Maria Consiglia Bragazzi

ORCID: 0000-0003-3626-8546
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About
Contact & Profiles
Research Areas
  • Cholangiocarcinoma and Gallbladder Cancer Studies
  • Cancer Genomics and Diagnostics
  • Pediatric Hepatobiliary Diseases and Treatments
  • Liver Diseases and Immunity
  • Gallbladder and Bile Duct Disorders
  • Pancreatic and Hepatic Oncology Research
  • Liver Disease Diagnosis and Treatment
  • Liver physiology and pathology
  • Genetic factors in colorectal cancer
  • Drug Transport and Resistance Mechanisms
  • RNA modifications and cancer
  • Ferroptosis and cancer prognosis
  • Peptidase Inhibition and Analysis
  • Cancer-related molecular mechanisms research
  • Metabolism, Diabetes, and Cancer
  • Cancer-related Molecular Pathways
  • Cancer Cells and Metastasis
  • Eosinophilic Esophagitis
  • RNA Research and Splicing
  • Metastasis and carcinoma case studies
  • Cancer Diagnosis and Treatment
  • Epigenetics and DNA Methylation
  • Lung Cancer Treatments and Mutations
  • Cancer, Hypoxia, and Metabolism
  • Helicobacter pylori-related gastroenterology studies

Sapienza University of Rome
2014-2024

Ospedale Santa Maria Goretti
2020

Policlinico Umberto I
2018

Medico
2012

Ospedale Regina Margherita
2010-2011

University of L'Aquila
2007

Texas A&M University System
2007

Marche Polytechnic University
2007

University of Milan
2007

Ospedale San Paolo
2007

Farshad Farshidfar Siyuan Zheng Marie‐Claude Gingras Yulia Newton Juliann Shih and 95 more A. Gordon Robertson Toshinori Hinoue Katherine A. Hoadley Ewan A. Gibb Jason Roszik Kyle R. Covington Chia-Chin Wu Eve Shinbrot Nicolas Stransky Apurva M. Hegde Ju Dong Yang Ed Reznik Sara Sadeghi Chandra Sekhar Pedamallu Akinyemi I. Ojesina Julian M. Hess J. Todd Auman Suhn K. Rhie Reanne Bowlby Mitesh J. Borad Andrew X. Zhu Joshua M. Stuart Chris Sander Rehan Akbani Andrew D. Cherniack Vikram Deshpande Taofic Mounajjed Wai Chin Foo Michael Torbenson David E. Kleiner Peter W. Laird David A. Wheeler Autumn J. McRee Oliver F. Bathe Jesper B. Andersen Nabeel Bardeesy Lewis R. Roberts Lawrence N. Kwong Rehan Akbani Loretta K. Allotey Adrian Ally Domenico Alvaro Jesper B. Andersen Elizabeth L. Appelbaum Arshi Arora J. Todd Auman Miruna Balasundaram Saianand Balu Nabeel Bardeesy Oliver F. Bathe Stephen B. Baylin Rameen Beroukhim Mario Berríos Tom Bodenheimer Lori Boice Arnoud Boot Mitesh J. Borad Jay Bowen Reanne Bowlby Maria Consiglia Bragazzi Denise Brooks Vincenzo Cardinale Rebecca Carlsen Guido Carpino André Lopes Carvalho Roongruedee Chaiteerakij Vishal C. Chandan Andrew D. Cherniack Lynda Chin Juok Cho Gina Choe Eric Chuah Sudha Chudamani Carrie Cibulskis Matthew G. Cordes Kyle R. Covington Daniel Crain Erin Curley Agostino Maria De Rose Timothy Defreitas John A. Demchok Vikram Deshpande Noreen Dhalla Li Ding Kimberley Evason Farshad Farshidfar Ina Felau Martin L. Ferguson Wai Chin Foo Antonio Franchitto Scott Frazer Catrina C. Fronick Lucinda A. Fulton Robert S. Fulton Stacey Gabriel

Cholangiocarcinoma (CCA) is an aggressive malignancy of the bile ducts, with poor prognosis and limited treatment options. Here, we describe integrated analysis somatic mutations, RNA expression, copy number, DNA methylation by The Cancer Genome Atlas a set predominantly intrahepatic CCA cases propose molecular classification scheme. We identified IDH mutant-enriched subtype distinct features including low expression chromatin modifiers, elevated mitochondrial genes, increased number....

10.1016/j.celrep.2017.02.033 article EN cc-by Cell Reports 2017-03-01

Cholangiocarcinoma (CCA) is a malignant tumour, arising from biliary epithelium at any portion of the tree, characterized by bad prognosis and poor response to current therapies. CCA currently classified as intrahepatic (IH-CCA) or extrahepatic (EH-CCA). The distinction between IH-CCA EH-CCA has become increasingly important, epidemiological features (i.e., incidence risk factors), biologic pathologic characteristics clinical course are largely different. New insights into hepatic tree stem...

10.3978/j.issn.2224-4778.2011.11.04 article EN Translational gastrointestinal cancer 2012-03-01
Rosanna Asselta Elvezia Maria Paraboschi Alessio Gerussi Heather J. Cordell George Mells and 95 more Richard Sandford David Jones Minoru Nakamura Kazuko Ueno Yuki Hitomi Minae Kawashima Nao Nishida Katsushi Tokunaga Masao Nagasaki Atsushi Tanaka Ruqi Tang Zhiqiang Li Yongyong Shi Xiangdong Liu Ma Xiong Gideon M. Hirschfield Katherine A. Siminovitch Marco Carbone Giulia Cardamone Stefano Duga M. Eric Gershwin Michael F. Seldin Pietro Invernizzi Erin J. Walker Gang Xie Andy Mason Robert P. Myers Kevork Peltekian Cameron N. Ghent Elizabeth J. Atkinson Bruce Juran Kostas Lazaridis Yue Lu Xiangjun Gu Kaiyan Jing Chris Amos Andrea Affronti Maurizia Rossana Brunetto B. Coco Giancarlo Spinzi G. Elia Carlo Ferrari Ana Lleò Luigi Muratori Paolo Muratori Piero Portincasa Agostino Colli Savino Bruno Guido Colloredo Francesco Azzaroli Pietro Andreoné Maria Consiglia Bragazzi Domenico Alvaro Vincenzo Cardinale Nora Cazzagon Cristina Rigamonti Annarosa Floreani F. Rosina Antonio Ciaccio Laura Cristoferi Daphne D’Amato Federica Malinverno Clara Mancuso Sara Massironi Chiara Milani Sarah Elisabeth O’Donnell Vincenzo Ronca Donatella Barisani Pietro Lampertico Francesco Donato S. Fagiuoli Piero Luigi Almasio Edoardo G. Giannini C. Cursaro Massimo Colombo Luca Valenti Luca Miele Angelo Andriulli Grazia Anna Niro Ignazio Grattagliano Lorenzo Morini Giovanni Casella M. Vinci Pier Maria Battezzati Andrea Crosignani Massimo Zuin Alberto Mattalia V. Calvaruso Sílvia Colombo A. Benedetti Marco Marzioni Andrea Galli Fabio Marra Mirko Tarocchi A. Picciotto

10.1053/j.gastro.2021.02.061 article EN Gastroenterology 2021-03-04

Objective Primary sclerosing cholangitis (PSC) is a genetically complex, inflammatory bile duct disease of largely unknown aetiology often leading to liver transplantation or death. Little known about the genetic contribution severity and progression PSC. The aim this study identify variants associated with PSC development complications. Design We collected standardised subphenotypes in large cohort 3402 patients After quality control, we combined 130 422 single nucleotide polymorphisms all...

10.1136/gutjnl-2016-313598 article EN Gut 2017-08-04

Cholangiocarcinoma (CCA) is an aggressive cancer with high resistance to chemotherapeutics. CCA enriched in stem cells, which correlate aggressiveness and prognosis. FXR, a member of the metabolic nuclear receptor family, markedly down-regulated human CCA. Our aim was evaluate, primary cultures intrahepatic (iCCA), effects FXR agonist obeticholic acid (OCA), semisynthetic bile derivative, on their cancerogenic potential. Primary iCCA cell were prepared from surgical specimens mucinous or...

10.1371/journal.pone.0210077 article EN cc-by PLoS ONE 2019-01-24

In the treatment of upper GI endoscopy-negative patients with heartburn and epigastric pain or burning, antacids, antireflux agents, mucosal protective agents are widely used, alone as add-on treatment, to increase response proton-pump inhibitors, which not indicated in infancy pregnancy account for significant cost expenditure.

10.14309/ajg.0000000000002360 article EN cc-by-nc-nd The American Journal of Gastroenterology 2023-06-12

Background: Cholangiocarcinoma cells express and secrete insulin-like growth factor I (IGF-I) vascular endothelial (VEGF). Objective: To measure IGF-I VEGF in bile serum of patients with extrahepatic cholangiocarcinoma to evaluate their performance as diagnostic markers. Design: Cross-sectional study. Setting: Inpatients at the Division Gastroenterology, University Hospital, Ancona, Italy. Patients: 73 who consecutively had endoscopic retrograde cholangiopancreatography (ERCP), including (n...

10.7326/0003-4819-147-7-200710020-00003 article EN Annals of Internal Medicine 2007-10-02

We investigated the sensitivity of intrahepatic cholangiocarcinoma (IHCCA) subtypes to chemotherapeutics and molecular targeted agents. Primary cultures mucin- mixed-IHCCA were prepared from surgical specimens (N. 18 IHCCA patients) evaluated for cell proliferation (MTS assay) apoptosis (Caspase 3) after incubation (72 hours) with increasing concentrations different drugs. In vivo, subcutaneous human tumor xenografts evaluated. characterized by a pattern expression cancer stem markers, drug...

10.1371/journal.pone.0142124 article EN cc-by PLoS ONE 2015-11-16

Cholangiocarcinoma (CCA) is a very aggressive cancer showing the presence of high stem cells (CSCs). Doublecortin-like kinase1 (DCLK1) has been demonstrated as CSC marker in different gastroenterological solid tumors. Our aim was to evaluate vitro expression and biological function DCLK1 intrahepatic CCA (iCCA) perihilar (pCCA).Specimens surgically resected human were enzymatically digested, submitted immunosorting for specific markers (LGR5 [leucine-rich repeat-containing G protein-coupled...

10.1002/hep.31571 article EN cc-by-nc-nd Hepatology 2020-09-26

Cholangiocarcinoma (CCA) and its subtypes (mucin- mixed-CCA) arise from the neoplastic transformation of cholangiocytes, epithelial cells lining biliary tree. CCA has a high mortality rate owing to aggressiveness, late diagnosis resistance radiotherapy chemotherapeutics. We have demonstrated that is enriched for cancer stem which express mesenchymal transition (EMT) traits, with these features being associated aggressiveness drug resistance. TGF-β signaling upregulated in involved EMT....

10.1371/journal.pone.0183932 article EN cc-by PLoS ONE 2017-09-05
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