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Protein arginine (N)-methyl transferase 7 (PRMT7) as a potential target for the sensitization of tumor cells to camptothecins
Authors:Verbiest Vincent  Montaudon Danièle  Tautu Michel T  Moukarzel Joyce  Portail Jean-Pierre  Markovits Judith  Robert Jacques  Ichas François  Pourquier Philippe
Affiliation:INSERM U916, VINCO, Institut Bergonié and Université Victor Segalen Bordeaux 2, 33076 Bordeaux, France.
Abstract:PRMT7 belongs to the protein arginine methyl-transferases family. We show that downregulation of PRMT7alpha and beta isoforms in DC-3F hamster cells was associated with increased sensitivity to the Top1 inhibitor camptothecin (CPT). This effect was not due to a change in Top1 contents or catalytic activity, or to a difference in the reversal of DNA breaks. Overexpression of PRMT7alpha and beta in DC-3F cells had no effect on CPT sensitivity, whereas it conferred a resistance to DC-3F/9-OH-E cells for which both isoforms are reduced by two- to three-fold as compared to DC-3F parental cells. Finally, downregulation of the human PRMT7 could also sensitize HeLa cells to CPT, suggesting that it could be used as a target to potentiate CPT derivatives.
Keywords:Protein arginine-methyl transferase (PRMT)   Topoisomerase I   Camptothecin   Apoptosis   Drug response   Resistance
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