Taylor A, Jones O W, Grishaver M A
Cancer Res. 1981 Jan;41(1):192-6.
Cells of the Morris hepatoma 7777 cultured in vitro have elevated levels of cytoplasmic thymidine kinase similar to those found in vivo. The cell-doubling time is slightly less than 24 hr. The addition of 5-fluorouracil to the culture medium (10 micrograms/ml) inhibits cell division, stimulates thymidine kinase production, and results in cell death which increases with time. Treated cells release significantly (p less than or equal to 0.01) more thymidine kinase into the culture medium than do untreated cells, and this effect can also be seen following a 60-min pulsed incubation of the cells with 5-fluorouracil. The total activity of thymidine kinase released is proportional to cell death and to the number of cells originally on the plate. These results suggest the possibility of monitoring tumor response to therapy in vivo by measuring serum levels of thymidine kinase.
体外培养的莫里斯肝癌7777细胞的细胞质胸苷激酶水平升高,与体内发现的水平相似。细胞倍增时间略少于24小时。向培养基中添加5-氟尿嘧啶(10微克/毫升)可抑制细胞分裂,刺激胸苷激酶产生,并导致细胞死亡,且随时间增加。与未处理的细胞相比,处理后的细胞向培养基中释放的胸苷激酶明显更多(p小于或等于0.01),在细胞与5-氟尿嘧啶进行60分钟脉冲孵育后也能观察到这种效应。释放的胸苷激酶的总活性与细胞死亡以及平板上最初的细胞数量成正比。这些结果表明,通过测量血清胸苷激酶水平来监测体内肿瘤对治疗的反应是有可能的。