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Down regulation of ZDHHC8 enhances radiosensitivity of human mesothelioma in vitro and in vivo

https://repo.qst.go.jp/records/70509
https://repo.qst.go.jp/records/70509
75874598-eef8-4938-9a33-60d22cf78235
Item type 会議発表用資料 / Presentation(1)
公開日 2011-09-06
タイトル
タイトル Down regulation of ZDHHC8 enhances radiosensitivity of human mesothelioma in vitro and in vivo
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 Sudou, Hitomi

× Sudou, Hitomi

WEKO 692405

Sudou, Hitomi

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Tsuji, Atsushi

× Tsuji, Atsushi

WEKO 692406

Tsuji, Atsushi

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Sugyou, Aya

× Sugyou, Aya

WEKO 692407

Sugyou, Aya

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Ogawa, Yuriko

× Ogawa, Yuriko

WEKO 692408

Ogawa, Yuriko

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Sagara, Masashi

× Sagara, Masashi

WEKO 692409

Sagara, Masashi

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 692410

Saga, Tsuneo

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須藤 仁美

× 須藤 仁美

WEKO 692411

en 須藤 仁美

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辻 厚至

× 辻 厚至

WEKO 692412

en 辻 厚至

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須尭 綾

× 須尭 綾

WEKO 692413

en 須尭 綾

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小川 由利子

× 小川 由利子

WEKO 692414

en 小川 由利子

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相良 雅史

× 相良 雅史

WEKO 692415

en 相良 雅史

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佐賀 恒夫

× 佐賀 恒夫

WEKO 692416

en 佐賀 恒夫

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内容記述タイプ Abstract
内容記述 Malignant mesothelioma is highly lethal and the prognosis following therapy is very poor. The effect of radiation monotherapy for mesothelioma is reported to be minimal. To improve the efficacy of radiotherapy, a novel molecular-targeted radiosensitizing agent is needed to increase radiosensitivity of mesothelioma cells. We have previously identified ZDHHC8 as a novel radiation susceptibility gene based on the functional screening in human cells. In this study, we analyzed the effect of ZDHHC8 knockdown with radiation on mesothelioma cells and assessed the therapeutic efficacy in mouse model. In mesothelioma cells, knockdown of ZDHHC8 by siRNA significantly reduced cell survival after irradiation, induced the impairment of G2/M checkpoint, and increased the frequency of cells with micronuclei and apoptosis. In the mouse model, the treatment with ZDHHC8 siRNA and irradiation significantly suppressed tumor growth and increased apoptosis, whereas ZDHHC8 siRNA alone did not. These results suggest that ZDHHC8 knockdown with X-irradiation induced chromosomal instability and cell death including apoptosis through the defects of G2/M checkpoint, and the combination of ZDHHC8 depletion and irradiation has the potential to be effective therapy for malignant mesothelioma.
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 14th International Congress of Radiation Research(ICRR’2011)
発表年月日
日付 2011-09-01
日付タイプ Issued
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