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  1. 原著論文

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

https://repo.qst.go.jp/records/49282
https://repo.qst.go.jp/records/49282
57456a49-5bf8-4858-9c0f-d759f0eb1fdd
Item type 学術雑誌論文 / Journal Article(1)
公開日 2018-11-27
タイトル
タイトル Anticancer Effect of Dihydroartemisinin (DHA) in a Pancreatic Tumor Model Evaluated 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_6501
資源タイプ journal article
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 497304

U, Winn Aung

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Sogawa, Chizuru

× Sogawa, Chizuru

WEKO 497305

Sogawa, Chizuru

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Furukawa, Takako

× Furukawa, Takako

WEKO 497306

Furukawa, Takako

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 497307

Saga, Tsuneo

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U Winn Aung

× U Winn Aung

WEKO 497308

en U Winn Aung

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曽川 千鶴

× 曽川 千鶴

WEKO 497309

en 曽川 千鶴

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古川 高子

× 古川 高子

WEKO 497310

en 古川 高子

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佐賀 恒夫

× 佐賀 恒夫

WEKO 497311

en 佐賀 恒夫

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抄録
内容記述タイプ Abstract
内容記述 Background: Dihydroartemisinin (DHA) 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 were evaluated. Materials and Methods: Combined with cell/tumor growth assays, flow cytometric analysis, and Hoechst staining, the effect of DHA was investigated using the pancreatic cancer cell line BxPc3-RFP stably expressing red fluorescence protein and in vitro/in vivo optical imaging. Proteins that regulate proliferation (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 appears to be a complicated process. Optical imaging supports the real-time assessment of DHA efficacy in a preclinical model and comprehensive analysis substantiates that DHA is a potential candidate for pancreatic cancer therapy.
書誌情報 Anticancer Research

巻 31, 号 5, p. 1549-58, 発行日 2011-05
ISSN
収録物識別子タイプ ISSN
収録物識別子 0250-7005
PubMed番号
識別子タイプ PMID
関連識別子 21617209
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