Erba E, Pepe S, Ubezio P, Lorico A, Morasca L, Mangioni C, Landoni F, D'Incalci M
Br J Cancer. 1986 Dec;54(6):925-32. doi: 10.1038/bjc.1986.263.
The growth inhibitory effects, the reduction of [3H]-TdR incorporation and the perturbation of the cell cycle induced by the new agent mitozolomide on the M14 human melanoma cell line and on the SW626 human ovarian cancer cell line were compared to those produced by BCNU. Flow cytometry showed an interesting difference: at the high concentration mitozolomide induced an accumulation of cells in S middle and S late-G2-M phase of the cell cycle whereas BCNU caused only a block in S late-G2-M. Further studies were aimed at investigating the susceptibility of freshly isolated human ovarian cancer cells to pharmacologically reasonable mitozolomide concentrations. Only in one out of 16 primary cultures of human ovarian cancers was mitozolomide able to induce cell cycle perturbation, suggesting that ovarian carcinoma cells may not be sensitive to this drug.
将新型药物米托唑胺对M14人黑色素瘤细胞系和SW626人卵巢癌细胞系的生长抑制作用、[3H]-TdR掺入的减少以及细胞周期的扰动与卡氮芥所产生的作用进行了比较。流式细胞术显示出一个有趣的差异:在高浓度下,米托唑胺诱导细胞在细胞周期的S中期和S后期 - G2 - M期积累,而卡氮芥仅导致S后期 - G2 - M期的阻滞。进一步的研究旨在调查新鲜分离的人卵巢癌细胞对药理学上合理的米托唑胺浓度的敏感性。在16个人卵巢癌原代培养物中,只有1个培养物中的米托唑胺能够诱导细胞周期扰动,这表明卵巢癌细胞可能对这种药物不敏感。