Evidence map›Paper›PMID 40371932›Full record

ArticleThe Journal of pathology2025

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

Antonio Pea, Michele Bevere, Anastasios Gkountakos, Davide Pasini, Denise Fiorini, Andrea Mafficini, Stela Golovco, Michele Simbolo, Serena Pedron, Concetta Sciammarella and 28 more

Abstract read
In one paragraph

Article in The Journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. Mucinous cystic neoplasms of the pancreas demonstrateFrontiers in cell and developmental biology · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

38 authors.

Antonio PeaDepartment of General and Pancreatic Surgery-The Pancreas Institute, Verona University Hospital Trust, Verona, Italy.
Michele BevereARC-Net Research Center, University of Verona, Verona, Italy.ORCID 0000-0001-8778-0860
Anastasios GkountakosARC-Net Research Center, University of Verona, Verona, Italy.
Davide PasiniDepartment of Engineering for Innovation Medicine, University of Verona, Verona, Italy.
Denise FioriniDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Andrea MafficiniARC-Net Research Center, University of Verona, Verona, Italy.
Stela GolovcoARC-Net Research Center, University of Verona, Verona, Italy.
Michele SimboloDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Serena PedronDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Concetta SciammarellaDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Paola MattioloDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Aldo MombelloDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Manuela VillanovaDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Carlotta FranzinaDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Francesca MasettoARC-Net Research Center, University of Verona, Verona, Italy.
Calogero CiullaDepartment of Diagnostics and Public Health, Section of Pathology, University of Verona, Verona, Italy.
Nicola SperandioARC-Net Research Center, University of Verona, Verona, Italy.
Kohei FujikuraDepartment of Pathology, Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins School of Medicine, Baltimore, MD, USA.ORCID 0000-0002-0520-733X
Masha S AhadiRoyal North Shore Hospital, St Leonards, NSW, Australia.
Jaswinder S SamraRoyal North Shore Hospital, St Leonards, NSW, Australia.
Amber L JohnsThe Garvan Institute of Medical Research and The Kinghorn Cancer Centre, Darlinghurst, NSW, Australia.
Joanne VerheijDepartment of Pathology, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
Martijn W J StommelDepartment of Surgery, Radboud University Medical Center, Nijmegen, The Netherlands.
Hjalmar van SantvoortDepartment of Surgery, Regional Academic Cancer Center Utrecht, UMC Utrecht and St Antonius Hospital, Utrecht, Netherlands.
Leonor Schubert SantanaWolfson Wohl Cancer Research Centre, Research Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
Giuseppe MalleoDepartment of General and Pancreatic Surgery-The Pancreas Institute, Verona University Hospital Trust, Verona, Italy.
Michele MilellaDepartment of Engineering for Innovation Medicine, University of Verona, Verona, Italy.
Lodewijk A A BrosensDepartment of Pathology, UMC Utrecht, Utrecht University, Utrecht, and Department of Pathology, Radboud University Medical Center, Nijmegen, The Netherlands.ORCID 0000-0003-1341-8994
Laura D WoodDepartment of Pathology, Sol Goldman Pancreatic Cancer Research Center, Johns Hopkins School of Medicine, Baltimore, MD, USA.
David K ChangWolfson Wohl Cancer Research Centre, Research Institute of Cancer Sciences, University of Glasgow, Glasgow, UK.
Riccardo De RobertisDepartment of Diagnostics and Public Health, Section of Radiology, University of Verona, Verona, Italy.
Mirko D'OnofrioDepartment of Diagnostics and Public Health, Section of Radiology, University of Verona, Verona, Italy.
Anthony J GillRoyal North Shore Hospital, St Leonards, NSW, Australia.
Roberto SalviaDepartment of General and Pancreatic Surgery-The Pancreas Institute, Verona University Hospital Trust, Verona, Italy.
Vincenzo CorboDepartment of Engineering for Innovation Medicine, University of Verona, Verona, Italy.
Rita T LawlorARC-Net Research Center, University of Verona, Verona, Italy.
Aldo ScarpaARC-Net Research Center, University of Verona, Verona, Italy.ORCID 0000-0003-1678-739X
Claudio LuchiniARC-Net Research Center, University of Verona, Verona, Italy.ORCID 0000-0003-4901-4908

Funding

Associazione Italiana per la Ricerca sul Cancro 26343Associazione Italiana per la Ricerca sul Cancro 28054Associazione Italiana per la Ricerca sul Cancro 28801Associazione Italiana per la Ricerca sul Cancro 29829Fondazione Cassa di Risparmio di Verona Vicenza Belluno e Ancona 203885/2017Fondazione Italiana per la ricerca sulle Malattie del Pancreas J38D19000690001Italian Ministry of University and Research B53D23008010006
6 · The paper itself

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.

Indexed as

Biomarkers, TumorCarcinoma, Pancreatic DuctalNeoplasms, Cystic, Mucinous, and SerousPancreatic CystPancreatic NeoplasmsPrecancerous ConditionsTranscriptomeAdultAgedAged, 80 and overFemaleGene Expression ProfilingHumansMaleMiddle AgedMutationBiomarkers, TumorCDKN2AMCNMucinous cystic neoplasmpancreatic precursorsPDACRNF43simple mucinous cysttranscriptome

Identifiers

PMID40371932
PMCPMC12256392

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.