Akbay Esra A, Kim James
Department of Pathology, University of Texas Southwestern, Dallas, TX 75208, USA.
Harold C. Simmons Comprehensive Cancer Center, University of Texas Southwestern, Dallas, TX 75208, USA.
Transl Lung Cancer Res. 2018 Aug;7(4):464-486. doi: 10.21037/tlcr.2018.06.04.
Lung cancer accounts for the greatest number of cancer deaths in the world. Tobacco smoke-associated cancers constitute the majority of lung cancer cases but never-smoker cancers comprise a significant and increasing fraction of cases. Recent genomic and transcriptomic sequencing efforts of lung cancers have revealed distinct sets of genetic aberrations of smoker and never-smoker lung cancers that implicate disparate biology and therapeutic strategies. Autochthonous mouse models have contributed greatly to our understanding of lung cancer biology and identified novel therapeutic targets and strategies in the era of targeted therapy. With the emergence of immuno-oncology, mouse models may continue to serve as valuable platforms for novel biological insights and therapeutic strategies. Here, we will review the variety of available autochthonous mouse models of lung cancer, their relation to human smoker and never-smoker lung cancers, and their application to immuno-oncology and immune checkpoint blockade that is revolutionizing lung cancer therapy.
肺癌是全球癌症死亡人数最多的癌症。与烟草烟雾相关的癌症占肺癌病例的大多数,但从不吸烟的肺癌患者所患癌症在病例中占相当大且不断增加的比例。最近对肺癌进行的基因组和转录组测序研究揭示了吸烟和从不吸烟的肺癌患者不同的基因畸变组合,这意味着不同的生物学特性和治疗策略。自发小鼠模型极大地促进了我们对肺癌生物学的理解,并在靶向治疗时代确定了新的治疗靶点和策略。随着免疫肿瘤学的出现,小鼠模型可能会继续作为获取新生物学见解和治疗策略的宝贵平台。在这里,我们将综述现有的各种肺癌自发小鼠模型、它们与人类吸烟和从不吸烟的肺癌的关系,以及它们在免疫肿瘤学和正在彻底改变肺癌治疗的免疫检查点阻断中的应用。