Department of Pathology, Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Department of Oncology, Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
J Pathol. 2018 Dec;246(4):395-404. doi: 10.1002/path.5154.
Pancreatic cancer arises from noninvasive precursor lesions, including pancreatic intraepithelial neoplasia (PanIN), intraductal papillary mucinous neoplasm (IPMN), and mucinous cystic neoplasm (MCN), which are curable if detected early enough. Recently, these types of precursor lesions have been extensively characterized at the molecular level, defining the timing of critical genetic alterations in tumorigenesis pathways. The results of these studies deepen our understanding of tumorigenesis in the pancreas, providing novel insights into tumor initiation and progression. Perhaps more importantly, they also provide a rational foundation for early detection approaches that could allow clinical intervention prior to malignant transformation. In this review, we summarize the results of comprehensive molecular characterization of PanINs, IPMNs, and MCNs and discuss the implications for cancer biology as well as early detection. Copyright © 2018 Pathological Society of Great Britain and Ireland. Published by John Wiley & Sons, Ltd.
胰腺癌起源于非浸润性的前体病变,包括胰腺上皮内瘤变(PanIN)、导管内乳头状黏液性肿瘤(IPMN)和黏液性囊腺瘤(MCN),如果早期发现,这些病变是可治愈的。最近,这些前体病变在分子水平上得到了广泛的描述,确定了肿瘤发生途径中关键遗传改变的时间。这些研究的结果加深了我们对胰腺发生的理解,为肿瘤的发生和进展提供了新的见解。也许更重要的是,它们也为早期检测方法提供了合理的基础,从而可以在恶性转化之前进行临床干预。在这篇综述中,我们总结了 PanINs、IPMNs 和 MCNs 的全面分子特征描述的结果,并讨论了其对癌症生物学和早期检测的意义。版权所有 © 2018 英国和爱尔兰病理学会。由 John Wiley & Sons, Ltd. 出版。