Regenerative Medicine Program, Ottawa Hospital Research Institute, Ottawa, ON K1H 8L6, Canada.
Department of Biochemistry, Microbiology, and Immunology, Faculty of Medicine, University of Ottawa, Ottawa, ON K1N 6N5, Canada.
Int J Mol Sci. 2024 Nov 20;25(22):12451. doi: 10.3390/ijms252212451.
Human adenovirus (HAdV)-based oncolytic vectors, which are designed to preferentially replicate in and kill cancer cells, have shown modest efficacy in human clinical trials in part due to poor viral distribution throughout the tumor mass. Previously, we showed that expression of the p14 fusion-associated small transmembrane (FAST) fusogenic protein could enhance oncolytic HAdV efficacy and reduce tumor growth rate in a human xenograft mouse model of cancer. We now explore whether co-expression of the adenovirus death protein (ADP) with p14 FAST protein could synergize to further enhance oncolytic vector efficacy. ADP is naturally encoded within the early region 3 (E3) of HAdV, a region which is frequently removed from HAdV-based vectors, and functions to enhance cell lysis and progeny release. We evaluated a variety of approaches to achieve optimal expression of the two proteins, the most efficient method being insertion of an expression cassette within the E3 deletion, consisting of the coding sequences for p14 FAST protein and ADP separated by a self-cleaving peptide derived from the porcine teschovirus-1 (P2A). However, the quantities of p14 FAST protein and ADP produced from this vector were reduced approximately 10-fold compared to a similar vector-expressing only p14 FAST protein and wildtype HAdV, respectively. Compared to our original oncolytic vector-expressing p14 FAST protein alone, reduced expression of p14 FAST protein and ADP from the P2A construct reduced cell-cell fusion, vector spread, and cell-killing activity in human A549 adenocarcinoma cells in culture. These studies show that a self-cleaving peptide can be used to express two different transgenes in an armed oncolytic HAdV vector, but also highlight the challenges in maintaining adequate transgene expression when modifying vector design.
人腺病毒(HAdV)-基于溶瘤病毒,旨在优先在和杀死癌细胞中复制,已显示出适度的疗效在人体临床试验部分由于病毒分布不良在整个肿瘤块中。以前,我们表明表达 p14 融合相关小跨膜(FAST)融合蛋白可以增强溶瘤 HAdV 的疗效并降低癌症异种移植小鼠模型中的肿瘤生长速度。我们现在探讨腺病毒死亡蛋白(ADP)与 p14 FAST 蛋白的共表达是否可以协同作用以进一步增强溶瘤载体的疗效。ADP 天然编码在 HAdV 的早期区域 3(E3)中,该区域经常从 HAdV 基载体中去除,并具有增强细胞裂解和后代释放的功能。我们评估了实现两种蛋白最佳表达的各种方法,最有效的方法是在 E3 缺失内插入一个表达盒,该表达盒由 p14 FAST 蛋白和 ADP 的编码序列组成,由来自猪口蹄疫病毒-1(P2A)的自切割肽隔开。然而,与仅表达 p14 FAST 蛋白和野生型 HAdV 的类似载体相比,该载体产生的 p14 FAST 蛋白和 ADP 的量减少了约 10 倍。与我们最初表达 p14 FAST 蛋白的溶瘤载体相比,来自 P2A 构建体的 p14 FAST 蛋白和 ADP 的表达减少降低了细胞-细胞融合、载体扩散和细胞杀伤活性在人 A549 腺癌细胞中的活性。这些研究表明,自切割肽可用于表达武装溶瘤 HAdV 载体中的两种不同转基因,但也突出了在修改载体设计时保持足够转基因表达的挑战。