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Dual-modality in vivo imaging of electroporation-mediated transgene expression in experimental tumors

https://repo.qst.go.jp/records/69563
https://repo.qst.go.jp/records/69563
44035f26-a5b6-49ec-8178-e318185e2cb3
Item type 会議発表用資料 / Presentation(1)
公開日 2008-10-31
タイトル
タイトル Dual-modality in vivo imaging of electroporation-mediated transgene expression in experimental tumors
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_c94f
資源タイプ conference object
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 U, Winn Aung

× U, Winn Aung

WEKO 682782

U, Winn Aung

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Hasegawa, Sumitaka

× Hasegawa, Sumitaka

WEKO 682783

Hasegawa, Sumitaka

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Koshikawa, Michiko

× Koshikawa, Michiko

WEKO 682784

Koshikawa, Michiko

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Furukawa, Takako

× Furukawa, Takako

WEKO 682785

Furukawa, Takako

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 682786

Saga, Tsuneo

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U Winn Aung

× U Winn Aung

WEKO 682787

en U Winn Aung

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長谷川 純崇

× 長谷川 純崇

WEKO 682788

en 長谷川 純崇

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越川 道子

× 越川 道子

WEKO 682789

en 越川 道子

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古川 高子

× 古川 高子

WEKO 682790

en 古川 高子

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佐賀 恒夫

× 佐賀 恒夫

WEKO 682791

en 佐賀 恒夫

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内容記述タイプ Abstract
内容記述 In vivo electroporation (EP) is one of the efficient methods for effective gene transfer. Application of in vivo EP-mediated gene transfer (EGT) in anticancer gene therapy is highly expected since it could be performed repeatedly, safely and easily with low cost. Meanwhile, effective transfer, long-term expression and non-invasive monitoring are critical for optimal gene therapy. Here we report the feasibility of in vivo optical and MRI of EP-mediated gene expression in tumor model. Initially, we observed the in vivo EGT level and its temporal change by means of optical imaging using red fluorescence protein (RFP) as a reporter gene. Next, we constructed a dual reporter plasmid carrying a gene encoding ferritin heavy chain (FHC), a MRI reporter, and RFP gene to visualize transgene by dual modality. In cellular T2-weighted MRI, cells transfected with FHC plasmid showed lower signal intensity compared to the control cells. Moreover, after in vivo EGT, the plasmid-injected region in the tumor showed low signal intensity on T2-weighted MRI. Thus, our strategy would be a platform technology to evaluate EP-mediated gene therapy without necessity to administer contrast agent or substrate.
会議概要(会議名, 開催地, 会期, 主催者等)
内容記述タイプ Other
内容記述 第67回日本癌学会学術総会
発表年月日
日付 2008-10-30
日付タイプ Issued
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