Titanium(IV) targets phosphoesters on nucleotides: implications for the mechanism of action of the anticancer drug titanocene dichloride

Reactions between the anticancer drug titanocene dichloride (Cp2TiCl2) and various nucleotides and their constituents in aqueous solution or N,N-dimet hylformamide (DMF) have been investigated by H-1 and P-31 NMR spectroscopy and in the solid state by IR spectroscopy. In aqueous solution over the pH* (PH meter reading in D2O) range 2.3-6.5, CMP forms one new species with Ti (IV) bound only to the phosphate group. In acidic media at PH* < 4.6, three species containing titanocene bound to the phosphate group of dGMP, AMP, d TMP and UMP are formed rapidly. The bases also appear to influence titanoce ne binding. Only one of these Ti(IV)-bound species can be detected in the P H* range of 4.6-6.5 in each case. The order of reactivity towards Cp2TiCl2( aq) at PH* ca. 3 is GMP > TMP approximate to AMP > CMP. At PH* > 7.0, hydro lysis of Cp2TiCl2 predominated and little reaction with the nucleotides was observed. Binding of deoxyribose 5'-phosphate and 4-nitrophenyl phosphate to CpTiCl2(aq) via their phosphate groups was detected by P-31 NMR spectros copy, but no reaction between Cp2TiCl2(aq) and deoxyguanosine, 9-ethylguani ne or deoxy-D-ribose was observed in aqueous solution. The nucleoside phosp hodiesters 3',5'-cyclic GMP and 2',3'-cyclic CMP did not react with Cp2TiCl 2(aq) in aqueous solution; however, in the less polar solvent DMF, 3',5'-cy clic GMP coordination to {Cp2Ti}(2+) via its phosphodiester group was readi ly observed. Binding of titanocene to the phosphodiester group of the dinuc leotide GpC was also observed in DMF by P-31 NMR. The nucleoside triphospha tes ATP and GTP reacted more extensively with Cp2TiCl2(aq) than their monop hosphates, complexes with bound phosphate groups were formed in acidic medi a and to a lesser extent at neutral PH. Cleavage of phosphate bonds in ATP (and GTP) by Cp2TiCl2(aq) to form inorganic phosphate, AMP (or GMP) and ADP (or GDP) was observed in aqueous solutions. In addition, titanocene bindin g to ATP was not inhibited by Mg(II), but the ternary complex titanocene-AT P-Mg appeared to form. These reactions contrast markedly with those of the drug cisplatin, which binds predominantly to the base nitrogen atoms of nuc leotides and only weakly to the phosphate groups. The high affinity of Ti(I V) for phosphate groups may be important for its biological activity.