Vincenzo Corbo

ORCID: 0000-0002-6340-8009
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About
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Research Areas
  • Pancreatic and Hepatic Oncology Research
  • Cancer Genomics and Diagnostics
  • Cancer Cells and Metastasis
  • Neuroendocrine Tumor Research Advances
  • Epigenetics and DNA Methylation
  • Cancer Immunotherapy and Biomarkers
  • Lung Cancer Research Studies
  • Lung Cancer Treatments and Mutations
  • Phagocytosis and Immune Regulation
  • Renal and related cancers
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Immune cells in cancer
  • Genetic factors in colorectal cancer
  • PI3K/AKT/mTOR signaling in cancer
  • RNA modifications and cancer
  • Neuroblastoma Research and Treatments
  • Pancreatic function and diabetes
  • Genomics and Phylogenetic Studies
  • Immunotherapy and Immune Responses
  • Genomics and Chromatin Dynamics
  • Extracellular vesicles in disease
  • Cancer Research and Treatments
  • Cancer-related molecular mechanisms research
  • Genomics and Rare Diseases
  • Protein Degradation and Inhibitors

University of Verona
2016-2025

Agostino Gemelli University Polyclinic
2021

University of L'Aquila
2021

Istituto Dermopatico dell'Immacolata
2021

Catholic University of America
2021

Istituti di Ricovero e Cura a Carattere Scientifico
2021

Istituto Tumori Bari
2021

University Hospital Foundation
2019-2021

CS Diagnostics
2021

Lustgarten Foundation
2014-2019

Peter J. Bailey David K. Chang Kátia Nones Amber L. Johns Ann‐Marie Patch and 95 more Marie‐Claude Gingras David K. Miller Angelika N. Christ Timothy J. C. Bruxner Michael C. Quinn Craig Nourse L. Charles Murtaugh Ivon Harliwong Senel Idrisoglu Suzanne Manning Ehsan Nourbakhsh Shivangi Wani J. Lynn Fink Oliver Holmes Venessa Chin Matthew J. Anderson Stephen H. Kazakoff Conrad Leonard Felicity Newell Nick M. Waddell Scott Wood Qinying Xu Peter J. Wilson Nicole Cloonan Karin S. Kassahn Darrin F. Taylor Kelly Quek Alan J. Robertson Lorena Pantano Laura Mincarelli Luis Navarro-Sánchez Lisa Evers Jianmin Wu Mark Pinese Mark J. Cowley Marc D. Jones Emily K. Colvin Adnan M. Nagrial Emily S. Humphrey Lorraine A. Chantrill Amanda Mawson Jeremy L. Humphris Angela Chou Marina Pajic Christopher J. Scarlett Andreia V. Pinho Marc Giry-Laterrière Ilse Rooman Jaswinder S. Samra James G. Kench Jessica A. Lovell Neil D. Merrett Christopher W. Toon Krishna Epari Nam Q. Nguyen Andrew P. Barbour Nikolajs Zeps Kim Moran‐Jones Nigel B. Jamieson Janet Graham Fraser R. Duthie Karin A. Oien Jane Hair Robert Grützmann Anirban Maitra Christine A. Iacobuzio‐Donahue Christopher L. Wolfgang Richard A. Morgan Rita T. Lawlor Vincenzo Corbo Claudio Bassi Borislav C. Rusev Paola Capelli Roberto Salvia Giampaolo Tortora Debabrata Mukhopadhyay Gloria M. Petersen Donna M. Munzy William E. Fisher Saadia A. Karim James R. Eshleman Ralph H. Hruban Christian Pilarsky Jennifer P. Morton Owen J. Sansom Aldo Scarpa Elizabeth A. Musgrove Ulla‐Maja Bailey Oliver Hofmann Robert L. Sutherland David A. Wheeler Anthony J. Gill Richard A. Gibbs John V. Pearson Nicola Waddell

10.1038/nature16965 article EN Nature 2016-02-23

10.1038/nature14169 article EN Nature 2015-02-24

Pancreatic stellate cells (PSCs) differentiate into cancer-associated fibroblasts (CAFs) that produce desmoplastic stroma, thereby modulating disease progression and therapeutic response in pancreatic ductal adenocarcinoma (PDA). However, it is unknown whether CAFs uniformly carry out these tasks or if subtypes of with distinct phenotypes PDA exist. We identified a CAF subpopulation elevated expression α-smooth muscle actin (αSMA) located immediately adjacent to neoplastic mouse human...

10.1084/jem.20162024 article EN cc-by The Journal of Experimental Medicine 2017-02-23
Aldo Scarpa David K. Chang Kátia Nones Vincenzo Corbo Ann‐Marie Patch and 95 more Peter J. Bailey Rita T. Lawlor Amber L. Johns David K. Miller Andrea Mafficini Borislav C. Rusev Maria Scardoni Davide Antonello Stefano Barbi Katarzyna Sikora Sara Cingarlini Caterina Vicentini Skye McKay Michael C. Quinn Timothy J. C. Bruxner Angelika N. Christ Ivon Harliwong Senel Idrisoglu Suzanne McLean Craig Nourse Ehsan Nourbakhsh Peter J. Wilson Matthew J. Anderson J. Lynn Fink Felicity Newell Nick M. Waddell Oliver Holmes Stephen H. Kazakoff Conrad Leonard Scott Wood Qinying Xu Shivashankar H. Nagaraj Eliana Amato Irene Dalai Samantha Bersani Ivana Cataldo Angelo Paolo Dei Tos Paola Capelli Maria Vittoria Davì Luca Landoni Anna Malpaga Marco Miotto Vicki Whitehall Barbara Leggett Janelle L. Harris Jonathan M. Harris Marc D. Jones Jeremy L. Humphris Lorraine A. Chantrill Venessa Chin Adnan Nagrial Marina Pajic Christopher J. Scarlett Andreia V. Pinho Ilse Rooman Christopher W. Toon Jianmin Wu Mark Pinese Mark J. Cowley Andrew P. Barbour Amanda Mawson Emily S. Humphrey Emily K. Colvin Angela Chou Jessica A. Lovell Nigel B. Jamieson Fraser R. Duthie Marie‐Claude Gingras William E. Fisher Rebecca A. Dagg Loretta M. S. Lau Michael Lee Hilda A. Pickett Roger R. Reddel Jaswinder S. Samra James G. Kench Neil D. Merrett Krishna Epari Nam Q. Nguyen Nikolajs Zeps Massimo Falconi Michele Simbolo Giovanni Butturini George Van Buren Stefano Partelli Matteo Fassan Kum Kum Khanna Anthony J. Gill David A. Wheeler Richard A. Gibbs Elizabeth A. Musgrove Claudio Bassi Giampaolo Tortora Paolo Pederzoli John V. Pearson

10.1038/nature21063 article EN Nature 2017-02-14

Histopathological samples are a treasure-trove of DNA for clinical research. However, the quality can vary depending on source or extraction method applied. Thus standardized and cost-effective workflow qualification preparations is essential to guarantee interlaboratory reproducible results. The process consists quantification double strand (dsDNA) assessment its suitability downstream applications, such as high-throughput next-generation sequencing. We tested two most frequently used...

10.1371/journal.pone.0062692 article EN cc-by PLoS ONE 2013-06-06
Claire Vennin Pauline Mélénec Romain Rouet Max Nobis Aurélie Cazet and 95 more Kendelle J. Murphy David Herrmann Daniel A. Reed Morghan C. Lucas Sean Warren Zehra Elgundi Mark Pinese Gabriella Kalna Daniel Roden Monisha Samuel Anaiis Zaratzian Shane T. Grey Andrew Da Silva Wilfred Leung Amber L. Johns Lorraine A. Chantrill Angela Chou Angela Steinmann Mehreen Arshi Tanya Dwarte Danielle Froio Brooke A. Pereira Shona Ritchie Cecilia R Chambers Xanthe Metcalf Nicola Waddell John V. Pearson Ann-Marie Patch Katia Nones Felicity Newell Pamela Mukhopadhyay Venkateswar Addala Stephen H. Kazakoff Oliver Holmes Conrad Leonard Scott Wood Sean M. Grimmond Oliver Hofmann Angelika N. Christ Timothy J. C. Bruxner Jaswinder S. Samra Nick Pavlakis Hilda High Ray Asghari Neil D. Merrett Darren Pavey Amitabha Das Peter H. Cosman Kasim Ismail Chelsie O’Connnor Alina Stoita David M. Williams Allan Spigellman Vincent Lam Duncan McLeod Judy Kirk James G. Kench Peter Grimison Caroline Cooper Charbel Sandroussi Annabel Goodwin R. Scott Mead Katherine Tucker Lesley Andrews Michael Texler Cindy Forest Krishna Epari Mo Ballal David Fletcher Sanjay Mukhedkar Nikolajs Zeps Maria Beilin Kynan Feeney Nan Q. Nguyen Andrew Ruszkiewicz Chris Worthley John Chen Mark E. Brooke‐Smith Virginia Papangelis Andrew D. Clouston Andrew P. Barbour Thomas O’Rourke Jonathan W. Fawcett Kellee Slater Michael Hatzifotis Peter Hodgkinson Mehrdad Nikfarjam James R. Eshleman Ralph H. Hruban Christopher L. Wolfgang Rita T. Lawlor Stefania Beghelli Vincenzo Corbo Maria Scardoni Claudio Bassi

Abstract Heterogeneous subtypes of cancer-associated fibroblasts (CAFs) coexist within pancreatic cancer tissues and can both promote restrain disease progression. Here, we interrogate how cells harboring distinct alterations in p53 manipulate CAFs. We reveal the existence a p53-driven hierarchy, where with gain-of-function (GOF) mutant educate dominant population CAFs that establish pro-metastatic environment for GOF null alike. also demonstrate educated by may be reprogrammed either or...

10.1038/s41467-019-10968-6 article EN cc-by Nature Communications 2019-08-12

The importance of epigenetic modifications such as DNA methylation in tumorigenesis is increasingly being appreciated. To define the genome-wide pattern pancreatic ductal adenocarcinomas (PDAC), we captured profiles 167 untreated resected PDACs and compared them to a panel 29 adjacent nontransformed pancreata using high-density arrays. A total 11,634 CpG sites associated with 3,522 genes were significantly differentially methylated (DM) PDAC capable segregating from non-malignant pancreas,...

10.1002/ijc.28765 article EN cc-by-nc International Journal of Cancer 2014-02-05

Next-generation sequencing (NGS) was applied to 148 lung neuroendocrine tumours (LNETs) comprising the four World Health Organization classification categories: 53 typical carcinoid (TCs), 35 atypical (ACs), 27 large-cell carcinomas, and 33 small-cell carcinomas. A discovery screen conducted on 46 samples by use of whole-exome high-coverage targeted 418 genes. Eighty-eight recurrently mutated genes from both current literature were verified in cases screen, validated additional 102 LNETs...

10.1002/path.4853 article EN cc-by The Journal of Pathology 2016-11-22

10.1053/j.gastro.2016.09.060 article EN Gastroenterology 2016-11-15

// Michele Simbolo 1,2,* , Matteo Fassan Andrea Ruzzenente 3,* Mafficini 1 Laura D. Wood 4 Vincenzo Corbo Davide Melisi 5 Giuseppe Malleo 6 Caterina Vicentini Giorgio Malpeli 1,3,6 Antonello Nicola Sperandio Paola Capelli 2 Anna Tomezzoli Calogero Iacono 3 Rita T. Lawlor 1,2 Claudio Bassi Ralph H. Hruban Alfredo Guglielmi Giampaolo Tortora Filippo de Braud 7 Aldo Scarpa ARC-Net Research Centre, University and Hospital Trust of Verona, Italy Department Pathology Diagnostics, Surgery, General...

10.18632/oncotarget.1943 article EN Oncotarget 2014-05-01

<h3>Background</h3> Pancreatic ductal adenocarcinoma (PDAC) is a highly devastating disease with an overall 5-year survival rate of less than 8%. New evidence indicates that PDAC cells release pro-inflammatory metabolites induce marked alteration normal hematopoiesis, favoring the expansion and accumulation myeloid-derived suppressor (MDSCs). We report here patients show increased levels both circulating tumor-infiltrating MDSC-like cells. <h3>Methods</h3> The frequency MDSC subsets in...

10.1186/s40425-019-0734-6 article EN cc-by Journal for ImmunoTherapy of Cancer 2019-09-18

Objective Recent studies have found aristaless-related homeobox gene (ARX)/pancreatic and duodenal 1 (PDX1), alpha-thalassemia/mental retardation X-linked (ATRX)/death domain-associated protein (DAXX) alternative lengthening of telomeres (ALT) to be promising prognostic biomarkers for non-functional pancreatic neuroendocrine tumours (NF-PanNETs). However, they not been comprehensively evaluated, especially among small NF-PanNETs (≤2.0 cm). Moreover, their status in (NETs) from other sites...

10.1136/gutjnl-2020-322595 article EN cc-by-nc Gut 2021-04-13

Purpose Individuals with adenocarcinoma of the ampulla Vater demonstrate a broad range outcomes, presumably because these cancers may arise from any one three epithelia that converge at location. This variability poses challenges for clinical decision making and development novel therapeutic strategies. Patients Methods We assessed potential utility histomolecular phenotypes defined using combination histopathology protein expression (CDX2 MUC1) in 208 patients independent cohorts who...

10.1200/jco.2012.46.8868 article EN Journal of Clinical Oncology 2013-02-26

Pancreatic endocrine tumors (PETs) may be part of hereditary multiple neoplasia type 1 (MEN1) syndrome. While MEN1 gene mutation is the only ascertained genetic anomaly described in PETs, no data exist on cellular localization MEN1-encoded protein, menin, normal pancreas and PETs. A total 169 PETs were used to assess i) mutational status 100 clinically sporadic by direct DNA sequencing, ii) immunohistochemical expression menin 140 including 71 cases screened for mutations, iii) correlation...

10.1677/erc-10-0028 article EN Endocrine Related Cancer 2010-06-22

Abstract The CRISPR/Cas9 system is a powerful tool for studying gene function. Here, we describe method that allows temporal control of activity based on conditional Cas9 destabilization. We demonstrate fusing an FKBP12-derived destabilizing domain to (DD-Cas9) enables expression and editing in the presence FKBP12 synthetic ligand. This can be easily adapted co-express, from same promoter, DD-Cas9 with any other interest without co-modulation latter. In particular, when co-expressed...

10.1038/ncomms14370 article EN cc-by Nature Communications 2017-02-22

DNA mutational profiling showed that atypical carcinoids (ACs) share alterations with large cell neuroendocrine carcinomas (LCNECs). Transcriptomic studies suggested LCNECs are composed of two subtypes, one which shares molecular anomalies SCLC. The missing piece information is the transcriptomic relationship between ACs and LCNECs, as a direct comparison lacking in literature.Transcriptomic genomic were investigated by next-generation sequencing discovery set 14 validated on 21 18 using...

10.1016/j.jtho.2019.05.003 article EN cc-by-nc-nd Journal of Thoracic Oncology 2019-05-11

Abstract The existing Intraductal Papillary Mucinous Neoplasm (IPMN) risk stratification relies on clinical and histological factors, resulting in inaccuracies leading to suboptimal treatment. This is due the lack of appropriate molecular markers that can guide patients toward best therapeutic options. Here, we assess confirm subtype-specific for IPMN across two independent cohorts using Spatial Transcriptomics (ST) technologies. Specifically, identify HOXB3 ZNF117 as Low-Grade Dysplasia,...

10.1038/s41467-024-46994-2 article EN cc-by Nature Communications 2024-03-29

Abstract Purpose: KRAS is mutated in the majority of pancreatic ductal adenocarcinoma. MAPK and PI3K-AKT are primary effector pathways, but combined PI3K inhibition has not been demonstrated to be clinically effective date. We explore resistance mechanisms uniquely employed by malignant cells. Experimental Design: evaluated expression activation receptor tyrosine kinases response MEK AKT KPC mice organoids. In addition, we sought determine therapeutic efficacy targeting pathways induced...

10.1158/1078-0432.ccr-19-1398 article EN Clinical Cancer Research 2019-09-06

Background Complex tumor and immune microenvironment render pancreatic ductal adenocarcinoma (PDAC) resistant to checkpoint inhibitors (ICIs). Therefore, a strategy convert the hostile into an immunopermissive is required. Recent studies showed that intratumoral injection of Toll-like receptor 9 agonist IMO-2125 primes adaptive response. Phase I II trials with demonstrated its safety antitumoral activity. Methods We generated array preclinical models by orthotopically engrafting PDAC-derived...

10.1136/jitc-2021-002876 article EN cc-by-nc Journal for ImmunoTherapy of Cancer 2021-09-01
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