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Effect of Hypoxia-Induced Micro-RNAs Expression on Oncogenesis
MicroRNAs (miRNAs) are small non-coding RNAs that negatively regulate gene expression at the post-transcriptional level. An aberrant regulation of gene expression by miRNAs is associated with numerous diseases, including cancer. MiRNAs expression can be influenced by various stimuli, among which hyp...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9181687/ https://www.ncbi.nlm.nih.gov/pubmed/35682972 http://dx.doi.org/10.3390/ijms23116294 |
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author | Moriondo, Giorgia Scioscia, Giulia Soccio, Piera Tondo, Pasquale De Pace, Cosimo Carlo Sabato, Roberto Foschino Barbaro, Maria Pia Lacedonia, Donato |
author_facet | Moriondo, Giorgia Scioscia, Giulia Soccio, Piera Tondo, Pasquale De Pace, Cosimo Carlo Sabato, Roberto Foschino Barbaro, Maria Pia Lacedonia, Donato |
author_sort | Moriondo, Giorgia |
collection | PubMed |
description | MicroRNAs (miRNAs) are small non-coding RNAs that negatively regulate gene expression at the post-transcriptional level. An aberrant regulation of gene expression by miRNAs is associated with numerous diseases, including cancer. MiRNAs expression can be influenced by various stimuli, among which hypoxia; however, the effects of different types of continuous hypoxia (moderate or marked) on miRNAs are still poorly studied. Lately, some hypoxia-inducible miRNAs (HRMs, hypoxia-regulated miRNAs) have been identified. These HRMs are often activated in different types of cancers, suggesting their role in tumorigenesis. The aim of this study was to evaluate changes in miRNAs expression both in moderate continuous hypoxia and marked continuous hypoxia to better understand the possible relationship between hypoxia, miRNAs, and colorectal cancer. We used RT-PCR to detect the miRNAs expression in colorectal cancer cell lines in conditions of moderate and marked continuous hypoxia. The expression of miRNAs was analyzed using a two-way ANOVA test to compare the differential expression of miRNAs among groups. The levels of almost all analyzed miRNAs (miR-21, miR-23b, miR-26a, miR-27b, and miR-145) were greater in moderate hypoxia versus marked hypoxia, except for miR-23b and miR-21. This study identified a series of miRNAs involved in the response to different types of continuous hypoxia (moderate and marked), highlighting that they play a role in the development of cancer. To date, there are no other studies that demonstrate how these two types of continuous hypoxia could be able to activate different molecular pathways that lead to a different expression of specific miRNAs involved in tumorigenesis. |
format | Online Article Text |
id | pubmed-9181687 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-91816872022-06-10 Effect of Hypoxia-Induced Micro-RNAs Expression on Oncogenesis Moriondo, Giorgia Scioscia, Giulia Soccio, Piera Tondo, Pasquale De Pace, Cosimo Carlo Sabato, Roberto Foschino Barbaro, Maria Pia Lacedonia, Donato Int J Mol Sci Communication MicroRNAs (miRNAs) are small non-coding RNAs that negatively regulate gene expression at the post-transcriptional level. An aberrant regulation of gene expression by miRNAs is associated with numerous diseases, including cancer. MiRNAs expression can be influenced by various stimuli, among which hypoxia; however, the effects of different types of continuous hypoxia (moderate or marked) on miRNAs are still poorly studied. Lately, some hypoxia-inducible miRNAs (HRMs, hypoxia-regulated miRNAs) have been identified. These HRMs are often activated in different types of cancers, suggesting their role in tumorigenesis. The aim of this study was to evaluate changes in miRNAs expression both in moderate continuous hypoxia and marked continuous hypoxia to better understand the possible relationship between hypoxia, miRNAs, and colorectal cancer. We used RT-PCR to detect the miRNAs expression in colorectal cancer cell lines in conditions of moderate and marked continuous hypoxia. The expression of miRNAs was analyzed using a two-way ANOVA test to compare the differential expression of miRNAs among groups. The levels of almost all analyzed miRNAs (miR-21, miR-23b, miR-26a, miR-27b, and miR-145) were greater in moderate hypoxia versus marked hypoxia, except for miR-23b and miR-21. This study identified a series of miRNAs involved in the response to different types of continuous hypoxia (moderate and marked), highlighting that they play a role in the development of cancer. To date, there are no other studies that demonstrate how these two types of continuous hypoxia could be able to activate different molecular pathways that lead to a different expression of specific miRNAs involved in tumorigenesis. MDPI 2022-06-04 /pmc/articles/PMC9181687/ /pubmed/35682972 http://dx.doi.org/10.3390/ijms23116294 Text en © 2022 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 | Communication Moriondo, Giorgia Scioscia, Giulia Soccio, Piera Tondo, Pasquale De Pace, Cosimo Carlo Sabato, Roberto Foschino Barbaro, Maria Pia Lacedonia, Donato Effect of Hypoxia-Induced Micro-RNAs Expression on Oncogenesis |
title | Effect of Hypoxia-Induced Micro-RNAs Expression on Oncogenesis |
title_full | Effect of Hypoxia-Induced Micro-RNAs Expression on Oncogenesis |
title_fullStr | Effect of Hypoxia-Induced Micro-RNAs Expression on Oncogenesis |
title_full_unstemmed | Effect of Hypoxia-Induced Micro-RNAs Expression on Oncogenesis |
title_short | Effect of Hypoxia-Induced Micro-RNAs Expression on Oncogenesis |
title_sort | effect of hypoxia-induced micro-rnas expression on oncogenesis |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9181687/ https://www.ncbi.nlm.nih.gov/pubmed/35682972 http://dx.doi.org/10.3390/ijms23116294 |
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