Cohen D, Steel G G
Br J Cancer. 1972 Oct;26(5):413-9. doi: 10.1038/bjc.1972.54.
The cell population kinetics of the transmissible venereal tumour of the dog was studied at two different stages of tumour growth using the labelled mitoses technique. At the first stage the tumours were growing with a doubling time of about 4 days; at the second stage their growth rate was limited, probably by an immune reaction on the part of the host, to a doubling time greater than 20 days.Labelling of the tumour cells was found to be extremely heterogeneous throughout the tumour. Mitotic figures, however, were present in well labelled as well as in poorly labelled fields, suggesting that thymidine did not reach all regions of the tumour nodules. The data were therefore analysed assuming that the cells in well labelled areas were representative of the total cell population in the neoplasm. The timing of the cell cycle was found to be similar in the rapidly growing tumours and in those growing more slowly. It is concluded that the slowing of growth was due to a considerable increase in the rate of cell loss as a result of the immune reaction.
利用标记有丝分裂技术,在肿瘤生长的两个不同阶段研究了犬传染性性病肿瘤的细胞群体动力学。在第一阶段,肿瘤以约4天的倍增时间生长;在第二阶段,其生长速率受到限制,可能是由于宿主的免疫反应,倍增时间大于20天。发现肿瘤细胞的标记在整个肿瘤中极其不均一。然而,有丝分裂象在标记良好和标记较差的区域均有出现,这表明胸腺嘧啶核苷并未到达肿瘤结节的所有区域。因此,在分析数据时假设标记良好区域的细胞代表肿瘤中总的细胞群体。结果发现,快速生长的肿瘤和生长较慢的肿瘤中细胞周期的时间相似。得出的结论是,生长减慢是由于免疫反应导致细胞丢失率显著增加所致。