461 PROTON PUMP INHIBITOR AND STATIN USE DECREASE RISK OF ESOPHAGEAL ADENOCARCINOMA AMONG INDIVIDUALS WITH BARRETT'S ESOPHAGUS: A SEER-MEDICARE ANALYSIS

2020 ◽  
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pp. S-87-S-88
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Holli A. Loomans-Kropp ◽  
Matthew Chaloux ◽  
Ellen Richmond ◽  
Asad Umar
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Omran Alsalahi ◽  
...  

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Zhigang Duan ◽  
Aanand D. Naik ◽  
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Hashem B. El-Serag

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2019 ◽  
Vol 9 (1) ◽  
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Deepthi Deconda ◽  
Aihua Li ◽  
Fadlallah Habr ◽  
Weibiao Cao

Abstract Acid reflux may contribute to the progression from Barrett’s esophagus (BE) to esophageal adenocarcinoma (EA). However, it is not clear whether the molecular changes present in BE patients are reversible after proton pump inhibitor (PPI) treatment. In this study we examined whether PPI treatment affects NOX5, microsomal prostaglandin E synthase (mPGES)-1 and inducible nitric oxide synthase (iNOS) expression. We found that NADPH oxidase 5 (NOX5), mPGES-1 and iNOS were significantly increased in BE mucosa. One-month PPI treatment significantly decreased NOX5, mPGES1 and iNOS. In BAR-T cells, NOX5 mRNA and p16 promoter methylation increased after pulsed acid treatment in a time-dependent manner. Four or eight-week-acid induced increase in NOX5 mRNA, NOX5 protein and p16 methylation may be reversible. Twelve-week acid treatment also significantly increased NOX5, mPGES1 and iNOS mRNA expression. However, twelve-week-acid-induced changes only partially restored or did not recover at all after the cells were cultured at pH 7.2 for 8 weeks. We conclude that NOX5, mPGES1 and iNOS may be reversible after PPI treatment. Short-term acid-induced increase in NOX5 expression and p16 methylation might be reversible, whereas long-term acid-induced changes only partially recovered 8 weeks after removal of acid treatment.


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