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Analysis of underlying mechanisms for combination therapy of carbon-ion irradiation and dendritic cell immunotherapy.

https://repo.qst.go.jp/records/71285
https://repo.qst.go.jp/records/71285
aaee98d6-52cf-42bf-8ce4-bdb2668c8410
Item type 会議発表用資料 / Presentation(1)
公開日 2013-10-10
タイトル
タイトル Analysis of underlying mechanisms for combination therapy of carbon-ion irradiation and dendritic cell immunotherapy.
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 Shimokawa, Takashi

× Shimokawa, Takashi

WEKO 700796

Shimokawa, Takashi

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Fujita, Hidetoshi

× Fujita, Hidetoshi

WEKO 700797

Fujita, Hidetoshi

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Hosoi, Akihiro

× Hosoi, Akihiro

WEKO 700798

Hosoi, Akihiro

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Sato, Katsutoshi

× Sato, Katsutoshi

WEKO 700799

Sato, Katsutoshi

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Kakimi, Kazuhiro

× Kakimi, Kazuhiro

WEKO 700800

Kakimi, Kazuhiro

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Imai, Takashi

× Imai, Takashi

WEKO 700801

Imai, Takashi

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下川 卓志

× 下川 卓志

WEKO 700802

en 下川 卓志

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藤田 英俊

× 藤田 英俊

WEKO 700803

en 藤田 英俊

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佐藤 克俊

× 佐藤 克俊

WEKO 700804

en 佐藤 克俊

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今井 高志

× 今井 高志

WEKO 700805

en 今井 高志

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抄録
内容記述タイプ Abstract
内容記述 Carbon-ion (C-ion) radiotherapy (RT) is an advanced RT effective in tumors that are resistant to conventional RT due to its biological properties and excellent dose distribution. However, metastasis control is an important issue to improve C-ion RT.
We previously reported that the combination of C-ion irradiation with dendritic cell (DC) immunotherapy significantly suppressed lung metastases in murine models, such as NRS1 mouse squamous cell carcinoma cell transplanted C3H/He mouse. However, the underlying mechanisms are still not clearly understood. In this study, we aim to clarify the impact of C-ion irradiation on the combination therapy in terms of immature DC (iDC) activation. To investigate the effect of C-ion irradiation on DC immunotherapy, we examined whether irradiated or non-irradiated cancer cells can activate immature DC cells by co-culture. NRS1 cells were irradiated with C-ion, then co-cultured for three days with iDCs, which were isolated from C3H/He mice. Activation of the DC was evaluated by a flow cytometer and real-time qPCR. It clearly showed that iDCs were effectively activated by C-ion irradiated cancer cells, but not by non-irradiated cancer cells.
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 The 72nd Annual Meeting of the Japanese Cancer Association
発表年月日
日付 2013-10-05
日付タイプ Issued
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