Résumé
Peroxisome proliferator-activated receptor beta (PPAR beta) and Na(V)1.5 voltage-gated sodium channels have independently been shown to regulate human breast cancer cell invasiveness. The n-3 polyunsaturated docosahexaenoic acid (DHA, 22:6n-3), a natural ligand of PPAR, is effective in increasing survival and chemotherapy efficacy in breast cancer patient with metastasis. DHA reduces breast cancer cell invasiveness and it also inhibits PPAR beta expression. We have shown previously that Na(V)1.5 promotes MDA-MB-231 breast cancer cells invasiveness by potentiating the activity of Na+/H+ exchanger type 1 (NHE-1), the major regulator of H+ efflux in these cells. We report here that DHA inhibited Na(V)1.5 current and NHE-1 activity in human breast cancer cells, and in turn reduced Na(V)1.5-dependent cancer cell invasiveness. For the first time, we show that antagonizing PPAR beta, or inhibiting its expression, reduced Na(V)1.5 mRNA and protein expression and Na(V)1.5 current, as well as NHE-1 activity and cell invasiveness. Consistent with these results, the DHA-induced reduction of both Na(V)1.5 expression and NHE-1 activity was abolished in cancer cells knocked-down for the expression of PPAR beta (shPPAR beta). This demonstrates a direct link between the inhibition of PPAR beta expression and the inhibition of Nav1.5/NHE-1 activities and breast cancer cell invasiveness. This study provides new mechanistic data advocating for the use of natural fatty acids such as DHA to block the development of breast cancer metastases.