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Interplay of non-coding RNAs and approved antimetabolites such as gemcitabine and pemetrexed in mesothelioma

Gemcitabine and pemetrexed are clinically approved antimetabolites for the therapy of mesothelioma diseases. These drugs are often applied in combination with platinum complexes and other drugs. The activity of antimetabolites depended on the expression levels of certain non-coding RNAs, in particul...

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Autor principal: Biersack, Bernhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: KeAi Publishing 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257890/
https://www.ncbi.nlm.nih.gov/pubmed/30809600
http://dx.doi.org/10.1016/j.ncrna.2018.11.001
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author Biersack, Bernhard
author_facet Biersack, Bernhard
author_sort Biersack, Bernhard
collection PubMed
description Gemcitabine and pemetrexed are clinically approved antimetabolites for the therapy of mesothelioma diseases. These drugs are often applied in combination with platinum complexes and other drugs. The activity of antimetabolites depended on the expression levels of certain non-coding RNAs, in particular, of small microRNAs (miRNAs) and long non-coding RNAs (lncRNAs). The development of tumor resistance towards antimetabolites was regulated by non-coding RNAs. An overview of the interplay between gemcitabine/pemetrexed antimetabolites and non-coding RNAs in mesothelioma is provided. Further to this, various non-coding RNA-modulating agents are discussed which displayed positive effects on gemcitabine or pemetrexed treatment of mesothelioma diseases. A detailed knowledge of the connections of non-coding RNAs with antimetabolites will be constructive for the design of improved therapies in future.
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spelling pubmed-62578902019-02-26 Interplay of non-coding RNAs and approved antimetabolites such as gemcitabine and pemetrexed in mesothelioma Biersack, Bernhard Noncoding RNA Res Article Gemcitabine and pemetrexed are clinically approved antimetabolites for the therapy of mesothelioma diseases. These drugs are often applied in combination with platinum complexes and other drugs. The activity of antimetabolites depended on the expression levels of certain non-coding RNAs, in particular, of small microRNAs (miRNAs) and long non-coding RNAs (lncRNAs). The development of tumor resistance towards antimetabolites was regulated by non-coding RNAs. An overview of the interplay between gemcitabine/pemetrexed antimetabolites and non-coding RNAs in mesothelioma is provided. Further to this, various non-coding RNA-modulating agents are discussed which displayed positive effects on gemcitabine or pemetrexed treatment of mesothelioma diseases. A detailed knowledge of the connections of non-coding RNAs with antimetabolites will be constructive for the design of improved therapies in future. KeAi Publishing 2018-11-04 /pmc/articles/PMC6257890/ /pubmed/30809600 http://dx.doi.org/10.1016/j.ncrna.2018.11.001 Text en . http://creativecommons.org/licenses/BY-NC-ND/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/BY-NC-ND/4.0/).
spellingShingle Article
Biersack, Bernhard
Interplay of non-coding RNAs and approved antimetabolites such as gemcitabine and pemetrexed in mesothelioma
title Interplay of non-coding RNAs and approved antimetabolites such as gemcitabine and pemetrexed in mesothelioma
title_full Interplay of non-coding RNAs and approved antimetabolites such as gemcitabine and pemetrexed in mesothelioma
title_fullStr Interplay of non-coding RNAs and approved antimetabolites such as gemcitabine and pemetrexed in mesothelioma
title_full_unstemmed Interplay of non-coding RNAs and approved antimetabolites such as gemcitabine and pemetrexed in mesothelioma
title_short Interplay of non-coding RNAs and approved antimetabolites such as gemcitabine and pemetrexed in mesothelioma
title_sort interplay of non-coding rnas and approved antimetabolites such as gemcitabine and pemetrexed in mesothelioma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6257890/
https://www.ncbi.nlm.nih.gov/pubmed/30809600
http://dx.doi.org/10.1016/j.ncrna.2018.11.001
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