2013 Fiscal Year Final Research Report
MicroRNAs and their potential targets associated with characteristics of estrogen receptor-positive breast cancer
Project/Area Number |
24791387
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
General surgery
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Research Institution | Nagoya City University |
Principal Investigator |
ENDO Yumi 名古屋市立大学, 医学(系)研究科(研究院), 助教 (20566228)
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Project Period (FY) |
2012-04-01 – 2014-03-31
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Keywords | マイクロRNA |
Research Abstract |
Recent analyses have identified heterogeneity in ER-positive breast cancer. Subtypes called luminal A and luminal B have been identified, and the tumor characteristics are different in these subtypes. In this study, expression profiles of microRNAs and mRNAs in ER-positive breast cancer tissue were compared between luminal A tumors and luminal B tumors by miRNA and mRNA microarrays. Unsupervised hierarchical clustering analyses revealed distinct expression patterns of miRNAs and mRNAs. We identified a down-regulation of miR-1290 in luminal A tumors. We picked up 11 genes that were potential target genes of the selected miRNAs. Protein expression patterns of the selected target genes were analyzed in ER-positive breast cancer samples by immunohistochemistry: miR-1290 and its 4 putative targets, BCL2, FOXA1, MAPT and NAT1 were identified. Transfection experiments revealed that introduction of miR-1290 into ER-positive breast cancer cells decreased mRNA and protein expression of NAT1.
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[Presentation] Arylamine N-acetyltransferase 1 (NAT1)はmiR-1290 の標的遺伝子であり, 乳癌の予後因子である2014
Author(s)
遠藤友美, 山下啓子, 高橋智, 佐藤慎哉, 吉本信保, 浅野倫子, 波戸ゆかり, 董宇, 藤井義敬, 遠山竜也
Organizer
第114回 日本外科学会学術総会
Place of Presentation
京都
Year and Date
20140403-05
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