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Therapeutic efficacy of modified anti-miR21 in metastatic prostate cancer.
- Source :
-
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 2020 Aug 27; Vol. 529 (3), pp. 707-713. Date of Electronic Publication: 2020 Jul 18. - Publication Year :
- 2020
-
Abstract
- Despite improved therapeutic efficacy of the locked nucleic acid (LNA)- and peptide nucleic acid (PNA)-modified antisense microRNAs (anti-miRs), their wider application in clinical practice is still not thoroughly investigated. This study aimed to investigate the stability and therapeutic efficacy of the modified LNA- and PNA-type anti-miRs in a murine prostate cancer model under various treatment conditions. After verifying the anti-cancer potential of anti-miR21 by targeting tumor suppressor PTEN, the potential of the modified LNA- and PNA-type anti-miR21s was compared in vitro and in vivo. We found that PNA-type anti-miR21 showed better stability and therapeutic efficacy in the xenografted mouse tumor model than the LNA-type anti-miR21. Furthermore, PNA-type anti-miR21 treatment showed reduced tumor metastasis. This study may serve as a ground for exploring diverse choices in therapeutic oligonucleotide modification techniques to improve cancer treatment.<br /> (Copyright © 2020 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Antagomirs genetics
Cell Line, Tumor
Genetic Therapy
Humans
Male
Mice
Mice, Inbred BALB C
Mice, Nude
Neoplasm Metastasis genetics
Neoplasm Metastasis therapy
Oligonucleotides genetics
PC-3 Cells
Peptide Nucleic Acids genetics
Prostatic Neoplasms genetics
Antagomirs therapeutic use
MicroRNAs genetics
Oligonucleotides therapeutic use
Peptide Nucleic Acids therapeutic use
Prostatic Neoplasms therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1090-2104
- Volume :
- 529
- Issue :
- 3
- Database :
- MEDLINE
- Journal :
- Biochemical and biophysical research communications
- Publication Type :
- Academic Journal
- Accession number :
- 32736696
- Full Text :
- https://doi.org/10.1016/j.bbrc.2020.05.215