Courtenay V D
Br J Cancer. 1976 Jul;34(1):39-45. doi: 10.1038/bjc.1976.119.
A soft agar colony assay has been developed for the B16 mouse melanoma and the Lewis lung tumour. The special features of the technique are the use of a gas phase with 5% O2 instead of air and the addition of rat red blood cells. Single cell suspensions are prepared by trypsinization from the solid tumour and the cells are plated out in 0-3% agar over a layer of 0-5% agar in 30-mm Petri dishes. After 8 to 15 days' incubation in 5% O2, colonies of more than 50 cells are produced. Plating efficiencies of between 30 and 50% are usually obtained. The addition of up to 10(4) heavily irradiated tumour cells gives some further improvement in plating efficiency for the B16 melanoma but not for the Lewis lung tumour. Applications of the technique to measure cell survival in the two tumours after treatment with cytotoxic drugs and radiation are reported. The scatter of experimental points is relatively small, and in comparative experiments good agreement has been obtained with results using in vivo assay techniques.
已针对B16小鼠黑色素瘤和Lewis肺癌开发了软琼脂集落测定法。该技术的特点是使用含5%氧气的气相而非空气,并添加大鼠红细胞。通过胰蛋白酶消化从实体瘤制备单细胞悬液,然后将细胞接种于30毫米培养皿中0-5%琼脂层上的0-3%琼脂中。在5%氧气中孵育8至15天后,可产生超过50个细胞的集落。通常获得的接种效率在30%至50%之间。添加多达10(4)个经大量辐照的肿瘤细胞可使B16黑色素瘤的接种效率进一步提高,但对Lewis肺癌无效。报告了该技术在测量细胞毒性药物和辐射处理后两种肿瘤细胞存活率方面的应用。实验点的离散度相对较小,在比较实验中,与体内测定技术的结果取得了良好的一致性。