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  1. 03 バイオサイエンス
  2. 01 学術雑誌論文

Preclinical evaluation of pentagamavunone-1 as monotherapy and combination therapy for pancreatic cancer in multiple xenograft models

http://hdl.handle.net/10061/0002000124
http://hdl.handle.net/10061/0002000124
7b8a46bc-0588-40bc-8ff8-cfbd0b5f9b0c
アイテムタイプ 学術雑誌論文 / Journal Article(1)
公開日 2024-02-13
タイトル
タイトル Preclinical evaluation of pentagamavunone-1 as monotherapy and combination therapy for pancreatic cancer in multiple xenograft models
言語
言語 eng
資源タイプ
資源タイプ journal article
アクセス権
アクセス権 open access
著者 Kamitani, Naoki

× Kamitani, Naoki

en Kamitani, Naoki

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Nakamae, Ikuko

× Nakamae, Ikuko

en Nakamae, Ikuko

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Yoneda-Kato, Noriko

× Yoneda-Kato, Noriko

en Yoneda-Kato, Noriko

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加藤, 順也

× 加藤, 順也

WEKO 73
e-Rad_Researcher 00273839

ja 加藤, 順也

ja-Kana カトウ, ジュンヤ

en Kato, Jun-ya

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内容記述タイプ Abstract
内容記述 We previously reported that pentagamavunone-1 (PGV-1) effectively inhibited cell proliferation in many types of human tumors, including pancreatic cancer, by inducing M phase (prometaphase) arrest, senescence, and apoptosis with few side effects. However, a detailed evaluation of the effects of PGV-1 on pancreatic cancer cells in an in vivo setting has not yet been conducted. The present study investigated the potential efficacy of PGV-1 as both monotherapy and combination therapy for pancreatic cancer using multiple xenograft mouse assays. A cell-line derived xenograft model (CDX-M) with pancreatic cancer cell line and a patient-derived xenograft mouse model (PDX-M) using resected pancreatic cancer samples without neoadjuvant chemotherapy were established in both heterotopic and orthotopic manners. PGV-1 effectively suppressed tumor formation at the heterotopic and orthotopic sites in CDX-M than in untreated mice. Combination therapy with PGV-1 and gemcitabine more effectively suppressed tumor formation than monotherapy with PGV-1 or gemcitabine when administered after tumor formation. Monotherapy with PGV-1 or gemcitabine less effectively suppressed tumor formation in PDX-M than in CDX-M, whereas combination therapy with PGV-1 and gemcitabine more effectively suppressed tumor formation. PGV-1 as monotherapy and combination therapy with gemcitabine effectively inhibited tumor formation and has potential as an anticancer candidate for pancreatic cancer.
書誌情報 en : Scientific Reports

巻 12, 号 1, 発行日 2022-12-27
出版者
出版者 Nature Research
ISSN
収録物識別子タイプ EISSN
収録物識別子 2045-2322
出版者版DOI
関連タイプ isReplacedBy
識別子タイプ DOI
関連識別子 https://doi.org/10.1038/s41598-022-26863-y
出版者版URI
関連タイプ isReplacedBy
識別子タイプ URI
関連識別子 https://www.nature.com/articles/s41598-022-26863-y
権利
権利情報Resource http://creativecommons.org/licenses/by/4.0/
権利情報 $00A9 The Author(s) 2022 This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
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