Kasagi T, Tazawa K, Yamashita I, Ishizawa S, Masuyama K, Fujimaki M, Maeda M
2nd Department of Surgery, Toyama Medical and Pharmaceutical University.
Nihon Gan Chiryo Gakkai Shi. 1990 Jan 20;25(1):112-20.
For prophylactic therapy to inhibit hepatic metastatic recurrence after surgical treatment of gastro-intestinal carcinomas, the effects of OK-432, a biological response modifier (BRM), were examined with inoculation of tumor cells and administration of OK-432 via portal vein. Experiments with the inhibition of liver metastasis were performed as follows. The animals were divided into five groups. Group 1: 1.0 KE of OK-432 was given intraportally 5 minutes after injection of 5.0 X 10(6) tumor cells per rat via the portal vein. Group 2: Non-medicated group, only 5.0 X 10(6) tumor cells per rat were injected into portal vein, as the control for group 1. Group 3: 0.5 KE of OK-432 and 2.5 X 10(6) tumor cells per rat were used. Group 4: 1.0 KE of OK-432 and 2.5 X 10(6) tumor cells were used. Group 5: Non-medicated group, injected with 2.5 X 10(6) tumor cells as the control group for groups 3 and 4. Colonies of metastases in the liver of each group were examined by autopsy on the 30th day after treatment. Metastases were observed in 75% of group 1, 100% of group 2, 58.8% of group 3, 64.3% of group 4 and in 90% of group 5. For the investigation of the mechanisms to inhibit these liver metastases, 51Cr labeled AH60C tumor cells were injected into the portal vein, and the remained of radioactivity in rat liver was examined. The result showed that OK-432 injected into the portal vein did not directly kill the lodging tumor cells. To prove the morphological evidence of inhibition of hepatic metastasis, the changes of tumor cells were microscopically observed.(ABSTRACT TRUNCATED AT 250 WORDS)
为了研究预防性治疗对胃肠道癌手术后肝转移复发的抑制作用,通过门静脉接种肿瘤细胞并给予生物反应调节剂(BRM)OK-432,观察其效果。进行肝转移抑制实验如下。将动物分为五组。第1组:经门静脉给每只大鼠注射5.0×10(6)个肿瘤细胞5分钟后,经门静脉给予1.0KE的OK-432。第2组:非用药组,仅经门静脉给每只大鼠注射5.0×10(6)个肿瘤细胞,作为第1组的对照。第3组:使用0.5KE的OK-432和每只大鼠2.5×10(6)个肿瘤细胞。第4组:使用1.0KE的OK-432和2.5×10(6)个肿瘤细胞。第5组:非用药组,注射2.5×10(6)个肿瘤细胞,作为第3组和第4组的对照组。治疗后第30天通过尸检检查每组肝脏中的转移瘤菌落。第1组中75%观察到转移,第2组为100%,第3组为58.8%,第4组为64.3%,第5组为90%。为了研究抑制这些肝转移的机制,将51Cr标记的AH60C肿瘤细胞注入门静脉,并检测大鼠肝脏中的放射性残留。结果表明,经门静脉注射的OK-432不会直接杀死着床的肿瘤细胞。为了证明抑制肝转移的形态学证据,在显微镜下观察肿瘤细胞的变化。(摘要截短于250字)