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Novel approaches in cancer treatment: preclinical and clinical development of small non-coding RNA therapeutics

Short or small interfering RNAs (siRNAs) and microRNA (miRNAs) are molecules similar in size and function able to inhibit gene expression based on their complementarity with mRNA sequences, inducing the degradation of the transcript or the inhibition of their translation. siRNAs bind specifically to...

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Autores principales: Cuciniello, Rossana, Filosa, Stefania, Crispi, Stefania
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642961/
https://www.ncbi.nlm.nih.gov/pubmed/34863235
http://dx.doi.org/10.1186/s13046-021-02193-1
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author Cuciniello, Rossana
Filosa, Stefania
Crispi, Stefania
author_facet Cuciniello, Rossana
Filosa, Stefania
Crispi, Stefania
author_sort Cuciniello, Rossana
collection PubMed
description Short or small interfering RNAs (siRNAs) and microRNA (miRNAs) are molecules similar in size and function able to inhibit gene expression based on their complementarity with mRNA sequences, inducing the degradation of the transcript or the inhibition of their translation. siRNAs bind specifically to a single gene location by sequence complementarity and regulate gene expression by specifically targeting transcription units via posttranscriptional gene silencing. miRNAs can regulate the expression of different gene targets through their imperfect base pairing. This process - known as RNA interference (RNAi) - modulates transcription in order to maintain a correct physiological environment, playing a role in almost the totality of the cellular pathways. siRNAs have been evolutionary evolved for the protection of genome integrity in response to exogenous and invasive nucleic acids such as transgenes or transposons. Artificial siRNAs are widely used in molecular biology for transient silencing of genes of interest. This strategy allows to inhibit the expression of any target protein of known sequence and is currently used for the treatment of different human diseases including cancer. Modifications and rearrangements in gene regions encoding for miRNAs have been found in cancer cells, and specific miRNA expression profiles characterize the developmental lineage and the differentiation state of the tumor. miRNAs with different expression patterns in tumors have been reported as oncogenes (oncomirs) or tumor-suppressors (anti-oncomirs). RNA modulation has become important in cancer research not only for development of early and easy diagnosis tools but also as a promising novel therapeutic approach. Despite the emerging discoveries supporting the role of miRNAs in carcinogenesis and their and siRNAs possible use in therapy, a series of concerns regarding their development, delivery and side effects have arisen. In this review we report the biology of miRNAs and siRNAs in relation to cancer summarizing the recent methods described to use them as novel therapeutic drugs and methods to specifically deliver them to cancer cells and overcome the limitations in the use of these molecules. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13046-021-02193-1.
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spelling pubmed-86429612021-12-06 Novel approaches in cancer treatment: preclinical and clinical development of small non-coding RNA therapeutics Cuciniello, Rossana Filosa, Stefania Crispi, Stefania J Exp Clin Cancer Res Review Short or small interfering RNAs (siRNAs) and microRNA (miRNAs) are molecules similar in size and function able to inhibit gene expression based on their complementarity with mRNA sequences, inducing the degradation of the transcript or the inhibition of their translation. siRNAs bind specifically to a single gene location by sequence complementarity and regulate gene expression by specifically targeting transcription units via posttranscriptional gene silencing. miRNAs can regulate the expression of different gene targets through their imperfect base pairing. This process - known as RNA interference (RNAi) - modulates transcription in order to maintain a correct physiological environment, playing a role in almost the totality of the cellular pathways. siRNAs have been evolutionary evolved for the protection of genome integrity in response to exogenous and invasive nucleic acids such as transgenes or transposons. Artificial siRNAs are widely used in molecular biology for transient silencing of genes of interest. This strategy allows to inhibit the expression of any target protein of known sequence and is currently used for the treatment of different human diseases including cancer. Modifications and rearrangements in gene regions encoding for miRNAs have been found in cancer cells, and specific miRNA expression profiles characterize the developmental lineage and the differentiation state of the tumor. miRNAs with different expression patterns in tumors have been reported as oncogenes (oncomirs) or tumor-suppressors (anti-oncomirs). RNA modulation has become important in cancer research not only for development of early and easy diagnosis tools but also as a promising novel therapeutic approach. Despite the emerging discoveries supporting the role of miRNAs in carcinogenesis and their and siRNAs possible use in therapy, a series of concerns regarding their development, delivery and side effects have arisen. In this review we report the biology of miRNAs and siRNAs in relation to cancer summarizing the recent methods described to use them as novel therapeutic drugs and methods to specifically deliver them to cancer cells and overcome the limitations in the use of these molecules. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13046-021-02193-1. BioMed Central 2021-12-04 /pmc/articles/PMC8642961/ /pubmed/34863235 http://dx.doi.org/10.1186/s13046-021-02193-1 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Cuciniello, Rossana
Filosa, Stefania
Crispi, Stefania
Novel approaches in cancer treatment: preclinical and clinical development of small non-coding RNA therapeutics
title Novel approaches in cancer treatment: preclinical and clinical development of small non-coding RNA therapeutics
title_full Novel approaches in cancer treatment: preclinical and clinical development of small non-coding RNA therapeutics
title_fullStr Novel approaches in cancer treatment: preclinical and clinical development of small non-coding RNA therapeutics
title_full_unstemmed Novel approaches in cancer treatment: preclinical and clinical development of small non-coding RNA therapeutics
title_short Novel approaches in cancer treatment: preclinical and clinical development of small non-coding RNA therapeutics
title_sort novel approaches in cancer treatment: preclinical and clinical development of small non-coding rna therapeutics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8642961/
https://www.ncbi.nlm.nih.gov/pubmed/34863235
http://dx.doi.org/10.1186/s13046-021-02193-1
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