https://scholars.lib.ntu.edu.tw/handle/123456789/378174
標題: | Quantitative proteomics reveals diverse roles of mir-148a from gastric cancer progression to neurological development | 作者: | Hu, C.-W. Tseng, C.-W. Chien, C.-W. Huang, H.-C. Ku, W.-C. Lee, S.-J. Chen, Y.-J. Juan, H.-F. |
關鍵字: | iTRAQ; miR-148a; neurological development; proteome; zebrafish | 公開日期: | 2013 | 出版社: | American Chemical Society | 卷: | 12 | 期: | 9 | 起(迄)頁: | 3993-4004 | 來源出版物: | Journal of Proteome Research | 摘要: | MicroRNAs (miRNAs) are noncoding RNAs that control gene expression either by degradation of mRNAs or inhibition of protein translation. miR-148a has been reported to have the impacts on tumor progression. Here, a quantitative proteomics combined with stable isotope labeling was applied to identify the global profile of miR-148a-regulated downstream proteins. The data have been deposited to the ProteomeXchange with identifier PXD000190. A total of 2938 proteins were quantified, and 55 proteins were considered to be regulated by miR-148a. We found that not only proteins associated with cancer progression but also molecules involved in neural development were regulated by miR-148a. This study is the first to identify the function of miR-148a in neural development by using a proteomic approach. Analysis of a public clinical database also showed that the patients with neural diseases could display abnormal expression of miR-148a. Moreover, silencing of miR-148a led to the abnormal morphology and decreased expression of neuron-related markers in the developing brain of zebrafish. These results provided important insight into the regulation of neurological development elicited by miR-148a. ? 2013 American Chemical Society. |
URI: | http://www.scopus.com/inward/record.url?eid=2-s2.0-84883769174&partnerID=MN8TOARS http://scholars.lib.ntu.edu.tw/handle/123456789/378174 |
DOI: | 10.1021/pr400302w | SDG/關鍵字: | microRNA; microRNA 148a; stable isotope; unclassified drug; animal model; article; cancer growth; cell line; chromatography; controlled study; DNA degradation; DNA flanking region; embryo; gene control; gene expression; gene function; gene silencing; genetic transfection; human; human cell; in vivo study; morphology; nervous system development; neurologic disease; nonhuman; priority journal; protein synthesis; proteomics; stomach cancer; tumor growth; wild type; zebra fish; Alzheimer Disease; Animals; Base Sequence; Brain; Case-Control Studies; Cell Line, Tumor; Disease Progression; Gene Expression Regulation, Neoplastic; Humans; MicroRNAs; Parkinson Disease; Proteomics; RNA Interference; Sequence Homology, Nucleic Acid; Spinal Cord; Stomach Neoplasms; Transcriptome; Zebrafish |
顯示於: | 生命科學系 |
在 IR 系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。