MicroRNA Expression and Functional Profiles of Osteosarcoma

被引:30
作者
Kobayashi, Eisuke [1 ,2 ]
Satow, Reiko [1 ]
Ono, Masaya [1 ]
Masuda, Mari [1 ]
Honda, Kazufumi [1 ]
Sakuma, Tornohiro [3 ]
Kawai, Akira [4 ]
Morioka, Hideo [2 ]
Toyama, Yoshiaki [2 ]
Yamada, Tesshi [1 ]
机构
[1] Keio Univ, Natl Canc Ctr Res Inst, Div Chemotherapy & Clin Res, Tokyo, Japan
[2] Keio Univ, Dept Orthoped Surg, Tokyo, Japan
[3] Mitsui Knowledge Ind, BioBusiness Grp, Tokyo, Japan
[4] Natl Canc Ctr, Musculoskeleta Oncol Div, Tokyo, Japan
关键词
MicroRNA; Osteosarcoma; Microarray; Proteomics; LIQUID-CHROMATOGRAPHY; PROGNOSTIC-FACTORS; BETA-CATENIN; CANCER; LET-7; MECHANISM; CHEMORESISTANCE; IDENTIFICATION; PREDICTION; PROTEOMICS;
D O I
10.1159/000357408
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objective: Osteosarcoma (OS) is the most frequent primary malignant bone tumor in children and young adults. Although the introduction of combined neoadjuvant chemotherapy has significantly prolonged survival, the outcome for OS patients showing a poor response to chemotherapy is still unfavorable. In order to develop new therapeutic approaches, elucidation of the entire molecular pathway regulating OS cell proliferation would be desirable. Methods: MicroRNA (miRNA) are highly conserved noncoding RNA that play important roles in the development and progression of various other cancers. Using miRNA microarrays capable of detecting a known number of 933 miRNA, 108 miRNA were found to be commonly expressed in 24 samples of OS tissue and subjected to a cell proliferation assay. Results: We found that inhibition of 5 let-7 family nniRNA (hsa-let-7a, b, f, g and i) significantly suppressed the proliferation of OS cells. Using a quantitative shotgun proteomics approach, we also found that the let-7 family miRNA regulated the expression of vimentin and serpin H1 proteins. Conclusions: Our present results indicate the involvement of let-7 family miRNA in regulation of the cell proliferation as well as epithelial-mesenchymal transition of OS. Thus, let-7 family miRNA may potentially provide novel targets for the development of therapeutic strategies against OS. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:94 / 103
页数:10
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