Schultze B, Jellinghaus W, Basler U, Dettmer J, Maurer W
J Cancer Res Clin Oncol. 1983;105(3):266-74. doi: 10.1007/BF00395756.
Cell kinetic studies on the effect of vincristine (VCR) on cells in different cell-cycle phases were carried out using single- and double-labeling methods with 3H- and 14C-thymidine. Studies on mouse L 1210 and JB-1 ascites tumor cells, mouse jejunal crypt cells as well as on HeLa cells have shown that VCR affects cells not only during or prior to mitosis, but also cells that are in S phase at the time of VCR application. These cells are arrested during the next mitosis. Cells arrested in mitosis even with small doses of VCR subsequently become necrotic. Thus, it has been shown experimentally that an in vivo synchronization of tumor cells cannot be achieved with VCR and, therefore, the effect of a so-called synchronization therapy with VCR is not due to synchronization of tumor cells.
采用³H-胸腺嘧啶核苷和¹⁴C-胸腺嘧啶核苷单标记及双标记法,对长春新碱(VCR)对不同细胞周期阶段细胞的作用进行了细胞动力学研究。对小鼠L1210和JB-1腹水瘤细胞、小鼠空肠隐窝细胞以及HeLa细胞的研究表明,VCR不仅在有丝分裂期间或之前影响细胞,而且在应用VCR时处于S期的细胞也会受到影响。这些细胞在下一次有丝分裂期间被阻滞。即使使用小剂量的VCR,阻滞在有丝分裂期的细胞随后也会坏死。因此,实验表明,VCR不能在体内使肿瘤细胞同步化,所以,所谓的VCR同步化疗法的效果并非源于肿瘤细胞的同步化。