Citation

  • Authors: Germano, A., Rapa, I., Volante, M., De Francia, S., Migliore, C., Berruti, A., Papotti, M., Terzolo, M.
  • Year: 2015
  • Journal: Mol Cell Endocrinol 401 105-10
  • Applications: in vitro / siRNA / INTERFERin
  • Cell type: SW-13

Method

Reverse transfection using 50 nM siRNA. Both siRNA and INTERFERin were diluted in medium without serum, and incubated for 10 minutes at room temperature. Lipoplexes were then transferred to multiwell tissue culture plates and overlaid with 25 Ă— 10^4 cells per well. After 24 hours, the medium was changed.

Abstract

The anti-proliferative activity of mitotane (o,p'DDD) in adrenocortical cancer is mediated by its metabolites o,p'DDE and o,p'DDA. We previously demonstrated a functional link between ribonucleotide reductase M1(RRM1) expression and o,p'DDD activity, but the mechanism is unknown. In this study we assessed the impact of RRM1 on the bioavailability and cytotoxic activity of o,p'DDD, o,p'DDE and o,p'DDA in SW13 and H295R cells. In H295R cells, mitotane and its metabolites showed a similar cytotoxicity and RRM1 expression was not influenced by any drug. In SW13 cells, o,p'DDA only showed a cytotoxic activity and did not modify RRM1 expression, whereas the lack of sensitivity to o,p'DDE was associated to RRM1 gene up-modulation, as already demonstrated for o,p'DDD. RRM1 silencing in SW13 cells increased the intracellular transformation of mitotane into o,p'DDE and o,p'DDA. These data demonstrate that RRM1 gene interferes with mitotane metabolism in adrenocortical cancer cells, as a possible mechanisms of drug resistance.

Pubmed