Development of gene therapy for oral cancer with direct injection of Naked DNA of alpha2-antiplasmin gene
Project/Area Number |
26463044
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Research Category |
Grant-in-Aid for Scientific Research (C)
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Allocation Type | Multi-year Fund |
Section | 一般 |
Research Field |
Surgical dentistry
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Research Institution | Hiroshima University |
Principal Investigator |
HAMANA TOMOAKI 広島大学, 医歯薬保健学研究院(歯), 助教 (40397922)
|
Co-Investigator(Kenkyū-buntansha) |
岡本 哲治 広島大学, 医歯薬保健学研究院(歯), 教授 (00169153)
林堂 安貴 広島大学, 病院(歯), 講師 (70243251)
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Project Period (FY) |
2014-04-01 – 2017-03-31
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Project Status |
Completed (Fiscal Year 2016)
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Budget Amount *help |
¥4,940,000 (Direct Cost: ¥3,800,000、Indirect Cost: ¥1,140,000)
Fiscal Year 2016: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2015: ¥1,430,000 (Direct Cost: ¥1,100,000、Indirect Cost: ¥330,000)
Fiscal Year 2014: ¥2,080,000 (Direct Cost: ¥1,600,000、Indirect Cost: ¥480,000)
|
Keywords | α2-アンチプラスミン / プラスミン / E-カドヘリン / Naked DNA / 口腔癌遺伝子治療 |
Outline of Final Research Achievements |
SCCKN and alpha2-AP transfectants were subcutaneously inoculated into the nude mice. E-cadherin on cell membrane of xenograft from alpha2-AP transfectants was increased compared to SCCKN. Moreover, beta-catenin increased on cell membrane of xenograft from alpha2-AP transfectants. These findings suggest that the suppression of the plasminogen activator/plasmin system by alpha2-AP might reduce the dissemination of OSCC cells. Therefore, it could be expected the development of gene therapy for invasiveness and metastasis of OSCC cells with induction of alpha2-AP into OSCC tissue.
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Report
(4 results)
Research Products
(3 results)
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[Journal Article] Type 2 fibroblast growth factor receptor signaling preserves stemness and prevents differentiation of prostate stem cells from the basal compartment2015
Author(s)
Yanqing Huang, Tomoaki Hamana, Junchen Liu, Cong Wang, Lei An, Pan You, Julia Y. F. Chang, Jianming Xu , Chengliu Jin, Zhongying Zhang, Wallace L. McKeehan, and Fen Wang
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Journal Title
J Biol Chem
Volume: 290
Pages: 17753-61
Related Report
Peer Reviewed
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