MicroRNAs-Role in Lung Cancer
Regulation of gene expression is essential for normal physiological functions; thus deregulation of gene expression is common in disease conditions. One level of regulation of gene expression is performed by noncoding RNAs, among which microRNAs (miRNA) are the best studied. Abnormal expression of t...
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2014
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Online Access: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972902/ |
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pubmed-39729022014-04-17 MicroRNAs-Role in Lung Cancer Guz, Małgorzata Rivero-Müller, Adolfo Okoń, Estera Stenzel-Bembenek, Agnieszka Polberg, Krzysztof Słomka, Maria Stepulak, Andrzej Review Article Regulation of gene expression is essential for normal physiological functions; thus deregulation of gene expression is common in disease conditions. One level of regulation of gene expression is performed by noncoding RNAs, among which microRNAs (miRNA) are the best studied. Abnormal expression of these molecular players can lead to pathogenic processes such as heart disease, immune system abnormalities, and carcinogenesis, to name but a few. Of a length of 18–25 nucleotides miRNAs are involved in binding partial complementary sequences within the 3′-UTR (3′-untranslated region) of the target mRNAs. Depending on the type of neoplastic transformation, miRNAs can act both as oncogenes (oncomirs) or as tumor suppressors. Because of the great importance of miRNAs, most researches focus on either their role as biomarkers or their potential as therapeutic targets. Herein, we present the review of microRNA biology, function, and tumorigenic potential with emphasis on their role in lung cancer. Hindawi Publishing Corporation 2014 2014-03-13 /pmc/articles/PMC3972902/ /pubmed/24744457 http://dx.doi.org/10.1155/2014/218169 Text en Copyright © 2014 Małgorzata Guz et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
repository_type |
Open Access Journal |
institution_category |
Foreign Institution |
institution |
US National Center for Biotechnology Information |
building |
NCBI PubMed |
collection |
Online Access |
language |
English |
format |
Online |
author |
Guz, Małgorzata Rivero-Müller, Adolfo Okoń, Estera Stenzel-Bembenek, Agnieszka Polberg, Krzysztof Słomka, Maria Stepulak, Andrzej |
spellingShingle |
Guz, Małgorzata Rivero-Müller, Adolfo Okoń, Estera Stenzel-Bembenek, Agnieszka Polberg, Krzysztof Słomka, Maria Stepulak, Andrzej MicroRNAs-Role in Lung Cancer |
author_facet |
Guz, Małgorzata Rivero-Müller, Adolfo Okoń, Estera Stenzel-Bembenek, Agnieszka Polberg, Krzysztof Słomka, Maria Stepulak, Andrzej |
author_sort |
Guz, Małgorzata |
title |
MicroRNAs-Role in Lung Cancer |
title_short |
MicroRNAs-Role in Lung Cancer |
title_full |
MicroRNAs-Role in Lung Cancer |
title_fullStr |
MicroRNAs-Role in Lung Cancer |
title_full_unstemmed |
MicroRNAs-Role in Lung Cancer |
title_sort |
micrornas-role in lung cancer |
description |
Regulation of gene expression is essential for normal physiological functions; thus deregulation of gene expression is common in disease conditions. One level of regulation of gene expression is performed by noncoding RNAs, among which microRNAs (miRNA) are the best studied. Abnormal expression of these molecular players can lead to pathogenic processes such as heart disease, immune system abnormalities, and carcinogenesis, to name but a few. Of a length of 18–25 nucleotides miRNAs are involved in binding partial complementary sequences within the 3′-UTR (3′-untranslated region) of the target mRNAs. Depending on the type of neoplastic transformation, miRNAs can act both as oncogenes (oncomirs) or as tumor suppressors. Because of the great importance of miRNAs, most researches focus on either their role as biomarkers or their potential as therapeutic targets. Herein, we present the review of microRNA biology, function, and tumorigenic potential with emphasis on their role in lung cancer. |
publisher |
Hindawi Publishing Corporation |
publishDate |
2014 |
url |
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3972902/ |
_version_ |
1612073227009392640 |