Testa Joseph R, Berns Anton
Cancer Biology Program, Fox Chase Cancer Center, Philadelphia, PA, United States.
Division of Molecular Genetics, The Netherlands Cancer Institute, Amsterdam, Netherlands.
Front Oncol. 2020 Feb 11;10:101. doi: 10.3389/fonc.2020.00101. eCollection 2020.
Rodent models of malignant mesothelioma help facilitate the understanding of the biology of this highly lethal cancer and to develop and test new interventions. Introducing the same genetic lesions as found in human mesothelioma in mice results in tumors that show close resemblance with the human disease counterpart. This includes the extensive inflammatory responses that characterize human malignant mesothelioma. The relatively fast development of mesothelioma in mice when the appropriate combination of lesions is introduced, with or without exposure to asbestos, make the autochthonous models particularly useful for testing new treatment strategies in an immunocompetent setting, whereas Patient-Derived Xenograft models are particularly useful to assess effects of inter- and intra-tumor heterogeneity and human-specific features of mesothelioma. It is to be expected that new insights obtained by studying these experimental systems will lead to new more effective treatments for this devastating disease.
恶性间皮瘤的啮齿动物模型有助于促进对这种高致死性癌症生物学特性的理解,并开发和测试新的干预措施。在小鼠中引入与人类间皮瘤相同的基因损伤会导致肿瘤,这些肿瘤与人类疾病相似。这包括人类恶性间皮瘤所特有的广泛炎症反应。当引入适当的损伤组合时,无论是否接触石棉,小鼠中间皮瘤的相对快速发展使得原位模型对于在免疫活性环境中测试新的治疗策略特别有用,而患者来源的异种移植模型对于评估肿瘤间和肿瘤内异质性以及间皮瘤的人类特异性特征的影响特别有用。预计通过研究这些实验系统获得的新见解将为这种毁灭性疾病带来新的更有效的治疗方法。