Expression, function and clinical application of microRNA in oral cancer
Project/Area Number |
24390457
|
Research Category |
Grant-in-Aid for Scientific Research (B)
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Allocation Type | Partial Multi-year Fund |
Section | 一般 |
Research Field |
Surgical dentistry
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Research Institution | Ehime University |
Principal Investigator |
NAKASHIRO Koichi 愛媛大学, 医学(系)研究科(研究院), 准教授 (90314880)
|
Project Period (FY) |
2012-04-01 – 2015-03-31
|
Project Status |
Completed (Fiscal Year 2014)
|
Budget Amount *help |
¥18,460,000 (Direct Cost: ¥14,200,000、Indirect Cost: ¥4,260,000)
Fiscal Year 2014: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2013: ¥4,160,000 (Direct Cost: ¥3,200,000、Indirect Cost: ¥960,000)
Fiscal Year 2012: ¥10,140,000 (Direct Cost: ¥7,800,000、Indirect Cost: ¥2,340,000)
|
Keywords | 口腔癌 / microRNA |
Outline of Final Research Achievements |
In this study, we evaluated the expression of miR-1289 in oral cancer tissues and the growth inhibitory effect of miR-1289 in human oral cancer cells. First, we investigated the expression of miR-1289 in oral cancer tissues by real-time quantitative RT-PCR. The expression levels of miR-1289 were significant decreased in oral cancer tissues compared to adjacent normal oral mucosa tissues. Next, synthetic miR-1289 markedly inhibited the growth of human oral cancer cells in vitro and in vivo. Finally, target genes of miR-1289 were explored by microarray and Ingenuity Pathway Analysis (IPA). Microarray and IPA identified 15 genes as targets of miR-1289. In knockdown of these genes, magnesium transporter 1 (MAGT1) showed the most remarkable cell growth inhibition in human oral cancer cells. These results suggest that miR-1289 functions as a novel tumor suppressive microRNA in oral cancer, and may be a useful therapeutic tool for the patients with oral cancer.
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Report
(4 results)
Research Products
(9 results)
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[Journal Article] Prognostic significance of interleukin-8 and CD163-positive cell-infiltration in tumor tissues in patients with oral squamous cell carcinoma2014
Author(s)
Fujita Y, Okamoto M, Goda H, Tano T, Nakashiro K, Sugita A, Fujita T, Koido S, Homma S, Kawakami Y, Hamakawa H.
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Journal Title
PLoS ONE
Volume: 9
Issue: 12
Pages: e110378-e110378
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] Pathophysiology of lung injury induced by common bile duct ligation in mice2014
Author(s)
Shikata F, Sakaue T, Nakashiro K, Okazaki M, Okamura T, Okura M, Ryugo M, Nakamura Y, Yasugi T, Higashiyama S, Izutani H
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Journal Title
PLoS ONE
Volume: 9
Issue: 4
Pages: e94550-e94550
DOI
Related Report
Peer Reviewed / Open Access
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[Journal Article] Immunochemoradiotherapy for patients with oral squamous cell carcinoma: augmentation of OK-432-induced helper T cell 1 response by 5-FU and X-ray irradiation2013
Author(s)
Tano T, Okamoto M, Kan S, Bando T, Goda H, Nakashiro K, Shimodaira S, Koido S, Homma S, Fujita T, Sato M, Yamashita N, Hamakawa H, Kawakami Y
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Journal Title
Neoplasia
Volume: 15
Pages: 805-814
Related Report
Peer Reviewed
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