Igase Masaya, Hwang Chung Chew, Kambayashi Satoshi, Kubo Masato, Coffey Matt, Miyama Takako Shimokawa, Baba Kenji, Okuda Masaru, Noguchi Shunsuke, Mizuno Takuya
Laboratory of Molecular Diagnostics and Therapeutics (Igase, Noguchi, Mizuno), Laboratory of Veterinary Internal Medicine (Kambayashi, Miyama, Baba, Okuda), and Laboratory of Veterinary Pathology (Kubo), Joint Faculty of Veterinary Medicine and Laboratory of Molecular Diagnostics and Therapeutics (Hwang) and Biomedical Science Center for Translational Research (Okuda, Noguchi, Mizuno), United Graduate School of Veterinary Science, Yamaguchi University, 1677-1 Yoshida, Yamaguchi 753-8515, Japan; Oncolytics Biotech Inc., Calgary, Alberta (Coffey).
Can J Vet Res. 2016 Jan;80(1):21-31.
The oncolytic effects of reovirus in various cancers have been proven in many clinical trials in human medicine. Oncolytic virotherapy using reovirus for canine cancers is being developed in our laboratory. The objective of this study was to examine the synergistic anti-cancer effects of a combination of reovirus and low doses of various chemotherapeutic agents on mammary gland tumors (MGTs) in dogs. The first part of this study demonstrated the efficacy of reovirus in canine MGTs in vitro and in vivo. Reovirus alone exerted significant cell death by means of caspase-dependent apoptosis in canine MGT cell lines. A single injection of reovirus impeded growth of canine MGT tumors in xenografted mice, but was insufficient to induce complete tumor regression. The second part of this study highlighted the anti-tumor effects of reovirus in combination with low doses of paclitaxel, carboplatin, gemcitabine, or toceranib. Enhanced synergistic activity was observed in the MGT cell line treated concomitantly with reovirus and in all the chemotherapeutic agents except toceranib. In addition, combining reovirus with paclitaxel or gemcitabine at half dosage of half maximal inhibitory concentration (IC50) enhanced cytotoxicity by activating caspase 3. Our data suggest that the combination of reovirus and low dose chemotherapeutic agents provides an attractive option in canine cancer therapy.
呼肠孤病毒在多种癌症中的溶瘤作用已在人类医学的许多临床试验中得到证实。我们实验室正在研发使用呼肠孤病毒治疗犬类癌症的溶瘤病毒疗法。本研究的目的是检验呼肠孤病毒与低剂量多种化疗药物联合使用对犬乳腺肿瘤(MGT)的协同抗癌作用。本研究的第一部分证明了呼肠孤病毒在体外和体内对犬MGT的疗效。单独使用呼肠孤病毒通过半胱天冬酶依赖性凋亡在犬MGT细胞系中引起显著的细胞死亡。单次注射呼肠孤病毒可抑制异种移植小鼠中犬MGT肿瘤的生长,但不足以诱导肿瘤完全消退。本研究的第二部分强调了呼肠孤病毒与低剂量紫杉醇、卡铂、吉西他滨或托西拉尼联合使用的抗肿瘤作用。在与呼肠孤病毒同时处理的MGT细胞系以及除托西拉尼之外的所有化疗药物中均观察到增强的协同活性。此外,将呼肠孤病毒与半最大抑制浓度(IC50)一半剂量的紫杉醇或吉西他滨联合使用可通过激活半胱天冬酶3增强细胞毒性。我们的数据表明,呼肠孤病毒与低剂量化疗药物联合使用为犬类癌症治疗提供了一个有吸引力的选择。