Laboratory of Biochemistry and Molecular Biology, Graduate School of Pharmaceutical Sciences, Osaka University, Osaka, 565-0871, Japan.
Laboratory of Hepatocyte Regulation, National Institutes of Biomedical Innovation, Health and Nutrition, Osaka, 567-0085, Japan.
Cell Death Dis. 2020 Jul 23;11(7):570. doi: 10.1038/s41419-020-02782-6.
Virotherapy using oncolytic adenovirus is an effective anticancer strategy. However, the tumor selectivity of oncolytic adenoviruses is not enough high. To develop oncolytic adenovirus with a low risk of off-tumor toxicity, we constructed a photoactivatable oncolytic adenovirus (paOAd). In response to blue light irradiation, the expression of adenoviral E1 genes, which are necessary for adenoviral replication, is induced and replication of this adenovirus occurs. In vitro, efficient lysis of various human cancer cell lines was observed by paOAd infection followed by blue light irradiation. Importantly, there was no off-tumor toxicity unless the cells were irradiated by blue light. In vivo, tumor growth in a subcutaneous tumor model and a mouse model of liver cancer was significantly inhibited by paOAd infection followed by blue light irradiation. In addition, paOAd also showed a therapeutic effect on cancer stem cells. These results suggest that paOAd is useful as a safe and therapeutically effective cancer therapy.
溶瘤腺病毒治疗是一种有效的抗癌策略。然而,溶瘤腺病毒的肿瘤选择性还不够高。为了开发一种肿瘤毒性低的溶瘤腺病毒,我们构建了一种光激活溶瘤腺病毒(paOAd)。在蓝光照射下,腺病毒复制所必需的 E1 基因的表达被诱导,从而导致这种腺病毒的复制。体外实验中,paOAd 感染后再进行蓝光照射,可有效裂解各种人癌细胞系。重要的是,除非细胞受到蓝光照射,否则不会产生肿瘤外毒性。在体内,paOAd 感染后再进行蓝光照射可显著抑制皮下肿瘤模型和肝癌小鼠模型中的肿瘤生长。此外,paOAd 对肿瘤干细胞也有治疗作用。这些结果表明,paOAd 作为一种安全有效的癌症治疗方法具有应用价值。