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Assessment and Evaluation of the Anticancer Effect of Dihydroartemisinin (DHA) in a Pancreatic Tumor Model by Conventional Methods and Optical Imaging

https://repo.qst.go.jp/records/70530
https://repo.qst.go.jp/records/70530
c5a36f8d-8b30-4506-ae16-93fa22c0c63f
Item type 会議発表用資料 / Presentation(1)
公開日 2011-09-14
タイトル
タイトル Assessment and Evaluation of the Anticancer Effect of Dihydroartemisinin (DHA) in a Pancreatic Tumor Model by Conventional Methods and Optical Imaging
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 692684

U, Winn Aung

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Sogawa, Chizuru

× Sogawa, Chizuru

WEKO 692685

Sogawa, Chizuru

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Furukawa, Takako

× Furukawa, Takako

WEKO 692686

Furukawa, Takako

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 692687

Saga, Tsuneo

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U Winn Aung

× U Winn Aung

WEKO 692688

en U Winn Aung

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曽川 千鶴

× 曽川 千鶴

WEKO 692689

en 曽川 千鶴

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古川 高子

× 古川 高子

WEKO 692690

en 古川 高子

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佐賀 恒夫

× 佐賀 恒夫

WEKO 692691

en 佐賀 恒夫

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抄録
内容記述タイプ Abstract
内容記述 Objective: Dihydroartemisinin (DHA), an active derivative of artemisinin which is now recognized as antimalarial drug, inhibits the growth of certain cancer cells and xenograft tumors. Further understanding of the molecular mechanisms and genetic participants that govern the antineoplastic effects of DHA is necessary. The anticancer effects of DHA and its underlying mechanisms in pancreatic cancer and the efficacy in animal models by noninvasive optical imaging, a suitable technique for real-time characterization of the therapeutic effects on tumor, were evaluated. Materials and Methods: Combined with conventional methods such as cell/tumor growth assays, flow cytometric analysis, and Hoechst staining for apoptosis, the effect of DHA was confirmed using the pancreatic cancer cell line BxPc3-RFP stably expressing red fluorescence protein and in vitro/in vivo optical imaging. Proteins that regulate proliferation (proliferating cell nuclear antigen (PCNA)), apoptosis (Bax and Bcl-2), and angiogenesis (vascular endothelial growth factor (VEGF)) were evaluated in cell and tumor samples by Western blotting and immunohistochemical analyses. Results: DHA inhibited the proliferation and viability of cells in a dose-dependent manner and induced apoptosis. We observed down-regulation of PCNA and Bcl-2, and up-regulation of Bax. VEGF was down-regulated by DHA in cells under normoxic, but not hypoxic, conditions. Fluorescence intensity emitted from cells and tumors correlated linearly with cell count and tumor burden, respectively. Conclusion: DHA inhibits cell and tumor growth by interfering with cell proliferation and inducing apoptosis. The antiangiogenic effect of DHA may be partial and appears to be a complicated process. Optical imaging allows convenient and reliable real-time evaluation of DHA efficacy in a preclinical model and comprehensive analysis substantiates that DHA is a potential candidate for pancreatic cancer therapy.
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 2011 World Molecular Imaging Congress (WMIC)
発表年月日
日付 2011-09-10
日付タイプ Issued
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