Winder D, Günzburg W H, Erfle V, Salmons B
Bavarian Nordic Research Institute, Munich, Germany.
Biochem Biophys Res Commun. 1998 Jan 26;242(3):608-12. doi: 10.1006/bbrc.1997.8014.
The antimicrobial peptides cecropin and melittin are known to exhibit antitumour activity in tumour derived cell lines. To achieve a similar effect in vivo these peptides would have to be given repeatedly to maintain therapeutic levels, which may be pharmacologically unfavourable. The expression of the genes encoding such antimicrobial peptides in the desired cell type may circumvent these problems. Expression constructs carrying cecropin or melittin have been introduced into a human bladder carcinoma derived cell line and the resultant cell clones analysed for tumorigenicity in nude mice. Expression of cecropin resulted in either a complete loss of tumorigenicity in some clones or reduced tumorigenicity, as measured by latency of tumour formation. These results suggest that vector mediated delivery of this gene to tumour cells may prove useful for cancer gene therapy.
已知抗菌肽天蚕素和蜂毒肽在肿瘤衍生细胞系中具有抗肿瘤活性。为了在体内达到类似效果,这些肽必须反复给药以维持治疗水平,这在药理学上可能不利。在所需细胞类型中编码此类抗菌肽的基因表达可能会规避这些问题。携带天蚕素或蜂毒肽的表达构建体已被引入人膀胱癌衍生细胞系,并对所得细胞克隆进行裸鼠致瘤性分析。天蚕素的表达导致一些克隆的致瘤性完全丧失,或如通过肿瘤形成潜伏期所测,致瘤性降低。这些结果表明,载体介导的该基因向肿瘤细胞的递送可能对癌症基因治疗有用。