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Development of a 5-FU modified miR-129 mimic as a therapeutic for non-small cell lung cancer

Lung cancer is the leading cause of cancer-related deaths in the United States with non-small cell lung cancer (NSCLC) accounting for most cases. Despite advances in cancer therapeutics, the 5-year survival rate has remained poor due to several contributing factors, including its resistance to thera...

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Autores principales: Hwang, Ga-Ram, Yuen, John G., Fesler, Andrew, Farley, Hannah, Haley, John D., Ju, Jingfang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995506/
https://www.ncbi.nlm.nih.gov/pubmed/36911069
http://dx.doi.org/10.1016/j.omto.2023.02.007
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author Hwang, Ga-Ram
Yuen, John G.
Fesler, Andrew
Farley, Hannah
Haley, John D.
Ju, Jingfang
author_facet Hwang, Ga-Ram
Yuen, John G.
Fesler, Andrew
Farley, Hannah
Haley, John D.
Ju, Jingfang
author_sort Hwang, Ga-Ram
collection PubMed
description Lung cancer is the leading cause of cancer-related deaths in the United States with non-small cell lung cancer (NSCLC) accounting for most cases. Despite advances in cancer therapeutics, the 5-year survival rate has remained poor due to several contributing factors, including its resistance to therapeutics. Therefore, there is a pressing need to develop therapeutics that can overcome resistance. Non-coding RNAs, including microRNAs (miRNAs), have been found to contribute to cancer resistance and therapeutics by modulating the expression of several targets involving multiple key mechanisms. In this study, we investigated the therapeutic potential of miR-129 modified with 5-fluorouracil (5-FU) in NSCLC. Our results show that 5-FU modified miR-129 (5-FU-miR-129) inhibits proliferation, induces apoptosis, and retains function as an miRNA in NSCLC cell lines A549 and Calu-1. Notably, we observed that 5-FU-miR-129 was able to overcome resistance to tyrosine kinase inhibitors and chemotherapy in cell lines resistant to erlotinib or 5-FU. Furthermore, we observed that the inhibitory effect of 5-FU-miR-129 can also be achieved in NSCLC cells under vehicle-free conditions. Finally, 5-FU-miR-129 inhibited NSCLC tumor growth and extended survival in vivo without toxic side effects. Altogether, our results demonstrate the potential of 5-FU-miR-129 as a highly potent cancer therapeutic in NSCLC.
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spelling pubmed-99955062023-03-10 Development of a 5-FU modified miR-129 mimic as a therapeutic for non-small cell lung cancer Hwang, Ga-Ram Yuen, John G. Fesler, Andrew Farley, Hannah Haley, John D. Ju, Jingfang Mol Ther Oncolytics Original Article Lung cancer is the leading cause of cancer-related deaths in the United States with non-small cell lung cancer (NSCLC) accounting for most cases. Despite advances in cancer therapeutics, the 5-year survival rate has remained poor due to several contributing factors, including its resistance to therapeutics. Therefore, there is a pressing need to develop therapeutics that can overcome resistance. Non-coding RNAs, including microRNAs (miRNAs), have been found to contribute to cancer resistance and therapeutics by modulating the expression of several targets involving multiple key mechanisms. In this study, we investigated the therapeutic potential of miR-129 modified with 5-fluorouracil (5-FU) in NSCLC. Our results show that 5-FU modified miR-129 (5-FU-miR-129) inhibits proliferation, induces apoptosis, and retains function as an miRNA in NSCLC cell lines A549 and Calu-1. Notably, we observed that 5-FU-miR-129 was able to overcome resistance to tyrosine kinase inhibitors and chemotherapy in cell lines resistant to erlotinib or 5-FU. Furthermore, we observed that the inhibitory effect of 5-FU-miR-129 can also be achieved in NSCLC cells under vehicle-free conditions. Finally, 5-FU-miR-129 inhibited NSCLC tumor growth and extended survival in vivo without toxic side effects. Altogether, our results demonstrate the potential of 5-FU-miR-129 as a highly potent cancer therapeutic in NSCLC. American Society of Gene & Cell Therapy 2023-02-17 /pmc/articles/PMC9995506/ /pubmed/36911069 http://dx.doi.org/10.1016/j.omto.2023.02.007 Text en © 2023 The Authors. https://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 Original Article
Hwang, Ga-Ram
Yuen, John G.
Fesler, Andrew
Farley, Hannah
Haley, John D.
Ju, Jingfang
Development of a 5-FU modified miR-129 mimic as a therapeutic for non-small cell lung cancer
title Development of a 5-FU modified miR-129 mimic as a therapeutic for non-small cell lung cancer
title_full Development of a 5-FU modified miR-129 mimic as a therapeutic for non-small cell lung cancer
title_fullStr Development of a 5-FU modified miR-129 mimic as a therapeutic for non-small cell lung cancer
title_full_unstemmed Development of a 5-FU modified miR-129 mimic as a therapeutic for non-small cell lung cancer
title_short Development of a 5-FU modified miR-129 mimic as a therapeutic for non-small cell lung cancer
title_sort development of a 5-fu modified mir-129 mimic as a therapeutic for non-small cell lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995506/
https://www.ncbi.nlm.nih.gov/pubmed/36911069
http://dx.doi.org/10.1016/j.omto.2023.02.007
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