Pilot study identifying circulating miRNA signature specific to alcoholic chronic pancreatitis and its implication on alcohol?mediated pancreatic tissue injury

ABSTRACT: Abstract

Background and Aim

Alcohol exerts its effects on organs in multiple ways. Alcoholic chronic pancreatitis (ACP) is a disease in which alcohol triggers the pathological changes in pancreas, leading to chronic inflammation and fibrosis. The molecular mechanism behind these changes is not clear. Identification of key circulating miRNA changes in ACP patients and determination of the fraction that is secreted from diseased pancreas not only could serve as potential biomarker for assessing disease severity, but also could help identifying the molecular alterations prevailing in the organ precipitating the disease, to some extent.

Methods

We performed microRNA microarray using the Affymetrix miRNA 4.0 platform to identify differentially expressed miRNAs in serum of ACP patients as compared to alcoholic control individuals and then found out how many of them could be pancreas?specific and exosomally secreted. We further analyzed a pancreatitis?specific gene expression data set to find out the differentially expressed genes in diseased pancreas and explored the possible role of those selected miRNAs in regulation of gene expression in ACP.

Results

We identified 14 miRNAs differentially expressed in both serum and pancreas and also identified their experimentally validated targets. Transcription factors modulating the miRNA expression in an alcohol?dependent manner were also identified and characterized to derive the miRNA–gene–TF interaction network responsible for progression of the disease.

Conclusions

Differentially expressed miRNA signature demonstrated significant changes in both pro? and anti?inflammatory pathways probably balancing the chronic inflammation in the pancreas. Our findings also suggested possible involvement of pancreatic stellate cells in disease progression. We aimed at integrating the miRNA profiling and gene expression results to understand molecular basis of alcohol mediated injury of pancreas. Our approach is first ever such attempt identifying pro? and anti?inflammatory pathways contributing to pancreatic inflammation and fibrosis, possibly modulating pancreatic stellate cell function.

SUBMITTER: Chhatriya B 

PROVIDER: S-EPMC7731805 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature