Koop S, MacDonald I C, Luzzi K, Schmidt E E, Morris V L, Grattan M, Khokha R, Chambers A F, Groom A C
Department of Medical Biophysics, University of Western Ontario, London, Canada.
Cancer Res. 1995 Jun 15;55(12):2520-3.
Metastasis is an inefficient process; only a few cancer cells are able to form tumors after being released into the circulation. We studied the fate of cancer cells after injection into the circulation, quantifying their survival and ability to extravasate by 1 day later. B16F10 cells, parental or transfectants overexpressing tissue inhibitor of metalloproteinases 1, were injected i.v. into chorioallantoic membrane of chick embryos and analyzed by intravital videomicroscopy. Cell survival was quantified in two ways: (a) 15-microns microspheres were injected with cancer cells, and proportions of viable cells to microspheres were compared before and after injection; and (b) individual cancer cells were monitored continuously for 0.5-8-h intervals covering the first 24 h. Both methods showed virtually no destruction of cells. Greater than 80% of injected cells survived and extravasated by 24 h, indicating that growth after extravasation is a key stage of metastatic control.
转移是一个低效的过程;只有少数癌细胞在进入循环系统后能够形成肿瘤。我们研究了癌细胞注入循环系统后的命运,通过1天后对其存活情况和外渗能力进行量化。将亲本B16F10细胞或过表达金属蛋白酶组织抑制剂1的转染细胞静脉注射到鸡胚的绒毛尿囊膜中,并通过活体视频显微镜进行分析。细胞存活情况通过两种方式进行量化:(a)将15微米的微球与癌细胞一起注射,比较注射前后活细胞与微球的比例;(b)在最初的24小时内,以0.5 - 8小时的间隔连续监测单个癌细胞。两种方法均显示细胞几乎没有被破坏。超过80%的注入细胞在24小时内存活并外渗,这表明外渗后的生长是转移控制的关键阶段。