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December 03-04, 2018 | Chicago, USA
American Pathology and Oncology Research
&
15
th
International Congress on
Microbial Genetics and Molecular Microbiology
International Conference on
Journal of Clinical & Experimental Pathology | ISSN: 2161-0681 | Volume 8
Weibiao Cao
Rhode Island Hospital and Brown University, USA
Mechanisms of the progression from Barrett’s esophagus to esophageal adenocarcinoma: Role of NADPH
oxidase NOX5-S
E
sophageal adenocarcinoma (EA) has increased in incidence over the past several decades and is characterized by a poor
prognosis. Gastroesophageal reflux disease (GERD) complicated by Barrett’s esophagus (BE) is a major risk factor for the
development of EA. There is a progression from BE to dysplasia and to EA. However, the mechanisms of progression from BE
to EA are not fully understood. We found that NOX5-S is present in Barrett’s cells BAR-T and EA cells FLO and OE33 and is
overexpressed in FLO cells and EA tissues. NOX5-S mRNA is also increased in Barrett’s mucosa with high-grade dysplasia.
Pulsed acid treatment significantly increases NOX5-S expression and H
2
O
2
production in BAR-T and OE33 cells and Barrett’s
mucosa. These data suggest that NOX5-S may be a source of overproduction of reactive oxygen species (ROS) in BE and in
EA cells. We also found that acid-induced increase in NOX5-S expression may depend on activation of Rho kinase, ERK1/2
MAP kinases, and cAMP response element-binding protein. The acid may also induce production of platelet-activating factor,
which activates signal transducer and activator of transcription 5 (STAT5) and then upregulates NOX5-S. In addition, NOX5-S
mediates an acid-induced increase in cell proliferation in Barrett’s cells BAR-T and EA cells (OE33 and FLO). NOX5-S-mediated
increase in cell proliferation may depend on the activation of COX2 and microsomal prostaglandin E synthase 1 (mPGES1), and
downregulation of p16 via promoter methylation. NOX5-S also mediates acid-induced DNA damage. These data suggest that
persistent acid reflux present in BE patients may upregulate NOX5-S, increase production of ROS and cell proliferation, and cause
DNA damage, thereby contributing to the progression from BE to dysplasia and to EA.
Biography
Weibiao Cao obtained his MD degree from Zhejiang Medical University in Hangzhou, China in 1986. He worked as a Research Associate and an Assistant Professor in
Division of Gastroenterology, Rhode Island Hospital, RI, the USA from 1996 to 2007. He was trained as a Pathology Resident from 2007 to 2011 and a GI pathology fellow
from 2011 to 2012 in the Department of Pathology, Rhode Island Hospital and Brown University, USA. He has been an attending pathologist since 2012, an Associate
Professor since 2013 and a Director of the autopsy service since 2017 in Department of Pathology, Rhode Island Hospital and Brown University, USA. He has been a
Member of Oncology C (ONCC) Scientific Peer Review panel, Department of Veterans Affairs, USA and an Editorial Board Member of Scientific Reports (impact factor
4.26) since 2015.
weibiao_cao@brown.eduWeibiao Cao, J Clin Exp Pathol 2018, Volume 8
DOI: 10.4172/2161-0681-C5-056