Nasca Vincenzo, Chiaravalli Marta, Piro Geny, Esposito Annachiara, Salvatore Lisa, Tortora Giampaolo, Corbo Vincenzo, Carbone Carmine
Department of Medical Oncology, Fondazione Policlinico Universitario Agostino Gemelli IRCCS, 00168 Rome, Italy.
Medical Oncology, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
Int J Mol Sci. 2020 Sep 2;21(17):6386. doi: 10.3390/ijms21176386.
Pancreatic ductal adenocarcinoma is one of the most lethal human cancers. Its precursor lesions include pancreatic intra-epithelial neoplasia, mucinous cystic neoplasm, and intraductal papillary mucinous neoplasm (IPMN). IPMNs usually present as an incidental finding at imaging in 2.6% of the population and, according to the degree of dysplasia, they are classified as low- or high-grade lesions. Since the risk of malignant transformation is not accurately predictable, the management of these lesions is based on morphological and clinical parameters, such as presence of mural nodule, main pancreatic duct dilation, presence of symptoms, or high-grade dysplasia. Although the main genetic alterations associated to IPMNs have been elucidated, they are still not helpful for disease risk stratification. The growing body of genomic and epigenomic studies along with the more recent development of organotypic cultures provide the opportunity to improve our understanding of the malignant transformation process, which will likely deliver biomarkers to help discriminate between low- and high-risk lesions. Recent insights on the topic are herein summarized.
胰腺导管腺癌是最致命的人类癌症之一。其前驱病变包括胰腺上皮内瘤变、黏液性囊性肿瘤和导管内乳头状黏液性肿瘤(IPMN)。IPMN通常在影像学检查中偶然发现,占人群的2.6%,根据发育异常程度,它们被分类为低级别或高级别病变。由于恶性转化的风险无法准确预测,这些病变的管理基于形态学和临床参数,如壁结节的存在、主胰管扩张、症状的存在或高级别发育异常。尽管与IPMN相关的主要基因改变已得到阐明,但它们仍无助于疾病风险分层。基因组学和表观基因组学研究的不断增加,以及最近器官型培养的发展,为增进我们对恶性转化过程的理解提供了机会,这可能会产生生物标志物,以帮助区分低风险和高风险病变。本文总结了关于该主题的最新见解。