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6BIO Enhances Oligonucleotide Activity in Cells: A Potential Combinatorial Anti-androgen Receptor Therapy in Prostate Cancer Cells
- Source :
- Molecular Therapy. 25:79-91
- Publication Year :
- 2017
- Publisher :
- Elsevier BV, 2017.
-
Abstract
- Approximately 15%–25% of men diagnosed with prostate cancer do not survive their disease. The American Cancer Society estimated that for the year 2016 the number of prostate cancer deaths will be 26,120. Thus, there is a critical need for novel approaches to treat this deadly disease. Using high-throughput small-molecule screening, we found that the small molecule 6-bromo-indirubin-3′-oxime (6BIO) significantly improves the targeting of antisense oligonucleotides (ASOs) delivered by gymnosis (i.e., in the absence of any transfection reagents) in both the cell cytoplasm and the nucleus. Furthermore, as a single agent, 6BIO had the unexpected ability to simultaneously downregulate androgen receptor (AR) expression and AR signaling in prostate cancer cells. This includes downregulating levels of the AR-V7, a drug-resistance-related AR splice variant that is important in the progression of prostate cancer. Combining 6BIO and an anti-AR oligonucleotide (AR-ASO) can augment the downregulation of AR expression. We also demonstrated that 6BIO enhances ASO function and represses AR expression through the inhibition of the two main glycogen synthase kinase 3 (GSK-3) isoforms: GSK-3α and GSK-3β activity. Our findings provide a rationale for the use of 6BIO as a single agent or as part of a combinatorial ASO-based therapy in the treatment of human prostate cancer.
- Subjects :
- Male
0301 basic medicine
Cytoplasm
Indoles
RNA Splicing
Oligonucleotides
Anti-Androgen
Antineoplastic Agents
Biology
Glycogen Synthase Kinase 3
03 medical and health sciences
Prostate cancer
Downregulation and upregulation
GSK-3
Cell Line, Tumor
Oximes
Drug Discovery
Androgen Receptor Antagonists
Genetics
medicine
Humans
Receptor
Molecular Biology
Pharmacology
Glycogen Synthase Kinase 3 beta
Prostatic Neoplasms
Cancer
Drug Synergism
Oncogenes
Transfection
medicine.disease
Molecular biology
Androgen receptor
MicroRNAs
030104 developmental biology
Receptors, Androgen
Cancer research
Molecular Medicine
Original Article
Signal Transduction
Subjects
Details
- ISSN :
- 15250016
- Volume :
- 25
- Database :
- OpenAIRE
- Journal :
- Molecular Therapy
- Accession number :
- edsair.doi.dedup.....36525e9aebe56f0f128baf039dd0056c
- Full Text :
- https://doi.org/10.1016/j.ymthe.2016.10.017