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  1. 原著論文

Carbon-Ion Beam Irradiation Alone or in Combination with Zoledronic Acid Effectively Kills Osteosarcoma Cells.

https://repo.qst.go.jp/records/79563
https://repo.qst.go.jp/records/79563
e8a34907-4b4a-4d0a-b611-a20c0995c687
Item type 学術雑誌論文 / Journal Article(1)
公開日 2020-03-18
タイトル
タイトル Carbon-Ion Beam Irradiation Alone or in Combination with Zoledronic Acid Effectively Kills Osteosarcoma Cells.
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 Ho Kim, Eun

× Ho Kim, Eun

WEKO 1007607

Ho Kim, Eun

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Mi-Sook, Kim

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WEKO 1007608

Mi-Sook, Kim

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Takahashi, Akihisa

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WEKO 1007609

Takahashi, Akihisa

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Suzuki, Masao

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WEKO 1007610

Suzuki, Masao

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Vares, Guillaume

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WEKO 1007611

Vares, Guillaume

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Uzawa, Akiko

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WEKO 1007612

Uzawa, Akiko

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Fujimori, Akira

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WEKO 1007613

Fujimori, Akira

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Ohno, Tatsuya

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WEKO 1007614

Ohno, Tatsuya

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Sai, Sei

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WEKO 1007615

Sai, Sei

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Ho Kim, Eun

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WEKO 1007616

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Akihisa, Takahashi

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WEKO 1007617

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Masao, Suzuki

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WEKO 1007618

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Vares, Guillaume

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WEKO 1007619

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Akiko, Uzawa

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WEKO 1007620

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Akira, Fujimori

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WEKO 1007621

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Tatsuya, Ohno

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WEKO 1007622

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Sei, Sai

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WEKO 1007623

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抄録
内容記述タイプ Abstract
内容記述 Osteosarcoma (OSA) is the most common malignant bone tumor in children and adolescents. The overall five-year survival rate for all bone cancers is below 70%; however, when the cancer has spread beyond the bone, it is about 15–30%. Herein, we evaluated the effects of carbon-ion beam irradiation alone or in combination with zoledronic acid (ZOL) on OSA cells. Carbon-ion beam irradiation in combination with ZOL significantly inhibited OSA cell proliferation by arresting cell cycle progression and initiating KHOS and U2OS cell apoptosis, compared to treatments with carbon-ion beam irradiation, X-ray irradiation, and ZOL alone. Moreover, we observed that this combination greatly inhibited OSA cell motility and invasion, accompanied by the suppression of the Pi3K/Akt and MAPK signaling pathways, which are related to cell proliferation and survival, compared to individual treatments with carbon-ion beam or X-ray irradiation, or ZOL. Furthermore, ZOL treatment upregulated microRNA (miR)-29b expression; the combination with a miR-29b mimic further decreased OSA cell viability via activation of the caspase 3 pathway. Thus, ZOL-mediated enhancement of carbon-ion beam radiosensitivity may occur via miR-29b upregulation; co-treatment with the miR-29b mimic further decreased OSA cell survival. These findings suggest that the carbon-ion beam irradiation in combination with ZOL has high potential to increase OSA cell death.
書誌情報 Cancers

巻 12, 号 3, p. 698, 発行日 2020-03
出版者
出版者 MDPI
ISSN
収録物識別子タイプ ISSN
収録物識別子 2072-669
DOI
識別子タイプ DOI
関連識別子 10.3390/cancers12030698
関連サイト
識別子タイプ URI
関連識別子 https://www.mdpi.com/2072-6694/12/3/698
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