Proteomic analysis of the vitamin C effect on the doxorubicin cytotoxicity in the MCF-7 breast cancer cell line
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
PubMed
27620743
DOI
10.1007/s00432-016-2259-4
PII: 10.1007/s00432-016-2259-4
Knihovny.cz E-zdroje
- Klíčová slova
- Cell toxicity, Doxorubicin, Label-free quantification, MCF-7 cell line, Vitamin C,
- MeSH
- antioxidancia farmakologie MeSH
- chemorezistence MeSH
- doxorubicin farmakologie MeSH
- kyselina askorbová farmakologie MeSH
- lidé MeSH
- MFC-7 buňky MeSH
- nádory prsu farmakoterapie metabolismus MeSH
- proliferace buněk MeSH
- proteom metabolismus MeSH
- proteomika MeSH
- protinádorová antibiotika farmakologie MeSH
- screeningové testy protinádorových léčiv MeSH
- synergismus léků MeSH
- Check Tag
- lidé MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- antioxidancia MeSH
- doxorubicin MeSH
- kyselina askorbová MeSH
- proteom MeSH
- protinádorová antibiotika MeSH
PURPOSE: Doxorubicin is an anthracycline drug which inhibits the growth of breast cancer cell lines. However, a major factor limiting its use is a cumulative, dose-dependent cardiotoxicity, resulting in a permanent loss of cardiomyocytes. Vitamin C was found to potentiate the cytotoxic effects of a variety of chemotherapeutic drugs including doxorubicin. The aim of the study was to describe the changes in protein expression and proliferation of the MCF-7 cells induced by the vitamin C applied with doxorubicin. METHODS: Label-free quantitative proteomics and real-time cell analysis methods were used to search for proteome and cell proliferation changes. These changes were induced by the pure DOX and by DOX combined with vitamin C applied on the MCF-7 cell line. RESULTS: From the real-time cell analysis experiments, it is clear that the highest anti-proliferative effect occurs with the addition of 200 µM of vitamin C to 1 µM of doxorubicin. By applying both the label-free protein quantification method and total ion current assay, we found statistically significant changes (p ≤ 0.05) of 26 proteins induced by the addition of vitamin C to doxorubicin on the MCF-7 cell line. These differentially expressed proteins are involved in processes such as structural molecule activity, transcription and translation, immune system process and antioxidant, cellular signalling and transport. CONCLUSION: The detected proteins may be capable of predicting response to DOX therapy. This is a key tool in the treatment of breast cancer, and the combination with vit C seems to be of particular interest due to the fact that it can potentiate anti-proliferative effect of DOX.
Institute of Histology and Embryology Faculty of Medicine University of Ljubljana Ljubljana Slovenia
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