Cytotoxic Effects of 5-Azacytidine on Primary Tumour Cells and Cancer Stem Cells from Oral Squamous Cell Carcinoma: An In Vitro FTIRM Analysis.
Valentina NotarstefanoAlessia BelloniSimona SabbatiniChiara ProGiulia OrilisiRiccardo MonterubbianesiVincenzo ToscoHugh J ByrneLisa VaccariElisabetta GiorginiPublished in: Cells (2021)
In the present study, the cytotoxic effects of 5-azacytidine on primary Oral Squamous Cell Carcinoma cells (OSCCs) from human biopsies, and on Cancer Stem Cells (CSCs) from the same samples, were investigated by an in vitro Fourier Transform InfraRed Microscospectroscopy (FTIRM) approach coupled with multivariate analysis. OSCC is an aggressive tumoral lesion of the epithelium, accounting for ~90% of all oral cancers. It is usually diagnosed in advanced stages, and this causes a poor prognosis with low success rates of surgical, as well as radiation and chemotherapy treatments. OSCC is frequently characterised by recurrence after chemotherapy and by the development of a refractoriness to some employed drugs, which is probably ascribable to the presence of CSCs niches, responsible for cancer growth, chemoresistance and metastasis. The spectral information from FTIRM was correlated with the outcomes of cytotoxicity tests and image-based cytometry, and specific spectral signatures attributable to 5-azacytidine treatment were identified, allowing us to hypothesise the demethylation of DNA and, hence, an increase in the transcriptional activity, together with a conformational transition of DNA, and a triggering of cell death by an apoptosis mechanism. Moreover, a different mechanism of action between OSSC and CSC cells was highlighted, probably due to possible differences between OSCCs and CSCs response.
Keyphrases
- cancer stem cells
- squamous cell
- cell cycle arrest
- cell death
- poor prognosis
- induced apoptosis
- papillary thyroid
- single molecule
- pi k akt
- endoplasmic reticulum stress
- endothelial cells
- optical coherence tomography
- circulating tumor
- long non coding rna
- gene expression
- locally advanced
- oxidative stress
- transcription factor
- cell free
- squamous cell carcinoma
- healthcare
- signaling pathway
- type diabetes
- magnetic resonance imaging
- radiation therapy
- young adults
- molecular dynamics simulations
- adipose tissue
- childhood cancer
- metabolic syndrome
- machine learning
- molecular dynamics
- single cell
- high resolution
- skeletal muscle
- induced pluripotent stem cells
- atomic force microscopy
- replacement therapy
- drug induced