Franko A J, Kallman R F, Rapacchietta D, Kelley S D
Br J Cancer Suppl. 1980 Apr;4:69-73.
Two potential artifacts, the reutilization of label released from the gut and the influx into solid tumours of labelled host cells, have been measured by occluding the blood flow to tumours during, and for 30 min after, injection of 125IUdR. Previous work has shown that occluded EMT6 and KHJJ tumours exhibit a substantial increase in label, to 30-40% of the total activity in non-occluded tumours within 4 days post-125IUdR injection. In B16 and RIF-1 tumours the influx of label is minimal. Almost all of this entry of 125IUdR results from the influx of labelled host cells. Significant influx was also demonstrated in Lewis lung and KHT tumours. Minimal changes in the extent of influx of labelled host cells were found following irradiation of EMT6 and RIF-1 tumours with 600 or 1400 rad. These doses also resulted in little or no additional loss of 125IUdR despite the fact that 60 to 95% of the tumour cells were killed. Thus, the lysis of the killed cells must proceed very slowly. The conditions necessary for the use of 125IUdR loss to assess cell killing, as opposed to cell lysis, are reviewed.
通过在注射125IUdR期间及之后30分钟阻断肿瘤的血流,对两种潜在的假象,即从肠道释放的标记物的再利用以及标记的宿主细胞流入实体瘤,进行了测量。先前的研究表明,在注射125IUdR后4天内,被阻断血流的EMT6和KHJJ肿瘤的标记物显著增加,达到未被阻断血流肿瘤总活性的30%-40%。在B16和RIF-1肿瘤中,标记物的流入极少。125IUdR的这种进入几乎全部是由于标记的宿主细胞的流入。在Lewis肺癌和KHT肿瘤中也证实有显著的流入。在用600或1400拉德照射EMT6和RIF-1肿瘤后,发现标记的宿主细胞流入程度的变化极小。尽管60%至95%的肿瘤细胞被杀死,但这些剂量也几乎没有导致125IUdR的额外损失。因此,被杀死细胞的裂解一定进行得非常缓慢。本文综述了利用125IUdR损失来评估细胞杀伤而非细胞裂解所需的条件。