Mucinous cystic neoplasms and simple mucinous cysts are two distinct precursors of pancreatic cancer: clinicopathological, genomic, and transcriptomic characterization.

IF 5.6 2区 医学 Q1 ONCOLOGY
Antonio Pea, Michele Bevere, Anastasios Gkountakos, Davide Pasini, Denise Fiorini, Andrea Mafficini, Stela Golovco, Michele Simbolo, Serena Pedron, Concetta Sciammarella, Paola Mattiolo, Aldo Mombello, Manuela Villanova, Carlotta Franzina, Francesca Masetto, Calogero Ciulla, Nicola Sperandio, Kohei Fujikura, Masha S Ahadi, Jaswinder S Samra, Amber L Johns, Joanne Verheij, Martijn W J Stommel, Hjalmar van Santvoort, Leonor Schubert Santana, Giuseppe Malleo, Michele Milella, Lodewijk A A Brosens, Laura D Wood, David K Chang, Riccardo De Robertis, Mirko D'Onofrio, Anthony J Gill, Roberto Salvia, Vincenzo Corbo, Rita T Lawlor, Aldo Scarpa, Claudio Luchini
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引用次数: 0

Abstract

Mucinous cystic neoplasms (MCNs) of the pancreas are macroscopic precursors of pancreatic cancer. A similar cystic lesion but lacking the ovarian-type subepithelial stroma has been recently defined as a simple mucinous cyst (SMC); however, its nature remains unclear. This study aims to define the clinicopathological and molecular profiles of a cohort of MCNs and SMCs of the pancreas and their associated invasive carcinoma. Overall, 23 cases were identified, comprising 19 MCNs and 4 SMCs with co-occurring invasive carcinoma. A multiregional (two samples from each cystic lesion and one from the adenocarcinoma) DNA and RNA sequencing approach was used. The key findings can be summarized as follows: (1) Molecular association: In 22/23 cases (95.7%), the concomitant mucinous cyst and invasive carcinoma shared specific genomic alterations, establishing for the first time that SMC is a true precursor of pancreatic cancer. (2) Clinical behavior: carcinomas arising from SMC appeared to be more aggressive than those arising from MCN. (3) Mutational profile: both cyst types showed significant similarities to conventional pancreatic ductal adenocarcinoma (PDAC), with KRAS and TP53 the most commonly altered genes. (4) Intracystic heterogeneity: while most molecular alterations were present in both analyzed cystic areas, RNF43 showed the highest heterogeneity. (5) CDKN2A: its alterations were predominantly restricted to the invasive component, suggesting a role in driving the invasion in a subset of cases. CNKN2A may also serve as a potential biomarker for identifying high-risk cysts. (6) RNAseq: most cases showed a switch from the classical to the basal transcriptome subtype during the progression from cystic neoplasms to invasive cancers. These findings establish SMCs as new precursors of pancreatic cancer and provide critical insights into the tumorigenesis of MCNs, with potential immediate implications for tumor taxonomy and clinical management. © 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

粘液囊性肿瘤和单纯性粘液囊肿是胰腺癌的两种不同的前体:临床病理学、基因组学和转录组学特征。
胰腺粘液囊性肿瘤(mcn)是胰腺癌的宏观前兆。类似的囊性病变,但缺乏卵巢型上皮下基质,最近被定义为单纯性粘液囊肿(SMC);然而,其性质仍不清楚。本研究旨在确定胰腺mcn和SMCs及其相关浸润性癌的临床病理和分子特征。总共发现23例,包括19例mcn和4例SMCs合并浸润性癌。采用多区域(每个囊性病变两个样本,腺癌一个样本)DNA和RNA测序方法。主要发现如下:(1)分子关联:22/23例(95.7%)伴有粘液囊肿和浸润性癌具有特异性的基因组改变,首次证实SMC是胰腺癌的真正前兆。(2)临床行为:SMC引起的癌似乎比MCN引起的癌更具侵袭性。(3)突变谱:两种囊肿类型与常规胰腺导管腺癌(pancreatic ductal adenocarcinoma, PDAC)有显著的相似性,其中KRAS和TP53是最常见的改变基因。(4)囊内异质性:虽然在分析的两个囊区中都存在大多数分子改变,但RNF43的异质性最高。(5) CDKN2A:它的改变主要局限于侵袭性成分,这表明在一部分病例中,它在驱动侵袭中起作用。CNKN2A也可能作为识别高风险囊肿的潜在生物标志物。(6) RNAseq:大多数病例在囊性肿瘤向浸润性癌症的进展过程中表现出从经典转录组亚型向基础转录组亚型的转换。这些发现确立了SMCs作为胰腺癌的新前体,并为MCNs的肿瘤发生提供了重要的见解,对肿瘤分类和临床管理具有潜在的直接意义。©2025作者。《病理学杂志》由John Wiley & Sons Ltd代表大不列颠和爱尔兰病理学会出版。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
The Journal of Pathology
The Journal of Pathology 医学-病理学
CiteScore
14.10
自引率
1.40%
发文量
144
审稿时长
3-8 weeks
期刊介绍: The Journal of Pathology aims to serve as a translational bridge between basic biomedical science and clinical medicine with particular emphasis on, but not restricted to, tissue based studies. The main interests of the Journal lie in publishing studies that further our understanding the pathophysiological and pathogenetic mechanisms of human disease. The Journal of Pathology welcomes investigative studies on human tissues, in vitro and in vivo experimental studies, and investigations based on animal models with a clear relevance to human disease, including transgenic systems. As well as original research papers, the Journal seeks to provide rapid publication in a variety of other formats, including editorials, review articles, commentaries and perspectives and other features, both contributed and solicited.
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