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Annexin V-TRAIL fusion protein is a more sensitive and potent apoptotic inducer for cancer therapy

机译:Annexin V-TRAIL融合蛋白是用于癌症治疗的更敏感和有效的凋亡诱导剂

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摘要

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.
机译:肿瘤坏死因子相关的凋亡诱导配体(TRAIL)是一种有前途的癌症治疗剂,可以选择性杀死癌细胞,而正常细胞则不受损害。然而,肿瘤细胞和患者对TRAIL诱导的细胞凋亡的新兴抗性限制了其进一步的应用。在这项研究中,我们开发了一种嵌合蛋白膜联蛋白V-TRAIL(命名为TP8),在体外和体内均比TRAIL具有更高的功效。在体外,TP8在一系列肿瘤细胞上的EC50远低于野生型TRAIL。膜联蛋白V为该重组蛋白提供了更高的功效,同时由于TP8对正常细胞没有影响,所以TRAIL的肿瘤特异性保持不变。在体内,TP8有效抑制了涉及多种癌细胞类型(包括A549,Colo205和Bel7402)的小鼠异种移植物中的肿瘤生长,并延长了肿瘤加倍时间和肿瘤生长延迟时间。这项研究提供了治疗TRAIL耐药癌症的新的合理策略。

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