Effects of photodeoxygenation on cell biology using dibenzothiophene S-oxide derivatives as O(3P)-precursors.
Ankita IsorAustin T O'DeaScott F GradyJohn T PetroffKristin N SkubicBashar AzizChristopher K ArnattRyan D McCullaPublished in: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology (2021)
Photodeoxygenation of dibenzothiophene S-oxide and its derivatives have been used to generate atomic oxygen [O(3P)] to examine its effect on proteins, nucleic acids, and lipids. The unique reactivity and selectivity of O(3P) have shown distinct oxidation products and outcomes in biomolecules and cell-based studies. To understand the scope of its global impact on the cell, we treated MDA-MB-231 cells with 2,8-diacetoxymethyldibenzothiophene S-oxide and UV-A light to produce O(3P) without targeting a specific cell organelle. Cellular responses to O(3P)-release were analyzed using cell viability and cell cycle phase determination assays. Cell death was observed when cells were treated with higher concentrations of sulfoxides and UV-A light. However, significant differences in cell cycle phases due to UV-A irradiation of the sulfoxide were not observed. We further performed RNA-Seq analysis to study the underlying biological processes at play, and while UV-irradiation itself influenced gene expression, there were 9 upregulated and 8 downregulated genes that could be attributed to photodeoxygenation.
Keyphrases
- cell cycle
- single cell
- rna seq
- gene expression
- cell therapy
- cell death
- cell cycle arrest
- cell proliferation
- induced apoptosis
- stem cells
- high throughput
- radiation therapy
- metabolic syndrome
- dna methylation
- drug delivery
- endoplasmic reticulum stress
- genome wide
- insulin resistance
- pi k akt
- signaling pathway
- tandem mass spectrometry