2011 Fiscal Year Final Research Report
Estrogen receptor knock down therapy using microRNA for breast cancer patients
Project/Area Number |
21591674
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Single-year Grants |
Section | 一般 |
Research Field |
General surgery
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Research Institution | Nagoya City University |
Principal Investigator |
TOYAMA Tatsuya 名古屋市立大学, 大学院・医学研究科, 准教授 (30315882)
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Co-Investigator(Kenkyū-buntansha) |
YAMASHITA Hiroko 名古屋市立大学, 大学院・医学研究科, 准教授 (70332947)
SUGIURA Hiroshi 名古屋市立大学, 大学院・医学研究科, 研究員 (20381882)
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Project Period (FY) |
2009 – 2011
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Keywords | 乳癌 / マイクロRNA / エストロゲン・レセプター |
Research Abstract |
Several microRNAs(miRNAs) that directly target ERα have been identified. In this study, expression levels of miRNAs that directly target ERα, including miR-18a, miR-18b, miR-22, miR-193b, miR-206, miR-221/222 and miR-302c, were analyzed in human breast cancer samples by quantitative reverse transcription-PCR analysis. Correlations between the expression levels of these miRNAs and clinicopathological factors were analyzed. miR-18a expression was much higher in ERα-negative than in ERα-positive tumors, with the expression levels of miR-18a not differing in ERα-positive breast cancer as a function of ERαprotein level. Surprisingly, the expression levels of miR-193b and miR-221 were significantly lower in ERα-negative than in ERα-positive tumors, and the levels of these miRNAs gradually increased as ERα protein expression increased. Our results suggest that miR-206 could be a novel candidate for endocrine therapy that targets only ERα in breast cancer.
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[Presentation] Low Expression of microRNA-210 Is an Independent Good Prognostic Factor in Japanese Triple-Negative Breast Cancer Patients2011
Author(s)
Toyama T, Kondo N, Endo Y, Sugiura H, Yoshimoto N, Iwasa M, Takahashi S, Iwase H, Fujii Y, Yamashita H
Organizer
34rd Annual San Antonio Breast Cancer Symposium
Place of Presentation
San Antonio, USA
Year and Date
20111206-10
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