Chang Hyun, Kim Nayoung, Park Ji Hyun, Nam Ryoung Hee, Choi Yoon Jeong, Lee Hye Seung, Yoon Hyuk, Shin Cheol Min, Park Young Soo, Kim Jung Min, Lee Dong Ho
Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam, Korea.
Department of Internal Medicine, Seoul National University Bundang Hospital, Seongnam and Department of Internal Medicine and Liver Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Gut Liver. 2015 Mar;9(2):188-96. doi: 10.5009/gnl13371.
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.
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.
A total of 219 miRNAs in the aber-rant 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 candi-date 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.
miRNA expression in the intestinal type of H. pylori infection-dependent gastric cancer suggests that different gastric can-cer pathogenesis mechanisms could exist between H. pylori-positive and H. pylori-negative gastric cancer. Additional functional studies are required. (Gut Liver, 2015;9188-196).
背景/目的:本研究旨在利用 miRNA 微阵列鉴定在幽门螺杆菌感染的肠型胃癌患者中差异表达的 microRNA(miRNA),并确认候选 miRNA 的表达水平。
从幽门螺杆菌阳性(n = 8)或幽门螺杆菌阴性(n = 8)的肠型胃癌患者福尔马林固定、石蜡包埋组织的癌组织和非癌组织中提取总 RNA。基于桑格 miRBase 使用 3523 个 miRNA 谱微阵列分析 RNA 表达。使用 TaqMan miRNA 检测进行验证分析。
miRNA 微阵列上异常 miRNA 谱中的总共 219 个 miRNA 在幽门螺杆菌阳性和阴性癌组织中显示出至少 2 倍变化的差异表达。使用在线 miRNA 数据库选择候选 miRNA 后,TaqMan miRNA 检测证实,与幽门螺杆菌阴性癌组织相比,三种 miRNA(miR - 99b - 3p、miR - 564 和 miR - 638)在三个幽门螺杆菌阳性癌组织中显著增加。此外,与幽门螺杆菌阳性癌组织相比,四种 miRNA(miR - 204 - 5p、miR - 338 - 5p、miR - 375 和 miR - 548c - 3p)在幽门螺杆菌阴性癌组织中显著增加。
幽门螺杆菌感染相关的肠型胃癌中的 miRNA 表达表明,幽门螺杆菌阳性和阴性胃癌之间可能存在不同的胃癌发病机制。需要进一步的功能研究。(《胃肠肝脏病学》,2015;9:188 - 196)