Systematic Analysis of miRNA Regulations in Tumor Cells

博士 === 國立交通大學 === 生物資訊研究所 === 97 === MicroRNAs (miRNAs) are small non-coding RNA molecules of ~22 nt sequences that have an important role in the translational inhibition and degradation of mRNA to downregulate gene expression. Recent work supports miRNAs downregulate gene expression during various...

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Main Authors: Hsu, Paul Wei-Che, 徐唯哲
Other Authors: Huang, Hsien-Da
Format: Others
Language:en_US
Online Access:http://ndltd.ncl.edu.tw/handle/51573551973191605885
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spelling ndltd-TW-097NCTU51120042015-10-13T14:53:17Z http://ndltd.ncl.edu.tw/handle/51573551973191605885 Systematic Analysis of miRNA Regulations in Tumor Cells 分析腫瘤細胞中微小核醣核酸的調控機制 Hsu, Paul Wei-Che 徐唯哲 博士 國立交通大學 生物資訊研究所 97 MicroRNAs (miRNAs) are small non-coding RNA molecules of ~22 nt sequences that have an important role in the translational inhibition and degradation of mRNA to downregulate gene expression. Recent work supports miRNAs downregulate gene expression during various crucial cell processes such as apoptosis, differentiation and development. Recent studies have suggested that oncogenesis may be link with aberrant expression of miRNAs, but in most case it is still not clear what mechanism of miRNA leads to cancer formation. In this study, we analyzed more than 200 miRNAs which are aberrantly expressed in tumor cells, and the tissue specificity is tested by the miRNA expression among normal tissues. We identified 20 oncomirs which are up or down-expressed to regulate downstream genes and involved in oncogenesis of eight cancer types. We also predicted the transcription factor binding sites (TFBS) in miRNA promoter and identified miRNA targets which are tumour suppressors or oncogenes. Those analyses are integrated for miRNA regulatory network construction in eight cancers, and we hope our achievements can support cancer research and clinical trial. Huang, Hsien-Da 黃憲達 學位論文 ; thesis 125 en_US
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description 博士 === 國立交通大學 === 生物資訊研究所 === 97 === MicroRNAs (miRNAs) are small non-coding RNA molecules of ~22 nt sequences that have an important role in the translational inhibition and degradation of mRNA to downregulate gene expression. Recent work supports miRNAs downregulate gene expression during various crucial cell processes such as apoptosis, differentiation and development. Recent studies have suggested that oncogenesis may be link with aberrant expression of miRNAs, but in most case it is still not clear what mechanism of miRNA leads to cancer formation. In this study, we analyzed more than 200 miRNAs which are aberrantly expressed in tumor cells, and the tissue specificity is tested by the miRNA expression among normal tissues. We identified 20 oncomirs which are up or down-expressed to regulate downstream genes and involved in oncogenesis of eight cancer types. We also predicted the transcription factor binding sites (TFBS) in miRNA promoter and identified miRNA targets which are tumour suppressors or oncogenes. Those analyses are integrated for miRNA regulatory network construction in eight cancers, and we hope our achievements can support cancer research and clinical trial.
author2 Huang, Hsien-Da
author_facet Huang, Hsien-Da
Hsu, Paul Wei-Che
徐唯哲
author Hsu, Paul Wei-Che
徐唯哲
spellingShingle Hsu, Paul Wei-Che
徐唯哲
Systematic Analysis of miRNA Regulations in Tumor Cells
author_sort Hsu, Paul Wei-Che
title Systematic Analysis of miRNA Regulations in Tumor Cells
title_short Systematic Analysis of miRNA Regulations in Tumor Cells
title_full Systematic Analysis of miRNA Regulations in Tumor Cells
title_fullStr Systematic Analysis of miRNA Regulations in Tumor Cells
title_full_unstemmed Systematic Analysis of miRNA Regulations in Tumor Cells
title_sort systematic analysis of mirna regulations in tumor cells
url http://ndltd.ncl.edu.tw/handle/51573551973191605885
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