Chaplin D J, Durand R E, Stratford I J, Jenkins T C
Int J Radiat Oncol Biol Phys. 1986 Jul;12(7):1091-5. doi: 10.1016/0360-3016(86)90233-6.
RSU-1069 is one of a group of compounds of particular interest in radiobiology, since it combines the nitroimidazole ring with a side chain bearing a monofunctional alkylating agent. This compound has been shown to be a potent radiosensitizer both in vitro and in vivo. Furthermore, it has recently been shown to be an effective hypoxic cell cytotoxin in vitro. Our studies have been carried out using the SCCVII squamous carcinoma implanted subcutaneously in C3H mice, using a technique we recently developed which facilitates isolation of tumor cell subpopulations from known locations relative to the tumor blood supply. The response of the separated tumor subpopulations was assessed using a soft agar clonogenic assay. For radiosensitization studies, RSU-1069 was administered i.p. at 0.5 mumol/g 20 min before irradiation and the tumors excised 20 min after irradiation. For toxicity studies, tumors were excised 16-18 hr after RSU-1069 administration. The results obtained to date clearly demonstrate that RSU-1069 is an efficient hypoxic cell radiosensitizer and cytotoxin in this murine tumor and has little effect on well perfused (i.e., oxic) cells.
RSU - 1069是放射生物学中一类特别受关注的化合物之一,因为它将硝基咪唑环与带有单功能烷基化剂的侧链结合在一起。该化合物已被证明在体外和体内都是一种有效的放射增敏剂。此外,最近还表明它在体外是一种有效的缺氧细胞细胞毒素。我们的研究是使用皮下植入C3H小鼠的SCCVII鳞状癌进行的,采用了我们最近开发的一种技术,该技术有助于从相对于肿瘤血液供应的已知位置分离肿瘤细胞亚群。使用软琼脂克隆形成试验评估分离的肿瘤亚群的反应。对于放射增敏研究,在照射前20分钟腹腔注射0.5 μmol/g的RSU - 1069,并在照射后20分钟切除肿瘤。对于毒性研究,在给予RSU - 1069后16 - 18小时切除肿瘤。迄今为止获得的结果清楚地表明,RSU - 1069在这种小鼠肿瘤中是一种有效的缺氧细胞放射增敏剂和细胞毒素,对灌注良好(即有氧)的细胞几乎没有影响。