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Carbon Ion Beam Combined with Drugs Effectively Destroy Osteosarcoma Cells

https://repo.qst.go.jp/records/77497
https://repo.qst.go.jp/records/77497
9955587b-fb8e-46b3-92da-9a2171360fbc
Item type 会議発表用資料 / Presentation(1)
公開日 2019-11-19
タイトル
タイトル Carbon Ion Beam Combined with Drugs Effectively Destroy 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_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 Sai, Sei

× Sai, Sei

WEKO 805069

Sai, Sei

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Ho Kim, Eun

× Ho Kim, Eun

WEKO 805070

Ho Kim, Eun

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Suzuki, Masao

× Suzuki, Masao

WEKO 805071

Suzuki, Masao

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Fujimori, Akira

× Fujimori, Akira

WEKO 805072

Fujimori, Akira

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Sai, Sei

× Sai, Sei

WEKO 805073

en Sai, Sei

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Ho Kim, Eun

× Ho Kim, Eun

WEKO 805074

en Ho Kim, Eun

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Suzuki, Masao

× Suzuki, Masao

WEKO 805075

en Suzuki, Masao

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Fujimori, Akira

× Fujimori, Akira

WEKO 805076

en Fujimori, Akira

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抄録
内容記述タイプ Abstract
内容記述 We have treated more than 1300 patients with bone and soft tissue tumors including osteosarcoma (OS), and has achieved relatively good outcome. However, the 5-year survival rate is still less than 40%, therefore we need to develop a new combination therapy for further improving treatment results. In this study, we investigate the cell-killing mechanisms by combination of carbon-ion beam and drugs. OS cell lines, KHOS and U2OS were used. Analyses of cell cycle, apoptosis, ERK/AKT signal pathway were performed after carbon-ion beam alone or in combination with osteoporosis treating drug zoledronic acid (ZOL) or anticancer drug cisplatin (CDDP). we found that carbon-ion beam combined with ZOL significantly suppressed OS cell proliferation by arresting cell cycle, inducing apoptosis compared to X-ray or carbon-ion beam alone. In addition, the combination of carbon-ion beam and ZOL inhibited migration as well as invasion of OS cells, induced phosphorylation of MEK, and significantly inhibited ERK/AKT signal pathway related to cell proliferation, as compared with carbon-ion beam, X-ray irradiation or ZOL alone treatment. On the other hand, carbon-ion beam dose-dependently increased induction of apoptosis, and it was further increased when combined with CDDP. In addition, combined treatment with carbon-ion beam and CDDP significantly suppressed Bcl2 gene expression and further suppressed Becli1 or LC3 gene expression as compared to carbon-ion beam, X-ray irradiation alone, or X-ray irradiation and CDDP combination. Taken together, carbon-ion beam in combination with ZOL or CDDP significantly disrupts OS cells compared to carbon-ion beam alone.
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 日本放射線影響学会第62回大会
発表年月日
日付 2019-11-15
日付タイプ Issued
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