Van de Vrie W, Marquet R L, Eggermont A M
Department of Surgical Oncology, Rotterdam Cancer Institute, The Netherlands.
J Cancer Res Clin Oncol. 1997;123(1):21-4. doi: 10.1007/BF01212610.
The immunosuppressive drug cyclosporin A has been evaluated recently in phase II trials in cancer therapy as a reverter of P-glycoprotein-mediated multidrug resistance. As an immunosuppressive agent, cyclosporin A potentially can enhance tumour growth. We investigated this potency of cyclosporin A in the weakly immunogenic CC531 colon adenocarcinoma model, using the same dose that had previously been shown to intensify the antitumour activity of doxorubicin in vivo. In vitro cyclosporin A caused no growth acceleration and only in high doses was growth inhibition of CC531 cells observed. In vivo no evidence of growth enhancement was found in short-term assays but, after 4 weeks, rats treated with cyclosporin A had a significantly higher tumour load, mainly consisting of locoregional metastases. These experiments in the CC531 tumour model show that cyclosporin A, used as a reverter of multidrug resistance, may produce short-term improvement of antitumour activity but may also induce enhancement of tumour metastasis.
免疫抑制药物环孢素A最近在癌症治疗的II期试验中作为P-糖蛋白介导的多药耐药逆转剂进行了评估。作为一种免疫抑制剂,环孢素A有可能促进肿瘤生长。我们在弱免疫原性的CC531结肠腺癌模型中研究了环孢素A的这种作用,使用的剂量与之前在体内增强阿霉素抗肿瘤活性的剂量相同。在体外,环孢素A不会导致生长加速,只有在高剂量时才观察到对CC531细胞的生长抑制。在体内,短期试验中未发现生长增强的证据,但4周后,用环孢素A治疗的大鼠肿瘤负荷明显更高,主要由局部区域转移组成。在CC531肿瘤模型中的这些实验表明,用作多药耐药逆转剂的环孢素A可能会在短期内改善抗肿瘤活性,但也可能诱导肿瘤转移增强。