Laboratory of Infectious Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA.
Curr Top Microbiol Immunol. 2021;430:161-181. doi: 10.1007/82_2017_79.
Human lung cancer is one of the leading causes of death worldwide, with nearly 2 million of new cases diagnosed each year, often too late for a successful therapeutic intervention. In this chapter, organotypic models of lung cancer will be reviewed. Ex vivo tissue explants, spheroids, organoids, and novel bioengineering approaches are currently being used to study human lung cancer. Although there is no ideal method that will fully recapitulate the complex human lung architecture, the three-dimensional (3D) organotypic models described here represent a major advance from classical two-dimensional (2D) tissue culture models. Organotypic tissue cultures are better at predicting in vivo tissue responses to anticancer drugs or carcinogenic toxins. In addition, there is also a possibility to use these systems as part of personalized medicine (e.g., to assist clinicians in selecting appropriate therapeutic choices based on individual patient-derived tissue responses to drugs in vitro). There is still a need for improvement in the 3D culture systems, such as automation for high-throughput testing and reduction of costs. However, given the large number of failed clinical trials due to safety or efficacy reasons, more attention should be given to these more physiologically relevant 3D organotypic tissue culture models.
人肺癌是全球主要致死病因之一,每年新诊断病例近 200 万例,通常为时已晚,无法进行成功的治疗干预。本章将综述肺癌的器官型模型。目前,离体组织外植体、球体、类器官和新型生物工程方法正被用于研究人肺癌。尽管没有一种理想的方法能完全重现复杂的人肺癌结构,但这里描述的三维(3D)器官型模型代表了对经典二维(2D)组织培养模型的重大改进。器官型组织培养在预测抗癌药物或致癌毒素对体内组织的反应方面表现更佳。此外,还有可能将这些系统用作个体化医疗的一部分(例如,协助临床医生根据个体患者对药物的体外组织反应来选择合适的治疗选择)。3D 培养系统仍需要改进,例如高通量测试的自动化和成本降低。然而,鉴于大量临床试验因安全性或疗效原因而失败,应更加关注这些更具生理相关性的 3D 器官型组织培养模型。