このアイテムのアクセス数: 195

このアイテムのファイル:
ファイル 記述 サイズフォーマット 
s41598-018-27138-1.pdf2.12 MBAdobe PDF見る/開く
完全メタデータレコード
DCフィールド言語
dc.contributor.authorSuzuki, Yusukeen
dc.contributor.authorIi, Masaakien
dc.contributor.authorSaito, Takashien
dc.contributor.authorTerai, Yoshitoen
dc.contributor.authorTabata, Yasuhikoen
dc.contributor.authorOhmichi, Masahideen
dc.contributor.authorAsahi, Michioen
dc.contributor.alternative田畑, 泰彦ja
dc.date.accessioned2018-12-14T04:29:51Z-
dc.date.available2018-12-14T04:29:51Z-
dc.date.issued2018-06-11-
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/2433/235708-
dc.description.abstractUterine leiomyoma is the most common benign tumour in women, and an appropriate animal model for leiomyoma would be useful for exploring new therapeutic strategies. Therefore, we have been challenged to develop a new simple mouse model for human leiomyoma. Leiomyoma tissues were harvested from myomas resected by different surgical procedures with or without gonadotropin-releasing hormone agonist (GnRHa) treatment and were subcutaneously implanted into BALB/c nude mice with an estradiol/progesterone-releasing pellet. The implanted leiomyoma tissues that were obtained from the marginal site of large myomas resected by abdominal myomectomy with GnRHa treatment exhibited sufficient tumour growth in the transplanted mice. The leiomyomas that were treated with GnRHa highly expressed the estrogen/progesterone receptor genes, insulin-like growth factor 2 (IGF2) and embryonic smooth muscle myosin heavy chain (SMemb), which suggests that these factors are critical in the establishment of a mouse model of growing leiomyoma. As a result, this model will be useful for the development of new therapeutic strategies.en
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherSpringer Natureen
dc.rights© The Author(s) 2018. 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.en
dc.titleEstablishment of a novel mouse xenograft model of human uterine leiomyomaen
dc.typejournal article-
dc.type.niitypeJournal Article-
dc.identifier.jtitleScientific Reportsen
dc.identifier.volume8-
dc.relation.doi10.1038/s41598-018-27138-1-
dc.textversionpublisher-
dc.identifier.artnum8872-
dc.addressDepartment of Obstetrics and Gynecology, Faculty of Medicine, Osaka Medical Collegeen
dc.addressDivision of Research Animal Laboratory and Translational Medicine, Research and Development Center, Osaka Medical College・Department of Pharmacology, Faculty of Medicine, Osaka Medical Collegeen
dc.addressDepartment of Legal Medicine, Faculty of Medicine, Osaka Medical Collegeen
dc.addressDepartment of Obstetrics and Gynecology, Faculty of Medicine, Osaka Medical Collegeen
dc.addressLaboratory of Biomaterials, Department of Regeneration Science and Engineering, Institute for Frontier Life and Medical Sciences, Kyoto Universityen
dc.addressDepartment of Obstetrics and Gynecology, Faculty of Medicine, Osaka Medical Collegeen
dc.addressDepartment of Pharmacology, Faculty of Medicine, Osaka Medical Collegeen
dc.identifier.pmid29891843-
dcterms.accessRightsopen access-
出現コレクション:学術雑誌掲載論文等

アイテムの簡略レコードを表示する

Export to RefWorks


出力フォーマット 


このリポジトリに保管されているアイテムはすべて著作権により保護されています。