The State Key Laboratory of Pharmaceutical Biotechnology, College of Life Sciences and School of Stomatology, Affiliated Stomatological Hospital, Nanjing University, Nanjing, 210093, P.R. China.
Changzhou High-Tech Research Institute of Nanjing University and Jiangsu TargetPharma Laboratories Inc., Changzhou, 213164, P.R. China.
Sci Rep. 2013 Dec 20;3:3565. doi: 10.1038/srep03565.
The tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a promising cancer therapeutic agent, which kills cancer cells selectively, while leaving normal cells unharmed. However, the emerging resistance of tumor cells and patients to TRAIL-induced apoptosis limits its further application. In this study, we developed a chimeric protein Annexin V-TRAIL (designated as TP8) with higher efficacy than TRAIL both in vitro and in vivo. In vitro, the EC50 of TP8 on a series of tumor cells was much lower than wild-type TRAIL. Annexin V provided this recombinant protein with higher efficacy, while leaving tumor specificity of TRAIL unchanged since TP8 had no effects on normal cells. In vivo, TP8 effectively suppressed tumor growth and prolonged tumor doubling time and tumor growth delay time in mouse xenografts involving multiple cancer cell types including A549, Colo205 and Bel7402. This study provides a new rational strategy to treat TRAIL-resistant cancers.
肿瘤坏死因子相关凋亡诱导配体(TRAIL)是一种很有前途的癌症治疗药物,它能选择性地杀死癌细胞,而不伤害正常细胞。然而,肿瘤细胞和患者对 TRAIL 诱导的细胞凋亡的耐药性的出现限制了它的进一步应用。在这项研究中,我们开发了一种嵌合蛋白 Annexin V-TRAIL(命名为 TP8),它在体外和体内的效果都比 TRAIL 高。在体外,一系列肿瘤细胞的 EC50 比野生型 TRAIL 低得多。Annexin V 使这种重组蛋白具有更高的疗效,同时保持了 TRAIL 的肿瘤特异性不变,因为 TP8 对正常细胞没有影响。在体内,TP8 有效地抑制了包括 A549、Colo205 和 Bel7402 在内的多种癌细胞类型的小鼠异种移植中的肿瘤生长,并延长了肿瘤倍增时间和肿瘤生长延迟时间。这项研究为治疗 TRAIL 耐药性癌症提供了一种新的合理策略。