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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2022
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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. |
format | Online Article Text |
id | pubmed-9812005 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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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