Doxorubicin and Cisplatin Modulate miR-21, miR-106, miR-126, miR-155 and miR-199 Levels in MCF7, MDA-MB-231 and SK-BR-3 Cells That Makes Them Potential Elements of the DNA-Damaging Drug Treatment Response Monitoring in Breast Cancer Cells-A Preliminary Study.
Anna MizielskaIga DziechciowskaRadosław SzczepańskiMałgorzata CisekMałgorzata DąbrowskaJan ŚlężakIzabela KosmalskaMarta RymarczykKlaudia WilkowskaBarbara JacczakEwa TotońNatalia LisiakPrzemysław KopczyńskiBłażej RubiśPublished in: Genes (2023)
One of the most innovative medical trends is personalized therapy, based on simple and reproducible methods that detect unique features of cancer cells. One of the good prognostic and diagnostic markers may be the miRNA family. Our work aimed to evaluate changes in selected miRNA levels in various breast cancer cell lines (MCF7, MDA-MB-231, SK-BR-3) treated with doxorubicin or cisplatin. The selection was based on literature data regarding the most commonly altered miRNAs in breast cancer (21-3p, 21-5p, 106a-5p, 126-3p, 126-5p, 155-3p, 155-5p, 199b-3p, 199b-5p, 335-3p, 335-5p). qPCR assessment revealed significant differences in the basal levels of some miRNAs in respective cell lines, with the most striking difference in miR-106a-5p, miR-335-5p and miR-335-3p-all of them were lowest in MCF7, while miR-153p was not detected in SK-BR-3. Additionally, different alterations of selected miRNAs were observed depending on the cell line and the drug. However, regardless of these variables, 21-3p/-5p, 106a, 126-3p, 155-3p and 199b-3p miRNAs were shown to respond either to doxorubicin or to cisplatin treatment. These miRNAs seem to be good candidates for markers of breast cancer cell response to doxorubicin or cisplatin. Especially since some earlier reports suggested their role in affecting pathways and expression of genes associated with the DNA-damage response. However, it must be emphasized that the preliminary study shows effects that may be highly related to the applied drug itself and its concentration. Thus, further examination, including human samples, is required.
Keyphrases
- breast cancer cells
- cell proliferation
- long non coding rna
- long noncoding rna
- poor prognosis
- drug delivery
- dna damage response
- cancer therapy
- adverse drug
- healthcare
- induced apoptosis
- endothelial cells
- cell cycle arrest
- risk assessment
- stem cells
- single cell
- cell death
- emergency department
- electronic health record
- dna repair
- machine learning
- replacement therapy
- circulating tumor
- smoking cessation
- signaling pathway
- cell therapy
- single molecule