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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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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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.
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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 |
work_keys_str_mv |
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