Author/Authors :
Shah، نويسنده , , Neha and Antony، نويسنده , , Thomas and Haddad، نويسنده , , Salim and Amenta، نويسنده , , Peter and Shirahata، نويسنده , , Akira and Thomas، نويسنده , , T.J. and Thomas، نويسنده , , C.U. Thresia، نويسنده ,
Abstract :
We studied the therapeutic potential of two polyamine analogs on breast cancer using FVB/NTgN (MMTVneu), a transgenic mouse model with neu/erb-B2 oncogene overexpression. Treatment was initiated at 31 weeks of age with bis(ethyl)norspermine (BE333) and its higher homolog, BE3333 as i.p. injections once weekly. There was a 40% reduction in the average number of tumors per mouse in both treatment groups, by 10 weeks of treatment. BE3333-treated mice had 70–75% lower tumor volume than controls. Spermidine/spermine acetyl transferase activity was significantly higher in tumor tissues and kidneys of treated animals, whereas polyamine levels were lower than controls. Beneficial effects were also evident from the mortality rates in control and treatment groups. Our results suggest a potential use of selected bis(ethyl) polyamine analogs as antitumor agents in breast cancer.