Comprehensive Analysis of Serum microRNAs in Autoimmune Pancreatitis

被引:19
作者
Hamada, Shin [1 ]
Masamune, Atsushi [1 ]
Kanno, Atsushi [1 ]
Shimosegawa, Tooru [1 ]
机构
[1] Tohoku Univ, Grad Sch Med, Div Gastroenterol, Sendai, Miyagi 9808574, Japan
基金
日本学术振兴会;
关键词
IgG4-related disease; Biomarker; Ingenuity pathway analysis; Microarray; Pancreatic cancer; Pancreatitis; STELLATE CELLS; CANCER CELLS; DIAGNOSTIC-CRITERIA; EXPRESSION; MIR-150; CYTOKINES; BIOMARKER; CONSENSUS; INCREASE; DISEASES;
D O I
10.1159/000381283
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background/Aims: Autoimmune pancreatitis (AIP) is a rare disease that has recently emerged as a unique type of pancreatitis with a presumed autoimmune etiology. MicroRNA (miRNA) is a small non-coding RNA that targets multiple mRNAs. miRNAs might exist in serum in a stabilized form, suggesting its potential application as a biomarker. We here examined the miRNA expression profile in the serum of patients with AIP. Methods: miRNAs were prepared from serum samples of patients with various pancreatic diseases (AIP (n = 3, each before and after the steroid therapy), chronic pancreatitis (n = 5), pancreatic cancer (n = 5)) or healthy controls (n = 5). A human miRNA Oligo chip containing approximately 2,000 miRNAs was used to identify differentially expressed miRNAs. Ingenuity Pathway Analysis (IPA) was used for the integrated analysis of altered miRNAs. Results: Microarray analysis identified miRNAs highly expressed in the serum of patients with AIP: 13 miRNAs vs. CP, 204 miRNAs vs. pancreatic cancer, and 19 miRNAs vs. healthy controls. miR-150-5p was commonly upregulated in AIP compared to the other samples. IPA revealed the most biological processes affected by the steroid therapy including cellular development, cellular growth, and cell movement. Conclusion: Our results identified that miRNAs were differentially expressed in the serum of AIP patients. (C) 2015 S. Karger AG, Basel
引用
收藏
页码:263 / 271
页数:9
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