High Boron-loaded DNA-Oligomers as Potential Boron Neutron Capture Therapy and Antisense Oligonucleotide Dual-Action Anticancer Agents

• Published in: Molecules (Basel, Switzerland) Vol. 22; no. 9; p. 1393
• Main Authors: Kaniowski, Damian, Ebenryter-Olbińska, Katarzyna, Sobczak, Milena, Wojtczak, Błażej, Janczak, Sławomir, Leśnikowski, Zbigniew J, Nawrot, Barbara
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 23-08-2017; MDPI
• Subjects: Alkynes; Antineoplastic Agents - chemical synthesis; Antineoplastic Agents - chemistry; Antineoplastic Agents - pharmacology; antisense oligonucleotide; Antisense oligonucleotides; BNCT; Boron; Boron - chemistry; Boron Neutron Capture Therapy; Cancer; Chemical compounds; Chromatography, High Pressure Liquid; Circular Dichroism; Complementary DNA; Conjugation; Copper; Deoxyribonucleic acid; Diagnostic systems; DNA; EGFR; Epidermal growth factor; Epidermal growth factor receptors; Gene therapy; HeLa Cells; Humans; Infrared spectroscopy; Lipophilicity; Low concentrations; metallacarborane; Mitochondria; Molecular Structure; Nuclear capture; Nucleic acids; Oligonucleotides, Antisense - chemical synthesis; Oligonucleotides, Antisense - chemistry; Oligonucleotides, Antisense - pharmacology; Pharmacology; Reactive Oxygen Species - chemistry; Receptor, Epidermal Growth Factor - genetics; ROS; Spectroscopy, Fourier Transform Infrared; BNCT; antisense oligonucleotide; metallacarborane; EGFR; ROS
• ISSN: 1420-3049; 1420-3049
• DOI: 10.3390/molecules22091393

Boron cluster-modified therapeutic nucleic acids with improved properties are of interest in gene therapy and in cancer boron neutron capture therapy (BNCT). High metallacarborane-loaded antisense oligonucleotides (ASOs) targeting epidermal growth factor receptor (EGFR) were synthesized through post-synthetic Cu (I)-assisted "click" conjugation of alkyne-modified DNA-oligonucleotides with a boron cluster alkyl azide component. The obtained oligomers exhibited increased lipophilicity compared to their non-modified precursors, while their binding affinity to complementary DNA and RNA strands was slightly decreased. Multiple metallacarborane residues present in the oligonucleotide chain, each containing 18 B-H groups, enabled the use of IR spectroscopy as a convenient analytical method for these oligomers based on the diagnostic B-H signal at 2400-2650 cm
. The silencing activity of boron cluster-modified ASOs used at higher concentrations was similar to that of unmodified oligonucleotides. The screened ASOs, when used in low concentrations (up to 50 μM), exhibited pro-oxidative properties by inducing ROS production and an increase in mitochondrial activities in HeLa cells. In contrast, when used at higher concentrations, the ASOs exhibited anti-oxidative properties by lowering ROS species levels. In the HeLa cells (tested in the MTT assay) treated (without lipofectamine) or transfected with the screened compounds, the mitochondrial activity remained equal to the control level or only slightly changed (±30%). These findings may be useful in the design of dual-action boron cluster-modified therapeutic nucleic acids with combined antisense and anti-oxidant properties.