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タイトル: Mapping circulating serum miRNAs to their immune-related target mRNAs
著者: Nosirov, Bakhtiyor
Billaud, Joël
Vandenbon, Alexis  kyouindb  KAKEN_id  orcid https://orcid.org/0000-0003-2180-5732 (unconfirmed)
Diez, Diego
Wijaya, Edward
Ishii, Ken J.
Teraguchi, Shunsuke
Standley, Daron M.
キーワード: biomarker
posttranscriptional regulation
random forest
target prediction
発行日: 2017
出版者: Dove Medical Press Ltd.
誌名: Advances and applications in bioinformatics and chemistry : AABC
巻: 10
開始ページ: 1
終了ページ: 9
抄録: Purpose: Evidence suggests that circulating serum microRNAs (miRNAs) might preferentially target immune-related mRNAs. If this were the case, we hypothesized that immune-related mRNAs would have more predicted serum miRNA binding sites than other mRNAs and, reciprocally, that serum miRNAs would have more immune-related mRNA targets than non-serum miRNAs.
Materials and Methods: We developed a consensus target predictor using the random forest framework and calculated the number of predicted miRNA–mRNA interactions in various subsets of miRNAs (serum, non-serum) and mRNAs (immune related, nonimmune related).
Results: Immune-related mRNAs were predicted to be targeted by serum miRNA more than other mRNAs. Moreover, serum miRNAs were predicted to target many more immune-related mRNA targets than non-serum miRNAs; however, these two biases in immune-related mRNAs and serum miRNAs appear to be completely independent.
Conclusion: Immune-related mRNAs have more miRNA binding sites in general, not just for serum miRNAs; likewise, serum miRNAs target many more mRNAs than non-serum miRNAs overall, regardless of whether they are immune related or not. Nevertheless, these two independent phenomena result in a significantly larger number of predicted serum miRNA–immune mRNA interactions than would be expected by chance.
著作権等: This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution - Non Commercial (unported, v3.0) License. By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms.
URI: http://hdl.handle.net/2433/232503
DOI(出版社版): 10.2147/AABC.S121598
PubMed ID: 28203094
出現コレクション:学術雑誌掲載論文等

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