COMPARISON OF CELL-CYCLE PHASE PERTURBATIONS INDUCED BY THE DNA-MINOR-GROOVE ALKYLATOR TALLIMUSTINE AND BY MELPHALAN IN THE SW626 CELL-LINE

Tallimustine or N-deformyl-N-[4-N-N,N-bis(2-chloroethylamino)benzoyl], a distamycin-A derivative (FCE 245 17), is a novel anti-cancer agent which alkylates N3 adenine in the minor groove of DNA. The cell-cycle phase perturbations induced by the drug were investigated and compared with those caused by melphalan (L-PAM) in SW626 human ovarian-cancer cells. By coupling bromodeoxyuridine (BUdR) immunoreaction with biparametric flow-cytometric (FCM) analysis, we investigated the cell-cycle phase perturbation induced by tallimustine or L-PAM, considering separately the cells which, during the 1-hr treatment, were in the S phase or in G(1)-G(2)/M phases of the cell cycle. L-PAM delayed the S-phase progression of cells exposed to the drug when they were in S phase, with a cansequent accumulation of cells as soon as they reached the G(2) phase. In contrast, the S-phase cells treated with tallimustine were not perturbed during the DNA-synthesis phase progression, and were blocked in G(2) only after they had passed through the G(1)/S transition of a new cell cycle. In cells which were in G(1) or G(2)/M phases during drug treatment, tallimustine and L-PAM caused similar accumulation in G(2). The differences in the cell-cycle perturbation caused by tallimustine and L-PAM may well be related to the different DNA damage the 2 drugs produced. These findings emphasize the different properties of DNA-minor-groove alkylating agents and conventional ones. (C) 1995 Wiley-Liss, Inc.