Over- and under-expressed microRNAs in human colorectal cancer

被引:339
作者
Motoyama, Kazuo [2 ,3 ]
Inoue, Hiroshi [2 ]
Takatsuno, Yasushi [2 ,3 ]
Tanaka, Fumiaki [2 ]
Mimori, Koshi [2 ]
Uetake, Hiroyuki [3 ]
Sugihara, Kenichi [3 ]
Mori, Masaki [1 ,2 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Surg Gastroenterol, Suita, Osaka 5650871, Japan
[2] Kyushu Univ, Med Inst Bioregulat, Dept Mol & Surg Oncol, Beppu, Oita 8740838, Japan
[3] Tokyo Med & Dent Univ, Grad Sch Med & Dent Sci, Dept Surg Oncol, Bunkyo Ku, Tokyo 1138519, Japan
基金
日本科学技术振兴机构;
关键词
microRNA; human colorectal cancer; microRNA microarray; LUNG CANCERS; IDENTIFICATION; GENES; ONCOMIRS; CLUSTER;
D O I
10.3892/ijo_00000233
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
MicroRNAs (miRNAs) constitute a class of small (21-23 nucleotides) noncoding RNAs that function as post-transcriptional gene regulators. It is becoming increasingly clear that altered miRNA expression correlates with the pathogenesis of cancers. The purpose of this study was to determine the up-regulated miRNAs in human colorectal cancer. Total RNA was isolated from cancer tissues and corresponding noncancerous tissues from surgically resected colorectal cancers. The expression profiles of miRNAs were determined using a miRNA microarray containing 455 human miRNA probes. The expression status of selected miRNAs in paired clinical samples was then investigated by real-time RT-PCR. Twenty-one miRNAs were identified by miRNA array analysis as overexpressed in colorectal cancer tissues compared to normal epithelial tissues. Among them, the expression of miR-31, miR-183, miR-17-5p, miR-18a, miR-20a and miR-92 were confirmed to be significantly higher in cancer tissues than in normal tissues (P<0.05). In contrast, the expression of miR-143 and miR-145 in cancer tissues were significantly lower than in normal tissues (P<0.05). The miR-18a overexpression group tended to have a poorer clinical prognosis than the low expression group (P=0.07). We identified miRNAs that were overexpressed or underexpressed in colorectal cancers and which may be correlated with colorectal carcinogenesis.
引用
收藏
页码:1069 / 1075
页数:7
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