Paolo G. Arduino

Prof. Paolo G. Arduino

orcid

Research Focus & Metrics

Academic Career Length

23Years (2004-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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26 July 2007 in Journal of Oral Pathology & Medicine
Verified
Journal Article
Closed access
PDF file
PAPaolo G. Arduino
Paolo G. Arduino
SPStephen Porter
Stephen Porter

17 March 2009 in Oral Diseases
Verified
Journal Article
Closed access
PDF file
MCM Carbone
M Carbone
PAPaolo G. Arduino
Paolo G. Arduino
MCM Carrozzo
M Carrozzo
SGS Gandolfo
S Gandolfo
MAM R Argiolas
M R Argiolas
RBR Broccoletti
R Broccoletti

1 November 2010 in The American Journal of Medicine
Verified
Journal Article
Closed access
SFStefano Fedele
Stefano Fedele
SPStephen Porter
Stephen Porter
FDFrancesco D'Aiuto
Francesco D'Aiuto
SASuad Aljohani
Suad Aljohani
PVPaolo Vescovi
Paolo Vescovi
NYNaom Yarom
Naom Yarom

18 April 2018 in BMC Cancer
Verified
Journal Article
Open access
PDF file
CGChiara Gai
Chiara Gai
FCFrancesco Camussi
Francesco Camussi
RBRoberto Broccoletti
Roberto Broccoletti
AGAlessio Gambino
Alessio Gambino
MCMarco Cabras
Marco Cabras
PAPaolo G. Arduino
Paolo G. Arduino
Several studies in the past have investigated the expression of micro RNAs (miRNAs) in saliva as potential biomarkers. Since miRNAs associated with extracellular vesicles (EVs) are known to be protected from enzymatic degradation, we evaluated whether salivary EVs from patients with oral squamous cell carcinoma (OSCC) were enriched with specific subsets of miRNAs. OSCC patients and controls were matched with regards to age, gender and risk factors. Total RNA was extracted from salivary EVs and the differential expression of miRNAs was evaluated by qRT-PCR array and qRT-PCR. The discrimination power of up-regulated miRNAs as biomarkers in OSCC patients versus controls was evaluated by the Receiver Operating Characteristic (ROC) curves. A preliminary qRT-PCR array was performed on samples from 5 OSCC patients and 5 healthy controls whereby a subset of miRNAs were identified that were differentially expressed. On the basis of these results, a cohort of additional 16 patients and 6 controls were analyzed to further confirm the miRNAs that were up-regulated or selectively expressed in the previous pilot study. The following miRNAs: miR-302b-3p and miR-517b-3p were expressed only in EVs from OSCC patients and miR-512-3p and miR-412-3p were up-regulated in salivary EVs from OSCC patients compared to controls with the ROC curve showing a good discrimination power for OSCC diagnosis. The Kyoto Encyclopedia of Gene and Genomes (KEGG) pathway analysis suggested the possible involvement of the miRNAs identified in pathways activated in OSCC. In this work, we suggest that salivary EVs isolated by a simple charge-based precipitation technique can be exploited as a non-invasive source of miRNAs for OSCC diagnosis. Moreover, we have identified a subset of miRNAs selectively enriched in EVs of OSCC patients that could be potential biomarkers.

1 January 2004 in Journal of Investigative Dermatology
Verified
Journal Article
Closed access
MCMarco Carrozzo
Marco Carrozzo
MCMariafederica Uboldi de Capei
Mariafederica Uboldi de Capei
EDEnnia Dametto
Ennia Dametto
MFMaria Edvige Fasano
Maria Edvige Fasano
PAPaolo G. Arduino
Paolo G. Arduino
SGSergio Gandolfo
Sergio Gandolfo

1 March 2006 in International Journal of Oral and Maxillofacial Surgery
Verified
Journal Article
Closed access
FGFilippo Graziani
Filippo Graziani
FDF. D’aiuto
F. D’aiuto
PAPaolo G. Arduino
Paolo G. Arduino
MTM. Tonelli
M. Tonelli
MGM. Gabriele
M. Gabriele