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  1. 原著論文

Carbon-ion radiation enhances migration ability and invasiveness of the pancreatic cancer cell, PANC-1, in vitro

https://repo.qst.go.jp/records/47658
https://repo.qst.go.jp/records/47658
0468952d-ce0c-4671-bef2-39cec65745c4
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-03-15
タイトル
タイトル Carbon-ion radiation enhances migration ability and invasiveness of the pancreatic cancer cell, PANC-1, in vitro
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 Fujita, Mayumi

× Fujita, Mayumi

WEKO 478044

Fujita, Mayumi

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Otsuka, Yoshimi

× Otsuka, Yoshimi

WEKO 478045

Otsuka, Yoshimi

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Imadome, Kaori

× Imadome, Kaori

WEKO 478046

Imadome, Kaori

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Endo, Satoshi

× Endo, Satoshi

WEKO 478047

Endo, Satoshi

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Yamada, Shigeru

× Yamada, Shigeru

WEKO 478048

Yamada, Shigeru

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Imai, Takashi

× Imai, Takashi

WEKO 478049

Imai, Takashi

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藤田 真由美

× 藤田 真由美

WEKO 478050

en 藤田 真由美

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荘司 好美

× 荘司 好美

WEKO 478051

en 荘司 好美

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今留 香織

× 今留 香織

WEKO 478052

en 今留 香織

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遠藤 悟史

× 遠藤 悟史

WEKO 478053

en 遠藤 悟史

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山田 滋

× 山田 滋

WEKO 478054

en 山田 滋

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今井 高志

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WEKO 478055

en 今井 高志

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抄録
内容記述タイプ Abstract
内容記述 Pancreatic cancer is an aggressive disease that responds poorly to conventional photon radiotherapy. Carbon-ion (C-ion) radiation has advantages compared with conventional radiotherapy, because it enables more accurate dose distribution and more efficient tumor cell killing. To elucidate the effects of local radiotherapy on the characteristics of metastatic tumors, it is necessary to understand the nature of motility in irradiated tumor cells; this will, in turn, facilitate the development of effective strategies to counter tumor cell motility, which can be used in combination with radiotherapy. The aim of the present study was to examine the invasiveness of pancreatic cancer cells exposed to C-ion irradiation. We found that C-ion irradiation suppressed the migration of MIAPaCa-2, BxPC-3 and AsPC-1; diminished the invasiveness of MIAPaCa-2; and tended to reduce the invasion of BxPC-3 and AsPC-1. However, C-ion irradiation increased the invasiveness of PANC-1 through the activation of plasmin and urokinase-type plasiminogen activator. Administration of serine protease inhibitor (SerPI) alone failed to reduce C-ion-induced PANC-1 invasiveness, whereas the combination of SerPI and Rho-associated coiled-coil forming protein kinase (ROCK) inhibitor suppressed it. Furthermore, PANC-1 showed mesenchymal–amoeboid transition when we treated with SerPI alone. In conclusion, C-ion irradiation is effective in suppressing the invasive potential of several pancreatic tumor cell lines, but not PANC-1; this is the first study showing that C-ion irradiation induces the invasive potential of a tumor cell line. Further in vivo studies are required to examine the therapeutic effectiveness of radiotherapy combined with inhibitors of both mesenchymal and amoeboid modes of tumor cell motility. (Cancer Sci 2012; 103: 677–683)
書誌情報 Cancer Science

巻 103, 号 4, p. 677-683, 発行日 2011-06
ISSN
収録物識別子タイプ ISSN
収録物識別子 1347-9032
DOI
識別子タイプ DOI
関連識別子 10.1111/j.1349-7006.2011.02190.x
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