Mario Capasso

ORCID: 0000-0003-3306-1259
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About
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Research Areas
  • Neuroblastoma Research and Treatments
  • Cancer, Hypoxia, and Metabolism
  • Radiomics and Machine Learning in Medical Imaging
  • Glioma Diagnosis and Treatment
  • SARS-CoV-2 and COVID-19 Research
  • Ancient Mediterranean Archaeology and History
  • Classical Antiquity Studies
  • COVID-19 Clinical Research Studies
  • Lung Cancer Research Studies
  • Protein Degradation and Inhibitors
  • Liver Disease Diagnosis and Treatment
  • Ancient Egypt and Archaeology
  • Digital Holography and Microscopy
  • Archaeology and Historical Studies
  • Microfluidic and Bio-sensing Technologies
  • Health Systems, Economic Evaluations, Quality of Life
  • Cancer Treatment and Pharmacology
  • Historical, Religious, and Philosophical Studies
  • PARP inhibition in cancer therapy
  • Cell Image Analysis Techniques
  • Ubiquitin and proteasome pathways
  • Erythrocyte Function and Pathophysiology
  • Renaissance Literature and Culture
  • Signaling Pathways in Disease
  • Historical and Religious Studies of Rome

University of Naples Federico II
2016-2025

Ceinge Biotecnologie Avanzate (Italy)
2016-2025

Azienda Ospedaliera Ospedale Maggiore
2024-2025

Federico II University Hospital
2012-2024

Collaborative Group (United States)
2024

SDN Istituto di Ricerca Diagnostica e Nucleare
2009-2023

Istituti di Ricovero e Cura a Carattere Scientifico
2009-2023

University of Padua
2013-2023

University of Siena
2023

Azienda Socio Sanitaria Territoriale Grande Ospedale Metropolitano Niguarda
2023

Chiara Fallerini Sergio Daga Stefania Mantovani Elisa Benetti Nicola Picchiotti and 95 more Daniela Francisci Francesco Paciosi Elisabetta Schiaroli Margherita Baldassarri Francesca Fava Maria Palmieri Serena Ludovisi Francesco Castelli Eugenia Quirós-Roldán Massimo Vaghi Stefano Rusconi Matteo Siano Maria Bandini Ottavia Spiga Katia Capitani Simone Furini Francesca Mari Floriana Valentino Gabriella Doddato Annarita Giliberti Rossella Tita Sara Amitrano Mirella Bruttini Susanna Croci Ilaria Meloni Maria Antonietta Mencarelli Caterina Lo Rizzo Anna Maria Pinto Laura Di Sarno Giada Beligni Andréa Tommasi Nicola Iuso Francesca Montagnani Massimiliano Fabbiani Barbara Rossetti Giacomo Zanelli Elena Bargagli Laura Bergantini Miriana d’Alessandro Paolo Cameli David Bennett Federico Anedda Simona Marcantonio Sabino Scolletta Federico Franchi Maria Antonietta Mazzei Susanna Guerrini Edoardo Conticini Luca Cantarini Bruno Frediani Danilo Tacconi Chiara Spertilli Marco Feri Alice Donati Raffaele Scala Luca Guidelli Genni Spargi Marta Corridi Cesira Nencioni Leonardo Croci Gian Piero Caldarelli Maurizio Spagnesi Davide Romani Paolo Piacentini Elena Desanctis Silvia Cappelli Anna Canaccini Agnese Verzuri Valentina Anemoli Agostino Ognibene Antonella d’Arminio Monforte Federica Gaia Miraglia Massimo Girardis Sophie Venturelli Stefano Busani Andrea Cossarizza Andrea Antinori Alessandra Vergori Arianna Emiliozzi Arianna Gabrieli Agostino Riva Pier Giorgio Scotton Francesca Andretta Sandro Panese Renzo Scaggiante Francesca Gatti Saverio Giuseppe Parisi Stefano Baratti Melania Degli Antoni Matteo Della Monica Carmelo Piscopo Mario Capasso Roberta Russo Immacolata Andolfo Achille Iolascon

Background: Recently, loss-of-function variants in TLR7 were identified two families which COVID-19 segregates like an X-linked recessive disorder environmentally conditioned by SARS-CoV-2. We investigated whether the represent tip of iceberg a subset male patients. Methods: This is nested case-control study we compared participants with extreme phenotype selected from Italian GEN-COVID cohort SARS-CoV-2-infected (<60 y, 79 severe cases versus 77 control cases). applied LASSO Logistic...

10.7554/elife.67569 article EN cc-by eLife 2021-03-02

Abstract In recent months, Coronavirus disease 2019 (COVID-19) caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has spread throughout the world. COVID-19 patients show mild, moderate or symptoms with latter ones requiring access to specialized intensive care. SARS-CoV-2 infections, pathogenesis and progression have not been clearly elucidated yet, thus forcing development of many complementary approaches identify candidate cellular pathways involved in progression. Host...

10.1038/s41598-021-82426-7 article EN cc-by Scientific Reports 2021-02-03

Abstract Quantitative phase imaging has gained popularity in bioimaging because it can avoid the need for cell staining, which, some cases, is difficult or impossible. However, as a result, quantitative does not provide labelling of various specific intracellular structures. Here we show novel computational segmentation method based on statistical inference that makes possible techniques to identify nucleus. We demonstrate approach with refractive index tomograms stain-free cells...

10.1038/s41566-022-01096-7 article EN cc-by Nature Photonics 2022-11-10

Abstract The response to antiviral therapy is lower in hepatitis C virus (HCV) patients with genotype 1 than those 2. Overexpression of the suppressor cytokine signaling 3 (SOCS3) gene liver tissue associated a poorer treatment outcome chronic viral 1. Also, insulin resistance has been implicated nonresponse an anti-HCV treatment. To understand why HCV respond differently, we investigated SOCS3 expression, metabolic syndrome (MS), and cohort HCV-related hepatitis. A total 198 (108 90 2)...

10.1002/hep.21782 article EN Hepatology 2007-08-01

Neuroblastoma is a malignant neoplasm of the developing sympathetic nervous system that notable for its phenotypic diversity. High-risk patients typically have widely disseminated disease at diagnosis and poor survival probability, but low-risk frequently localized tumors are almost always cured with little or no chemotherapy. Our genome-wide association study (GWAS) has identified common variants within FLJ22536, BARD1, LMO1 as significantly associated neuroblastoma more robustly high-risk...

10.1371/journal.pgen.1002026 article EN cc-by PLoS Genetics 2011-03-17

TP53 is the most frequently mutated gene in human malignancies; however, de novo somatic mutations childhood embryonal cancers such as neuroblastoma are rare. We report on analysis of three independent case-control cohorts comprising 10290 individuals and demonstrate that rs78378222 rs35850753, rare germline variants linkage disequilibrium map to 3' untranslated region (UTR) 5' UTR Δ133 isoform TP53, respectively, robustly associated with (rs35850753: odds ratio [OR] = 2.7, 95% confidence...

10.1093/jnci/dju047 article EN JNCI Journal of the National Cancer Institute 2014-03-14

Several neuroblastoma (NB) susceptibility loci have been identified within LINC00340, BARD1, LMO1, DUSP12, HSD17B12, DDX4, IL31RA, HACE1 and LIN28B by genome-wide association (GWA) studies including European American individuals. To validate comprehensively evaluate the impact of NB variants on disease risk phenotype, we analyzed 16 single nucleotide polymorphisms (SNPs) in an Italian population (370 cases 809 controls). We assessed their regulatory activity gene expression lymphoblastoid...

10.1093/carcin/bgs380 article EN Carcinogenesis 2012-12-07

HIF1A (Hypoxia-Inducible-Factor 1A) expression in solid tumors is relevant to establish resistance therapeutic approaches. The use of compounds direct against hypoxia signaling and does not show clinical efficiency because changeable oxygen concentrations tumor areas. identification targets expressed both normoxia HIF1A/hypoxia signatures might meliorate the prognostic stratification successes patients with high-risk tumors. In this study, we conducted a combined analysis RNA DNA methylation...

10.1186/s12881-019-0767-1 article EN cc-by BMC Medical Genetics 2019-02-26

Abstract Circulating tumor cells (CTCs) are rare released from primary, metastatic, or recurrent tumors in the peripheral blood of cancer patients. CTCs isolation and their molecular characterization represent a new marker screening, diagnostic tool called “liquid biopsy” (LB). Compared to traditional tissue biopsy that is invasive does not reveal heterogeneity, LB noninvasive reflects “real‐time” dynamism drug sensitivity. In frame LB, paradigm based on single‐cell label‐free analysis...

10.1002/viw.20200034 article EN cc-by View 2020-08-27

The established risk factors of coronavirus disease 2019 (COVID-19) are advanced age, male sex, and comorbidities, but they do not fully explain the wide spectrum manifestations. Genetic implicated in host antiviral response provide for novel insights into its pathogenesis.We performed an in-depth genetic analysis chromosome 21 exploiting genome-wide association study data, including 6,406 individuals hospitalized COVID-19 902,088 controls with European ancestry from Host Genetics...

10.1016/j.isci.2021.102322 article EN cc-by-nc-nd iScience 2021-03-19

COVID-19 is a global threat that has spread since the end of 2019, causing severe clinical sequelae and deaths, in context world pandemic. The infection highly pathogenetic infectious SARS-CoV-2 coronavirus been proven to exert systemic effects impacting metabolism. Yet, metabolic pathways involved pathophysiology progression are still unclear. Here, we present results mass spectrometry-based targeted metabolomic analysis on cohort 52 hospitalized patients, classified according disease...

10.3390/ijms22179548 article EN International Journal of Molecular Sciences 2021-09-02
Stefania Mantovani Sergio Daga Chiara Fallerini Margherita Baldassarri Elisa Benetti and 95 more Nicola Picchiotti Francesca Fava Anna Gallí Silvia Zibellini Mirella Bruttini Maria Palmieri Susanna Croci Sara Amitrano Diana Alaverdian Katia Capitani Simone Furini Francesca Mari Ilaria Meloni Francesca Montagnani Mario Tumbarello Ilaria Rancan Massimiliano Fabbiani Barbara Rossetti Laura Bergantini Miriana d’Alessandro Paolo Cameli David Bennett Federico Anedda Simona Marcantonio Sabino Scolletta Federico Franchi Maria Antonietta Mazzei Susanna Guerrini Edoardo Conticini Luca Cantarini Bruno Frediani Danilo Tacconi Chiara Spertilli Raffaelli Marco Feri Alice Donati Raffaele Scala Luca Guidelli Genni Spargi Marta Corridi Cesira Nencioni Leonardo Croci Gian Piero Caldarelli Davide Romani Paolo Piacentini Maria Bandini Elena Desanctis Silvia Cappelli Anna Canaccini Agnese Verzuri Valentina Anemoli Manola Pisani Agostino Ognibene Alessandro Pancrazzi Maria Lorubbio Massimo Vaghi Antonella d’Arminio Monforte Federica Gaia Miraglia Raffaele Bruno Marco Vecchia Massimo Girardis Sophie Venturelli Stefano Busani Andrea Cossarizza Andrea Antinori Alessandra Vergori Arianna Emiliozzi Stefano Rusconi Matteo Siano Arianna Gabrieli Agostino Riva Daniela Francisci Elisabetta Schiaroli Francesco Paciosi Andrea Tommasi Pier Giorgio Scotton Francesca Andretta Sandro Panese Stefano Baratti Renzo Scaggiante Francesca Gatti Saverio Giuseppe Parisi Francesco Castelli Eugenia Quirós-Roldán Melania Degli Antoni Isabella Zanella Matteo Della Monica Carmelo Piscopo Mario Capasso Roberta Russo Immacolata Andolfo Achille Iolascon Giuseppe Fiorentino Massimo Carella Marco Castori Filippo Aucella

Abstract Toll-like receptors (TLR) are crucial components in the initiation of innate immune responses to a variety pathogens, triggering production pro-inflammatory cytokines and type I II interferons, which responsible for antiviral responses. Among different TLRs, TLR7 recognizes several single-stranded RNA viruses including SARS-CoV-2. We others identified rare loss-of-function variants X-chromosomal young men with severe COVID-19 no prior history major chronic diseases, that were...

10.1038/s41435-021-00157-1 article EN cc-by Genes and Immunity 2021-12-24

Abstract Image-based identification of circulating tumor cells in microfluidic cytometry condition is one the most challenging perspectives Liquid Biopsy scenario. Here we show a machine learning-powered tomographic phase imaging flow system capable to provide high-throughput 3D phase-contrast tomograms each single cell. In fact, that discrimination against white blood potentially achievable with aid artificial intelligence label-free flow-cyto-tomography method. We propose hierarchical...

10.1038/s41598-023-32110-9 article EN cc-by Scientific Reports 2023-04-13

Abstract The mechanisms underlying genetic susceptibility at loci discovered by genome-wide association study (GWAS) approaches in human cancer remain largely undefined. In this study, we characterized the high-risk neuroblastoma BRCA1-related locus, BARD1, showing that disease-associated variations correlate with increased expression of oncogenically activated isoform, BARD1β. cells, silencing BARD1β showed genotype-specific cytotoxic effects, including decreased substrate-adherence,...

10.1158/0008-5472.can-11-3703 article EN Cancer Research 2012-02-21

Objective Adiponectin is an adipocytokine that exerts beneficial effects on obesity and related disorders by two receptors (ADIPORs). produced as a monomer circulates in serum different oligomers. The oligomerization state the tissue expression of adiponectin ADIPORs are linked to its biological activities. In this study, levels total oligomers were evaluated relation surgical weight loss. was analyzed visceral subcutaneous adipose tissues obese patients. Design methods 25 patients 44 age-...

10.1530/eje-12-1039 article EN European Journal of Endocrinology 2013-04-24

Epigenetic changes in DNA methylation could regulate the expression of several allergy-related genes. We investigated whether tolerance acquisition children with immunoglobulin E (IgE)-mediated cow's milk allergy (CMA) is characterized by a specific profile Th2 (IL-4, IL-5) and Th1 (IL-10, IFN-γ)-associated cytokine genes.DNA CpGs promoting regions genes from peripheral blood mononuclear cells serum level IL-4, IL-5, IL-10 INF-γ were assessed active IgE-mediated CMA (group 1), who acquired...

10.1186/s13148-015-0070-8 article EN cc-by Clinical Epigenetics 2015-03-30

The spectrum of somatic mutation the most aggressive forms neuroblastoma is not completely determined. We sought to identify potential cancer drivers in clinically neuroblastoma.Whole exome sequencing was conducted on 17 germline and tumor DNA samples from high-risk patients with adverse events within 36 months diagnosis (HR-Event3) mutations deep targeted 134 genes selected initial screening additional 48 pairs (62.5% HR-Event3 patients), tumors human-derived cell lines.We revealed 22...

10.18632/oncotarget.8187 article EN Oncotarget 2016-03-18
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