Cargando…

Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy

MicroRNAs (miRNAs) are endogenous small noncoding RNAs that negatively regulate gene expression by interfering with the translation or stability of target transcripts. Some tumor-suppressive miRNAs can concurrently target multiple cancer-promoting genes and may be useful as therapeutic anticancer ag...

Descripción completa

Detalles Bibliográficos
Autores principales: Gokita, Kentaro, Inoue, Jun, Ishihara, Hiroshi, Kojima, Kazuyuki, Inazawa, Johji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society of Gene & Cell Therapy 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938807/
https://www.ncbi.nlm.nih.gov/pubmed/31877409
http://dx.doi.org/10.1016/j.omtn.2019.10.045
_version_ 1783484104953561088
author Gokita, Kentaro
Inoue, Jun
Ishihara, Hiroshi
Kojima, Kazuyuki
Inazawa, Johji
author_facet Gokita, Kentaro
Inoue, Jun
Ishihara, Hiroshi
Kojima, Kazuyuki
Inazawa, Johji
author_sort Gokita, Kentaro
collection PubMed
description MicroRNAs (miRNAs) are endogenous small noncoding RNAs that negatively regulate gene expression by interfering with the translation or stability of target transcripts. Some tumor-suppressive miRNAs can concurrently target multiple cancer-promoting genes and may be useful as therapeutic anticancer agents. However, the development of drug delivery systems is critical for the implementation of miRNA-based therapeutics. We have previously demonstrated that the enforced expression of miR-634 effectively induces apoptosis by concurrently and directly targeting genes associated with mitochondrial homeostasis, antiapoptosis signaling, antioxidant ability, and autophagy in cancer cells. In the current study, we validated the therapeutic potential of lipid nanoparticle (LNP)-mediated delivery of miR-634 for cancer therapy. We confirmed the ability of enforced expression of miR-634 to induce apoptosis in various cancer cell lines, including pancreatic cancer cells. Intravenous administration of LNPs harboring miR-634 significantly reduced the xenograft tumor growth of BxPC-3 pancreatic cancer cells in mice. These findings suggest that LNP-mediated delivery of miR-634 can potentially be used for cancer therapy.
format Online
Article
Text
id pubmed-6938807
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher American Society of Gene & Cell Therapy
record_format MEDLINE/PubMed
spelling pubmed-69388072020-01-06 Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy Gokita, Kentaro Inoue, Jun Ishihara, Hiroshi Kojima, Kazuyuki Inazawa, Johji Mol Ther Nucleic Acids Article MicroRNAs (miRNAs) are endogenous small noncoding RNAs that negatively regulate gene expression by interfering with the translation or stability of target transcripts. Some tumor-suppressive miRNAs can concurrently target multiple cancer-promoting genes and may be useful as therapeutic anticancer agents. However, the development of drug delivery systems is critical for the implementation of miRNA-based therapeutics. We have previously demonstrated that the enforced expression of miR-634 effectively induces apoptosis by concurrently and directly targeting genes associated with mitochondrial homeostasis, antiapoptosis signaling, antioxidant ability, and autophagy in cancer cells. In the current study, we validated the therapeutic potential of lipid nanoparticle (LNP)-mediated delivery of miR-634 for cancer therapy. We confirmed the ability of enforced expression of miR-634 to induce apoptosis in various cancer cell lines, including pancreatic cancer cells. Intravenous administration of LNPs harboring miR-634 significantly reduced the xenograft tumor growth of BxPC-3 pancreatic cancer cells in mice. These findings suggest that LNP-mediated delivery of miR-634 can potentially be used for cancer therapy. American Society of Gene & Cell Therapy 2019-11-26 /pmc/articles/PMC6938807/ /pubmed/31877409 http://dx.doi.org/10.1016/j.omtn.2019.10.045 Text en © 2019 The Author(s) 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
Gokita, Kentaro
Inoue, Jun
Ishihara, Hiroshi
Kojima, Kazuyuki
Inazawa, Johji
Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy
title Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy
title_full Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy
title_fullStr Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy
title_full_unstemmed Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy
title_short Therapeutic Potential of LNP-Mediated Delivery of miR-634 for Cancer Therapy
title_sort therapeutic potential of lnp-mediated delivery of mir-634 for cancer therapy
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6938807/
https://www.ncbi.nlm.nih.gov/pubmed/31877409
http://dx.doi.org/10.1016/j.omtn.2019.10.045
work_keys_str_mv AT gokitakentaro therapeuticpotentialoflnpmediateddeliveryofmir634forcancertherapy
AT inouejun therapeuticpotentialoflnpmediateddeliveryofmir634forcancertherapy
AT ishiharahiroshi therapeuticpotentialoflnpmediateddeliveryofmir634forcancertherapy
AT kojimakazuyuki therapeuticpotentialoflnpmediateddeliveryofmir634forcancertherapy
AT inazawajohji therapeuticpotentialoflnpmediateddeliveryofmir634forcancertherapy