TY - JOUR
T1 - Identification of spatially-resolved markers of malignant transformation in Intraductal Papillary Mucinous Neoplasms
AU - Agostini, Antonio
AU - Piro, Geny
AU - Inzani, Frediano
AU - Quero, Giuseppe
AU - Esposito, Annachiara
AU - Caggiano, Alessia
AU - Priori, Lorenzo
AU - Larghi, Alberto Leonardo
AU - Alfieri, Sergio
AU - Casolino, Raffaella
AU - Scaglione, Giulia
AU - Tondolo, Vincenzo
AU - Cammarota, Giovanni
AU - Ianiro, Gianluca
AU - Corbo, Vincenzo
AU - Biankin, Andrew V.
AU - Tortora, Giampaolo
AU - Carbone, Carmine
PY - 2024
Y1 - 2024
N2 - The existing Intraductal Papillary Mucinous Neoplasm (IPMN) risk stratification relies on clinical and histological factors, resulting in inaccuracies and leading to suboptimal treatment. This is due to the lack of appropriate molecular markers that can guide patients toward the best therapeutic options. Here, we assess and confirm subtype-specific markers for IPMN across two independent cohorts of patients using two Spatial Transcriptomics (ST) technologies. Specifically, we identify HOXB3 and ZNF117 as markers for Low-Grade Dysplasia, SPDEF and gastric neck cell markers in borderline cases, and NKX6-2 and gastric isthmus cell markers in High-Grade-Dysplasia Gastric IPMN, highlighting the role of TNF alpha and MYC activation in IPMN progression and the role of NKX6-2 in the specific Gastric IPMN progression. In conclusion, our work provides a step forward in understanding the gene expression landscapes of IPMN and the critical transcriptional networks related to PDAC progression.The current stratification of Intraductal Papillary Mucinous Neoplasms (IPMN) is based on clinical and histological features rather than molecular ones. Here, the authors use spatial transcriptomics to characterise IPMN patient samples, and identify markers associated with progression to pancreatic cancer.
AB - The existing Intraductal Papillary Mucinous Neoplasm (IPMN) risk stratification relies on clinical and histological factors, resulting in inaccuracies and leading to suboptimal treatment. This is due to the lack of appropriate molecular markers that can guide patients toward the best therapeutic options. Here, we assess and confirm subtype-specific markers for IPMN across two independent cohorts of patients using two Spatial Transcriptomics (ST) technologies. Specifically, we identify HOXB3 and ZNF117 as markers for Low-Grade Dysplasia, SPDEF and gastric neck cell markers in borderline cases, and NKX6-2 and gastric isthmus cell markers in High-Grade-Dysplasia Gastric IPMN, highlighting the role of TNF alpha and MYC activation in IPMN progression and the role of NKX6-2 in the specific Gastric IPMN progression. In conclusion, our work provides a step forward in understanding the gene expression landscapes of IPMN and the critical transcriptional networks related to PDAC progression.The current stratification of Intraductal Papillary Mucinous Neoplasms (IPMN) is based on clinical and histological features rather than molecular ones. Here, the authors use spatial transcriptomics to characterise IPMN patient samples, and identify markers associated with progression to pancreatic cancer.
KW - pancreas
KW - pancreas
UR - http://hdl.handle.net/10807/280120
U2 - 10.1038/s41467-024-46994-2
DO - 10.1038/s41467-024-46994-2
M3 - Article
SN - 2041-1723
VL - 15
SP - 1
EP - 16
JO - Nature Communications
JF - Nature Communications
ER -
