolomide Therapy
title_short Modulation of Genes and MicroRNAs in the Neurospheres of Glioblastoma Cell Lines U343 and T98G Induced by Ionizing Radiation and Temozolomide Therapy
title_sort modulation of genes and micrornas in the neurospheres of glioblastoma cell lines u343 and t98g induced by ionizing radiation and temozolomide therapy
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9812005/
https://www.ncbi.nlm.nih.gov/pubmed/36620850
http://dx.doi.org/10.7759/cureus.32211
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