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Nitro-fatty acids (NFAs) are endogenous lipid mediators capable of post-translational modifications of selected regulatory proteins. Here, we investigated the anti-cancerous effects of nitro-oleic acid (NO 2 OA) and its combination with gamma irradiation on different cancer cell lines. The effects of NO 2 OA on cell death, cell cycle distribution, or expression of p21 and cyclin D1 proteins were analyzed in cancer (A-549, HT-29 and FaDu) or normal cell lines (HGF, HFF-1). Dose enhancement ratio at 50 % survival fraction (DER IC50 ) was calculated for samples pre-treated with NO 2 OA followed by gamma irradiation. NO 2 OA suppressed viability and induced apoptotic cell death. These effects were cell line specific but not in general selective for cancer cells. HT-29 cell line exerted higher sensitivity toward NO 2 OA treatment among cancer cell lines tested: induction of cell cycle arrest in the G2/M phase was associated with an increase in p21 and a decrease in cyclin D1 expression. Pre-treatment of HT-29 cells with NO 2 OA prior irradiation showed a significantly increased DER IC50 , demonstrating radiosensitizing effects. In conclusion, NO 2 OA exhibited potential for combined chemoradiotherapy. Our results encourage the development of new NFAs with improved features for cancer chemoradiation.

Cell-type specific anti-cancerous effects of nitro-oleic acid and its combination with gamma irradiation