Huang Chih-Yu, Huang Hsuan-Yu, Forrest Michael D, Pan Yun-Ru, Wu Wei-Jen, Chen Hueih-Min
Nano Biomedical Group, National Nano Device Laboratories, National Applied Research Laboratories, Hsinchu, Taiwan.
Department of Computer Science, University of Warwick, Coventry, United Kingdom.
PLoS One. 2014 Oct 13;9(10):e109174. doi: 10.1371/journal.pone.0109174. eCollection 2014.
Cecropin B is a natural antimicrobial peptide and CB1a is a custom, engineered modification of it. In vitro, CB1a can kill lung cancer cells at concentrations that do not kill normal lung cells. Furthermore, in vitro, CB1a can disrupt cancer cells from adhering together to form tumor-like spheroids. Mice were xenografted with human lung cancer cells; CB1a could significantly inhibit the growth of tumors in this in vivo model. Docetaxel is a drug in present clinical use against lung cancers; it can have serious side effects because its toxicity is not sufficiently limited to cancer cells. In our studies in mice: CB1a is more toxic to cancer cells than docetaxel, but dramatically less toxic to healthy cells.
天蚕素B是一种天然抗菌肽,而CB1a是对其进行的定制化工程改造。在体外,CB1a能够在不杀死正常肺细胞的浓度下杀死肺癌细胞。此外,在体外,CB1a能够破坏癌细胞之间的黏附,使其无法形成肿瘤样球体。将人肺癌细胞异种移植到小鼠体内;在这个体内模型中,CB1a能够显著抑制肿瘤生长。多西他赛是目前临床上用于治疗肺癌的一种药物;它会产生严重的副作用,因为其毒性对癌细胞的限制不够充分。在我们对小鼠的研究中:CB1a对癌细胞的毒性比多西他赛更强,但对健康细胞的毒性则显著更低。