- Author:
Hyun CHANG
1
;
Nayoung KIM
;
Ji Hyun PARK
;
Ryoung Hee NAM
;
Yoon Jeong CHOI
;
Hye Seung LEE
;
Hyuk YOON
;
Cheol Min SHIN
;
Young Soo PARK
;
Jung Min KIM
;
Dong Ho LEE
Author Information
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords: Gastric carcinogenesis; Helicobacter pylori; Microarray; MicroRNAs; TaqMan miRNA assays
- MeSH: Aged; Female; Gene Expression Profiling; *Gene Expression Regulation, Neoplastic; Helicobacter Infections/complications/*genetics; *Helicobacter pylori; Humans; Intestines/metabolism; Male; MicroRNAs/*metabolism; Middle Aged; RNA, Neoplasm/metabolism; Stomach Neoplasms/complications/*genetics
- From:Gut and Liver 2015;9(2):188-196
- CountryRepublic of Korea
- Language:English
- Abstract: BACKGROUND/AIMS: This study was conducted to identify microRNAs (miRNAs) that are differentially expressed in Helicobacter pylori-infected patients with an intestinal type of gastric cancer using miRNA microarray and to confirm the candidate miRNA expression levels. METHODS: Total RNA was extracted from the cancerous and noncancerous regions of formalin-fixed, paraffin-embedded tissues of H. pylori-positive (n=8) or H. pylori-negative (n=8) patients with an intestinal type of gastric cancer. RNA expression was analyzed using a 3,523 miRNA profiling microarray based on the Sanger miRBase. Validation analysis was performed using TaqMan miRNA assays. RESULTS: A total of 219 miRNAs in the aberrant miRNA profiles across the miRNA microarray showed at least a 2-fold change differential expression in H. pylori-positive and H. pylori-negative cancer tissues. After candidate miRNAs were selected using online miRNA databases, TaqMan miRNA assays confirmed that three miRNAs (miR-99b-3p, miR-564, and miR-638) were significantly increased in three H. pylori-positive cancer tissues compared to the H. pylori-negative cancer tissues. Additionally, four miRNAs (miR-204-5p, miR-338-5p, miR-375, and miR-548c-3p) were significantly increased in H. pylori-negative cancer tissues compared to H. pylori-positive cancer tissues. CONCLUSIONS: miRNA expression in the intestinal type of H. pylori infection-dependent gastric cancer suggests that different gastric cancer pathogenesis mechanisms could exist between H. pylori-positive and H. pylori-negative gastric cancer. Additional functional studies are required.

