Coutermarsh-Ott Sheryl L, Broadway Katherine M, Scharf Birgit E, Allen Irving C
Virginia Tech, VA-MD College of Veterinary Medicine, Department of Biomedical Sciences and Pathobiology, Blacksburg, VA, USA.
Virginia Tech, Department of Biological Sciences, Blacksburg, VA, USA.
Oncotarget. 2017 May 16;8(20):33601-33613. doi: 10.18632/oncotarget.16830.
A variety of bacterial strains have been evaluated as bio-therapeutic and immunomodulatory agents to treat cancer. One such strain, Salmonella enterica serovar Typhimurium VNP20009, which is attenuated by a purine auxotrophic mutation and modified lipid A, is characterized in previous models as a safely administered, tumor colonizing agent. However, earlier work tended to use less aggressive cancer cell lines and immunocompromised animal models. Here, we investigated the safety and efficacy of VNP20009 in a highly malignant murine model of human breast cancer. Additionally, as VNP20009 has recently been found to have a defective chemotaxis system, we tested whether restoring chemotaxis would improve anti-cancer properties in this model system. Exposure to VNP20009 had no significant effect on primary mammary tumor size or pulmonary metastasis, and the tumor colonizing process appeared chemotaxis independent. Moreover, tumor-bearing mice exposed to Salmonella exhibited increased morbidity that was associated with significant liver disease. Our results suggest that VNP20009 may not be safe or efficacious when used in aggressive, metastatic breast cancer models utilizing immunocompetent animals.
多种细菌菌株已被评估作为生物治疗和免疫调节药物用于治疗癌症。其中一种菌株,鼠伤寒沙门氏菌血清型鼠伤寒VNP20009,通过嘌呤营养缺陷型突变和修饰的脂多糖A减毒,在先前的模型中被表征为一种安全给药的肿瘤定植剂。然而,早期的研究倾向于使用侵袭性较小的癌细胞系和免疫缺陷动物模型。在此,我们研究了VNP20009在高度恶性的人乳腺癌小鼠模型中的安全性和有效性。此外,由于最近发现VNP20009具有缺陷的趋化系统,我们测试了恢复趋化性是否会改善该模型系统中的抗癌特性。暴露于VNP20009对原发性乳腺肿瘤大小或肺转移没有显著影响,并且肿瘤定植过程似乎与趋化性无关。此外,暴露于沙门氏菌的荷瘤小鼠发病率增加,这与严重的肝脏疾病有关。我们的结果表明,当在使用免疫健全动物的侵袭性转移性乳腺癌模型中使用时,VNP20009可能不安全或无效。