Acuna Sergio A, Ottolino-Perry Kathryn, Çako Besmira, Tang Nan, Angarita Fernando A, McCart J Andrea
Division of Experimental Therapeutics, Toronto General Research Institute, University Health Network, Toronto, ON, Canada.
Ann Surg Oncol. 2014 Jul;21(7):2259-66. doi: 10.1245/s10434-014-3651-4. Epub 2014 Apr 10.
Malignant peritoneal mesothelioma (MPM) is an aggressive cancer with a dismal prognosis. Oncolytic viruses are a promising new therapy for cancer because of their ability to kill tumor cells with minimal toxicity to normal tissues. This experimental study aimed to examine the potential of modified vaccinia virus (VV) to treat MPM when administered alone or as an adjuvant treatment to surgery.
Two aggressive murine mesothelioma cell lines (AC29, AB12), were used. Cell viability and viral cytopathic effects were assessed using MTS and crystal violet assays. Immunocompetent mice were injected intraperitoneally with MPM cells and treated with intraperitoneal VV. Tumor-bearing mice also underwent cytoreductive surgery (CRS) followed by VV (or control) therapy.
The cytotoxic effects of VV on MPM cell lines was significantly increased compared with the control non-cancer cell line. In both orthotopic models, VV induced tumor regression, prolonging median and long-term survival. VV treatment after incomplete CRS was not superior to VV alone; however, when mice with microscopic disease were treated with VV, further prolongation of median and long-term survivals was observed.
VV selectively kills MPM cells in vitro and leads to improved survival and cures in immunocompetent murine models. Higher efficacy of the virus in the microscopic disease context suggests the use of the virus as an adjuvant treatment to complete surgical resection. These promising results justify further studies of VV in humans as a novel treatment for MPM.
恶性腹膜间皮瘤(MPM)是一种侵袭性癌症,预后不佳。溶瘤病毒是一种很有前景的新型癌症治疗方法,因为它们能够杀死肿瘤细胞,同时对正常组织的毒性最小。本实验研究旨在探讨改良痘苗病毒(VV)单独给药或作为手术辅助治疗时治疗MPM的潜力。
使用两种侵袭性小鼠间皮瘤细胞系(AC29、AB12)。使用MTS和结晶紫测定法评估细胞活力和病毒细胞病变效应。将免疫活性小鼠腹腔注射MPM细胞,并用腹腔内VV治疗。荷瘤小鼠还接受了减瘤手术(CRS),随后进行VV(或对照)治疗。
与对照非癌细胞系相比,VV对MPM细胞系的细胞毒性作用显著增加。在两种原位模型中,VV均诱导肿瘤消退,延长中位生存期和长期生存期。不完全CRS后进行VV治疗并不优于单独使用VV;然而,当对微小疾病小鼠用VV治疗时,观察到中位生存期和长期生存期进一步延长。
VV在体外选择性杀死MPM细胞,并在免疫活性小鼠模型中提高生存率并实现治愈。病毒在微小疾病情况下的更高疗效表明可将病毒用作完全手术切除的辅助治疗。这些有前景的结果证明有必要进一步研究将VV作为MPM的一种新的治疗方法应用于人类。