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  1. 原著論文

Regorafenib as a potential adjuvant chemotherapy agent in disseminated small colon cancer: Drug selection outcome of a novel screening system using nanoimprinting 3-dimensional culture with HCT116-RFP cells.

https://repo.qst.go.jp/records/47432
https://repo.qst.go.jp/records/47432
de377b3a-e631-44af-9f37-672f82136001
Item type 学術雑誌論文 / Journal Article(1)
公開日 2016-05-19
タイトル
タイトル Regorafenib as a potential adjuvant chemotherapy agent in disseminated small colon cancer: Drug selection outcome of a novel screening system using nanoimprinting 3-dimensional culture with HCT116-RFP 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 Yoshii, Yukie

× Yoshii, Yukie

WEKO 475082

Yoshii, Yukie

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Furukawa, Takako

× Furukawa, Takako

WEKO 475083

Furukawa, Takako

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Aoyama, Hironori

× Aoyama, Hironori

WEKO 475084

Aoyama, Hironori

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Adachi, Naoya

× Adachi, Naoya

WEKO 475085

Adachi, Naoya

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Zhang, Ming-Rong

× Zhang, Ming-Rong

WEKO 475086

Zhang, Ming-Rong

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Wakizaka, Hidekatsu

× Wakizaka, Hidekatsu

WEKO 475087

Wakizaka, Hidekatsu

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Fujibayashi, Yasuhisa

× Fujibayashi, Yasuhisa

WEKO 475088

Fujibayashi, Yasuhisa

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Saga, Tsuneo

× Saga, Tsuneo

WEKO 475089

Saga, Tsuneo

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吉井 幸恵

× 吉井 幸恵

WEKO 475090

en 吉井 幸恵

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古川 高子

× 古川 高子

WEKO 475091

en 古川 高子

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青山 弥憲

× 青山 弥憲

WEKO 475092

en 青山 弥憲

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足立 直也

× 足立 直也

WEKO 475093

en 足立 直也

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張 明栄

× 張 明栄

WEKO 475094

en 張 明栄

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脇坂 秀克

× 脇坂 秀克

WEKO 475095

en 脇坂 秀克

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藤林 康久

× 藤林 康久

WEKO 475096

en 藤林 康久

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佐賀 恒夫

× 佐賀 恒夫

WEKO 475097

en 佐賀 恒夫

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抄録
内容記述タイプ Abstract
内容記述 Colon cancer is one of the leading causes of cancer death worldwide. Adjuvant chemotherapy following primary surgical treatment is suggested to be beneficial in eradicating invisible disseminated small tumors in colon cancer; however, an effective drug remains to be developed. Recently, we reported a novel drug screening system using a nanoimprinting 3-dimensional (3D) culture that creates multicellular spheroids, which simulate in vivo conditions and, thereby, predict effective drugs in vivo. This study aimed to perform drug selection using our recently developed 3D culture system in a human colon cancer HCT116 cell line stably expressing red fluorescent protein (HCT116-RFP), to determine the most effective agent in a selection of clinically used antitumor agents for colon cancer. In addition, we confirmed the efficacy of the selected drug regorafenib, in vivo using a mouse model of disseminated small tumors. HCT116-RFP cells were cultured using a nanoimprinting 3D culture and in vitro drug selection was performed with 8 clinically used drugs [bevacizumab, capecitabine, cetuximab, 5-fluorouracil (5-FU), irinotecan, oxaliplatin, panitumumab and regorafenib]. An in vivo study was performed in mice bearing HCT116-RFP intraperitoneally disseminated small tumors using 3'-[18F]-fluoro-3'-deoxythymidine-positron emission tomography and fluorescence microscopy imaging to evaluate the therapeutic effects. Regorafenib was determined to be the most effective drug in the 3D culture, and significantly inhibited tumor growth in vivo, compared to the untreated control and 5-FU-treated group. The drug 5-FU is commonly used in colon cancer treatment and was used as a reference. Our results demonstrate that regorafenib is a potentially efficacious adjuvant chemotherapeutic agent for the treatment of disseminated small colon cancer and, therefore, warrants further preclinical and clinical studies.
書誌情報 International journal of oncology

巻 48, 号 4, p. 1477-1484, 発行日 2016-01
出版者
出版者 D.A. Spandidos
ISSN
収録物識別子タイプ ISSN
収録物識別子 1019-6439
PubMed番号
識別子タイプ PMID
関連識別子 26820693
DOI
識別子タイプ DOI
関連識別子 10.3892/ijo.2016.3361
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