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Intercellular Communication in the Propagation of Bystander Effect and Genomic Instabilty in Human Cells after X-ray, Proton and Carbon

https://repo.qst.go.jp/records/71714
https://repo.qst.go.jp/records/71714
66acb95c-0c0e-41bb-ab0c-ece6a6859c01
Item type 会議発表用資料 / Presentation(1)
公開日 2015-06-09
タイトル
タイトル Intercellular Communication in the Propagation of Bystander Effect and Genomic Instabilty in Human Cells after X-ray, Proton and Carbon
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 Autsavapromporn, Narongchai

× Autsavapromporn, Narongchai

WEKO 705678

Autsavapromporn, Narongchai

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Plante, Ianik

× Plante, Ianik

WEKO 705679

Plante, Ianik

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hua, Liu Cui

× hua, Liu Cui

WEKO 705680

hua, Liu Cui

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Konishi, Teruaki

× Konishi, Teruaki

WEKO 705681

Konishi, Teruaki

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Usami, Noriko

× Usami, Noriko

WEKO 705682

Usami, Noriko

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Funayama, Tomoo

× Funayama, Tomoo

WEKO 705683

Funayama, Tomoo

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Uchihori, Yukio

× Uchihori, Yukio

WEKO 705684

Uchihori, Yukio

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K., Hei Tom

× K., Hei Tom

WEKO 705685

K., Hei Tom

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I, Azzam Edouard

× I, Azzam Edouard

WEKO 705686

I, Azzam Edouard

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Murakami, Takeshi

× Murakami, Takeshi

WEKO 705687

Murakami, Takeshi

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劉 翠華

× 劉 翠華

WEKO 705688

en 劉 翠華

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小西 輝昭

× 小西 輝昭

WEKO 705689

en 小西 輝昭

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内堀 幸夫

× 内堀 幸夫

WEKO 705690

en 内堀 幸夫

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村上 健

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WEKO 705691

en 村上 健

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抄録
内容記述タイプ Abstract
内容記述 Purpose: Radiation-induced bystander effect and genomic instability have important implication in radiotherapy. Their persistence in the progeny may contribute to risk of long-term effect, including cancer. This study investigates the role of gap junction intercellular communication (GJIC) and the quality of radiation in the propagation of stressful effect in bystander cells and their progeny.
\nMaterial and methods: Confluent Human skin fibroblasts were exposed to microbeam irradiations with different linear energy transfer (LET) at mean absorbed dose of 0.4 Gy, in the presence or absence of GJIC inhibitor (AGA) by which 0.036-0.4% of cells were directly targeted by radiation. After 4 h irradiation or following 20 population doublings, the cells were harvested and assayed for micronucleus (MN) formation, gene mutation and protein oxidation.
\nResults: Our results showed that high-LET carbon microbeams (LET ~103 keV/um) and high-LET proton microbeams (LET ~11 keV/um) were more effective than low-LET X ray microbeam (LET ~6 keV/um) in the induction of DNA damage in bystander cells. Interestingly, significant attenuation of MN formation occurred in bystander cells in the presence of AGA after proton and carbon microbeams. In contrast, incubation of the cells with AGA did not significantly affect the induction of MN formation in bystander cells after X irradiation. Further, the progeny of bystander cells exposed to X rays or protons showed persistent oxidative stress which correlated MN formation and mutation frequency. Such effects were not observed after carbon ions. Importantly, the progeny of bystander cells from cultures exposed to protons or carbon ions under conditions where GJIC was inhibited harbored reduced oxidative and genetic damage. This mitigating effect was not detected when the cultured were exposed to X rays. The overall results show the expression of stressful effects in the bystander cells and their progeny are dependent on LET.
\nConclusions: Our findings suggest that the involvement of GJIC-dependent of radiation quality in the propagation of radiation-induced stress to bystander cells and their progeny. In addition, this work provides a strong support to the fact that carbon can significantly reduce the risk of cancer and have potential implications in the therapeutic outcome of radiotherapy.
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 15th International Congress of Radiation Research
発表年月日
日付 2015-05-28
日付タイプ Issued
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