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  1. 30 医学部・医学研究科・保健学研究科
  2. 30b 弘前医学 = Hirosaki Medical Journal
  3. 71巻2-4号

Carbonyl reductase 1-overexpressing exosomes inhibit proliferation of ovarian cancer cells

http://hdl.handle.net/10129/00007248
http://hdl.handle.net/10129/00007248
f30da362-8475-443c-9ae4-e3be8f4016f7
名前 / ファイル ライセンス アクション
Hirosaki Hirosaki Med J 71-2-4_120 (716.8 kB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-03-11
タイトル
タイトル Carbonyl reductase 1-overexpressing exosomes inhibit proliferation of ovarian cancer 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
著者 Takahashi-Ebina, Anna

× Takahashi-Ebina, Anna

Takahashi-Ebina, Anna

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Yokoyama, Minako

× Yokoyama, Minako

Yokoyama, Minako

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Horie, Kayo

× Horie, Kayo

Horie, Kayo

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Yokoyama, Yoshihito

× Yokoyama, Yoshihito

Yokoyama, Yoshihito

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著者所属
値 Department of Obstetrics and Gynecology, Hirosaki University, Graduate School of Medicine
著者所属
値 Department of Obstetrics and Gynecology, Hirosaki University, Graduate School of Medicine
著者所属
値 Department of Bioscience and Laboratory Medicine, Hirosaki University, Graduate School of Health Sciences
著者所属
値 Department of Obstetrics and Gynecology, Hirosaki University, Graduate School of Medicine
抄録
内容記述タイプ Abstract
内容記述 We previously reported that a human carbonyl reductase 1 (CBR1) DNA-dendrimer complex couldpotentially be used in gene therapy for peritoneal metastasis of ovarian cancer. The aims of the current studywere to make exosomes which overexpressed CBR1 and to examine the antiproliferative effect of using the CBR1-overexpressing exosomes on ovarian cancer cells. Endometrial stromal cells (fibroblasts) were transfected withCBR1 DNA by using Lipofectamine, the highest expression level of CBR1 was produced from the cells transfectedunder the condition of Lipofectamin 24 μl/DNA 36 μg for 48 h. Exosomes were purified from culture supernatants byexoEasy Maxi Kit. Western blot showed that CBR1 notably expressed in exosomes extracted from the stromal cellstransfected with CBR1 DNA. Proliferation of ovarian cancer cell line was significantly inhibited by adding CBR1-overexpressing exosomes compared to proliferation of those cells in which exosomes without CBR1 DNA were added.We obtained the evidence that CBR1-overexpressing exosomes could function in carrying CBR1 DNA into ovariancancer cells. Results suggested that exosomes are a useful tool of gene delivery and that a gene therapy of combiningCBR1 DNA and exosomes may be promoted in the treatment of advanced and recurrent ovarian cancers withperitoneal dissemination.
書誌情報 弘前医学

巻 71, 号 2-4, p. 120-130, 発行日 2021-03-05
ISSN
収録物識別子タイプ ISSN
収録物識別子 0439-1721
書誌レコードID
収録物識別子タイプ NCID
収録物識別子 AN00211444
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
出版者
出版者 弘前大学大学院医学研究科
資源タイプ
値 Article
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