Laboratory of Molecular and Genetic Therapeutics, Institute of Advanced Medical Science, Hyogo Medical University, Hyogo 663-8501, Japan.
Departments of Biomedical Chemistry, School of Science and Technology, Kwansei Gakuin University, Hyogo 669-1330, Japan.
Int J Mol Sci. 2023 Oct 2;24(19):14823. doi: 10.3390/ijms241914823.
Retroviral replicating vectors (RRVs) selectively replicate and can specifically introduce prodrug-activating genes into tumor cells, whereby subsequent prodrug administration induces the death of the infected tumor cells. We assessed the ability of two distinct RRVs generated from amphotropic murine leukemia virus (AMLV) and gibbon ape leukemia virus (GALV), which infect cells via type-III sodium-dependent phosphate transporters, PiT-2 and PiT-1, respectively, to infect human gastric cancer (GC) cells. A quantitative RT-PCR showed that all tested GC cell lines had higher expression levels of PiT-2 than PiT-1. Accordingly, AMLV, encoding a green fluorescent protein gene, infected and replicated more efficiently than GALV in most GC cell lines, whereas both RRVs had a low infection rate in human fibroblasts. RRV encoding a cytosine deaminase prodrug activator gene, which converts the prodrug 5-flucytosine (5-FC) to the active drug 5-fluorouracil, showed that AMLV promoted superior 5-FC-induced cytotoxicity compared with GALV, which correlated with the viral receptor expression level and viral spread. In MKN-74 subcutaneous xenograft models, AMLV had significant antitumor effects compared with GALV. Furthermore, in the MKN-74 recurrent tumor model in which 5-FC was discontinued, the resumption of 5-FC administration reduced the tumor volume. Thus, RRV-mediated prodrug activator gene therapy might be beneficial for treating human GC.
逆转录病毒复制载体(RRV)具有选择性复制能力,并能将前药激活基因特异性地引入肿瘤细胞,随后给予前药会诱导感染的肿瘤细胞死亡。我们评估了两种源自嗜性鼠白血病病毒(AMLV)和长臂猿白血病病毒(GALV)的不同 RRV 的能力,这两种病毒分别通过 III 型钠离子依赖磷酸盐转运体 PiT-2 和 PiT-1 感染细胞,以感染人胃癌(GC)细胞。定量 RT-PCR 显示,所有测试的 GC 细胞系的 PiT-2 表达水平均高于 PiT-1。因此,编码绿色荧光蛋白基因的 AMLV 在大多数 GC 细胞系中的感染和复制效率均高于 GALV,而两种 RRV 在人成纤维细胞中的感染率均较低。RRV 编码胞嘧啶脱氨酶前药激活基因,可将前药 5-氟胞嘧啶(5-FC)转化为活性药物 5-氟尿嘧啶,结果表明,与 GALV 相比,AMLV 促进了更优的 5-FC 诱导的细胞毒性,这与病毒受体表达水平和病毒传播相关。在 MKN-74 皮下异种移植模型中,与 GALV 相比,AMLV 具有显著的抗肿瘤作用。此外,在停止使用 5-FC 的 MKN-74 复发性肿瘤模型中,重新给予 5-FC 可减少肿瘤体积。因此,RRV 介导的前药激活基因治疗可能有益于治疗人类 GC。