Henss H, Fiebig H H, Meinhardt K, Löhr G W
J Cancer Res Clin Oncol. 1984;108(2):233-5. doi: 10.1007/BF00402473.
Human tumors growing as nude mice xenografts were investigated for growth in a clonogenic assay. Colony formation of more than 30 colonies per plate was obtained in 47 of 63 tumors examined (74.6%). The growth rate was enhanced by raising the concentration of fetal calf serum in the culture medium. Plating efficiency ranged from 0.0003% to 5.5%. To study the applicability of this model for screening new anticancer drugs, preliminary studies in drug sensitivity were conducted with continuous incubation of different anticancer drugs in a dose range of 1/10 to 10 times the maximum achievable plasma level. The highest concentration almost always led to a complete suppression of colony growth. In our opinion the procedure described may be a useful combination of two methods in predictive drug testing, provided drug concentration and mode of drug incubation are adequately considered.
对以裸鼠异种移植瘤形式生长的人类肿瘤进行了克隆形成试验以研究其生长情况。在所检测的63个肿瘤中,有47个(74.6%)每平板形成了超过30个集落。通过提高培养基中胎牛血清的浓度可提高生长速率。接种效率范围为0.0003%至5.5%。为了研究该模型在筛选新型抗癌药物方面的适用性,在1/10至最大可达到血浆水平10倍的剂量范围内,对不同抗癌药物进行连续孵育,开展了药物敏感性的初步研究。最高浓度几乎总是导致集落生长完全受到抑制。我们认为,只要充分考虑药物浓度和药物孵育方式,所描述的程序可能是预测性药物测试中两种方法的有用结合。