Gray Mark E, Sullivan Paul, Marland Jamie R K, Greenhalgh Stephen N, Meehan James, Gregson Rachael, Clutton R Eddie, Cousens Chris, Griffiths David J, Murray Alan, Argyle David
The Royal (Dick) School of Veterinary Studies and Roslin Institute, University of Edinburgh, Easter Bush, Edinburgh, United Kingdom.
Cancer Research UK Edinburgh Centre and Division of Pathology Laboratories, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, United Kingdom.
Front Oncol. 2019 Jun 19;9:534. doi: 10.3389/fonc.2019.00534. eCollection 2019.
cell line and murine models have historically dominated pre-clinical cancer research. These models can be expensive and time consuming and lead to only a small percentage of anti-cancer drugs gaining a license for human use. Large animal models that reflect human disease have high translational value; these can be used to overcome current pre-clinical research limitations through the integration of drug development techniques with surgical procedures and anesthetic protocols, along with emerging fields such as implantable medical devices. Ovine pulmonary adenocarcinoma (OPA) is a naturally-occurring lung cancer that is caused by the jaagsiekte sheep retrovirus. The disease has similar histological classification and oncogenic pathway activation to that of human lung adenocarcinomas making it a valuable model for studying human lung cancer. Developing OPA models to include techniques used in the treatment of human lung cancer would enhance its translational potential, making it an excellent research tool in assessing cancer therapeutics. In this study we developed a novel OPA model to validate the ability of miniaturized implantable O and pH sensors to monitor the tumor microenvironment. Naturally-occurring pre-clinical OPA cases were obtained through an on-farm ultrasound screening programme. Sensors were implanted into OPA tumors of anesthetized sheep using a CT-guided trans-thoracic percutaneous implantation procedure. This study reports the findings from 9 sheep that received sensor implantations. Time taken from initial CT scans to the placement of a single sensor into an OPA tumor was 45 ± 5 min, with all implantations resulting in the successful delivery of sensors into tumors. Immediate post-implantation mild pneumothoraces occurred in 4 sheep, which was successfully managed in all cases. This is, to the best of our knowledge, the first description of the use of naturally-occurring OPA cases as a pre-clinical surgical model. Through the integration of techniques used in the treatment of human lung cancer patients, including ultrasound, general anesthesia, CT and surgery into the OPA model, we have demonstrated its translational potential. Although our research was tailored specifically for the implantation of sensors into lung tumors, we believe the model could also be developed for other pre-clinical applications.
细胞系和小鼠模型在历史上一直主导着临床前癌症研究。这些模型可能成本高昂且耗时,并且只有一小部分抗癌药物能够获得人类使用许可。反映人类疾病的大型动物模型具有很高的转化价值;通过将药物开发技术与外科手术及麻醉方案相结合,以及与可植入医疗设备等新兴领域相结合,这些模型可用于克服当前临床前研究的局限性。绵羊肺腺癌(OPA)是一种由绵羊肺腺瘤病毒引起的自然发生的肺癌。该疾病在组织学分类和致癌途径激活方面与人类肺腺癌相似,使其成为研究人类肺癌的有价值模型。开发包含用于治疗人类肺癌技术的OPA模型将增强其转化潜力,使其成为评估癌症治疗方法的优秀研究工具。在本研究中,我们开发了一种新型OPA模型,以验证小型化可植入氧和pH传感器监测肿瘤微环境的能力。通过农场超声筛查计划获得自然发生的临床前OPA病例。使用CT引导的经胸经皮植入程序将传感器植入麻醉绵羊的OPA肿瘤中。本研究报告了9只接受传感器植入的绵羊的研究结果。从最初的CT扫描到将单个传感器植入OPA肿瘤的时间为45±5分钟,所有植入均成功将传感器输送到肿瘤中。4只绵羊在植入后立即出现轻度气胸,所有病例均成功处理。据我们所知,这是首次描述将自然发生的OPA病例用作临床前手术模型。通过将用于治疗人类肺癌患者的技术,包括超声、全身麻醉、CT和手术整合到OPA模型中,我们展示了其转化潜力。尽管我们的研究专门针对将传感器植入肺肿瘤进行,但我们相信该模型也可用于其他临床前应用。