Decreased Expression of MicroRNA-143 and -145 in Human Gastric Cancers

被引:268
作者
Takagi, Takeshi [1 ,2 ]
Iio, Akio [1 ]
Nakagawa, Yoshihito [1 ]
Naoe, Tomoki [3 ]
Tanigawa, Nobuhiko [2 ]
Akao, Yukihiro [1 ]
机构
[1] Gifu Int Inst Biotechnol, Dept Med Oncol, Kakamigahara, Japan
[2] Osaka Med Coll, Dept Gen & Gastroenterol Surg, Takatsuki, Osaka 569, Japan
[3] Nagoya Univ, Grad Sch Med, Dept Hematol & Oncol, Nagoya, Aichi 4648601, Japan
关键词
MicroRNA-143; MicroRNA-145; Anti-oncomir; Gastric cancer; Insulin receptor substrate-1; beta-Actin; CHRONIC LYMPHOCYTIC-LEUKEMIA; COLON-CANCER; COLORECTAL-CANCER; DOWN-REGULATION; CELLS; GENES; CARCINOMA; GROWTH; IDENTIFICATION; GLIOBLASTOMA;
D O I
10.1159/000218166
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Downregulation of specific microRNAs (miRNAs) occurs in human tumors, which suggests a function for miRNAs in tumor suppression. We investigated the role of the miRNAs miR-143 and miR-145 in gastric cancers. Methods: The expression levels of miR-143 and miR-145 in the samples from 43 patients with gastric cancer were determined by real-time PCR using TaqMan assay. The growth inhibitory effect was estimated by the transfection of human gastric cancer cells with the miRNA. Results: The expression levels of miR-143 and -145 were decreased in most human gastric cancers examined, as previously reported to occur in colon tumors. The transfection of human gastric MKN-1 cells with miR-145 resulted in a greater growth inhibitory effect than that with miR-143, results which were contrary to those in colon cancers. In MKN-1 cells, an additive effect on growth inhibition was shown by the combined transfection with miR-143 and miR-145; further, higher sensitivity to 5-fluorouracil was also observed following the transfection with miR-143 or miR-145. The possible candidate target messenger RNAs of miR-145 were identified to be insulin receptor substrate-1 and beta-actin. Conclusion: Taken together, these findings suggest that miR-143 and miR-145 act as anti-on-comirs common to gastrointestinal tumors. Copyright (C) 2009 S. Karger AG, Basel
引用
收藏
页码:12 / 21
页数:10
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