Popper Helmut H
Institute of Pathology, Research Unit Molecular Lung & Pleura Pathology, Medical University of Graz, Auenbruggerplatz 25, 8036, Graz, Austria,
Methods Mol Biol. 2015;1267:19-43. doi: 10.1007/978-1-4939-2297-0_2.
A few human tumor types have been modeled in mice using genetic or chemical tools. The final goal of these efforts is to establish models that mimic not only the location and cellular origin of human cancers but also their genetic aberrations and morphologic appearances. The latter has been neglected by most investigators, and comparative histopathology of human versus mouse cancers is not readily available. This issue is exacerbated by the fact that some human malignancies comprise a whole spectrum of cancer subtypes that differ molecularly and morphologically. Lung cancer is a paradigm that appears not only as non-small cell and small-cell lung cancer but comprises a plethora of subtypes with distinct morphologic features. This review discusses species-specific and common morphological features of non-small cell lung cancer in mice and humans. Potential inconsistencies and the need for refined genetic tools are discussed in the context of a comparative analysis between commonly employed RAS-induced mouse tumors and human lung cancers.
已经使用遗传或化学工具在小鼠中建立了几种人类肿瘤模型。这些研究的最终目标是建立不仅能模拟人类癌症的位置和细胞起源,还能模拟其基因畸变和形态外观的模型。大多数研究人员忽略了后者,而且人类与小鼠癌症的比较组织病理学资料并不容易获得。由于一些人类恶性肿瘤包含一系列在分子和形态上不同的癌症亚型,这个问题变得更加严重。肺癌就是一个范例,它不仅表现为非小细胞肺癌和小细胞肺癌,还包含大量具有不同形态特征的亚型。本综述讨论了小鼠和人类非小细胞肺癌的物种特异性和共同形态特征。在对常用的RAS诱导的小鼠肿瘤和人类肺癌进行比较分析的背景下,讨论了潜在的不一致性以及对精细遗传工具的需求。