Robert H Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, 303 East Superior Street, Chicago, IL 60611, USA.
Cancer Prev Res (Phila). 2010 Nov;3(11):1382-7. doi: 10.1158/1940-6207.CAPR-10-0258. Epub 2010 Nov 2.
With the advent of mouse models that recapitulate the cellular and molecular pathology of pancreatic neoplasia and cancer, it is now feasible to recruit and deploy these models for the evaluation of various chemopreventive and/or anticancer regimens. The highly lethal nature of pancreatic ductal adenocarcinoma (PDAC) makes multiple areas of research a priority, including assessment of compounds that prevent or suppress the development of early lesions that can transform into PDAC. Currently, there are over a dozen models available, which range from homogeneous preneoplastic lesions with remarkable similarity to human pancreatic intraepithelial neoplasms to models with a more heterogeneous population of lesions including cystic papillary and mucinous lesions. The molecular features of these models may also vary in a manner comparable with the differences observed in lesion morphology, and so, navigating the route of model selection is not trivial. Yet, arming the community of cancer investigators with a repertoire of models and the guidance to select relevant models that fit their research themes promises to produce findings that will have clinical relevance.
随着能够重现胰腺肿瘤和癌症细胞及分子病理学的小鼠模型的出现,现在可以招募和利用这些模型来评估各种化学预防和/或抗癌方案。胰腺导管腺癌 (PDAC) 的高致命性使其成为多个研究领域的重点,包括评估预防或抑制可能转化为 PDAC 的早期病变发展的化合物。目前,有十几种模型可供选择,这些模型范围从与人类胰腺上皮内瘤变具有显著相似性的同质癌前病变到具有更异质病变群体的模型,包括囊性乳头和黏液性病变。这些模型的分子特征也可能以类似于病变形态观察到的差异的方式发生变化,因此,选择模型的途径并不简单。然而,为癌症研究人员提供一系列模型并指导他们选择符合其研究主题的相关模型,有望产生具有临床相关性的发现。