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Establishment of a novel mouse xenograft model of human uterine leiomyoma
Uterine 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 myoma...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995841/ https://www.ncbi.nlm.nih.gov/pubmed/29891843 http://dx.doi.org/10.1038/s41598-018-27138-1 |
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author | Suzuki, Yusuke Ii, Masaaki Saito, Takashi Terai, Yoshito Tabata, Yasuhiko Ohmichi, Masahide Asahi, Michio |
author_facet | Suzuki, Yusuke Ii, Masaaki Saito, Takashi Terai, Yoshito Tabata, Yasuhiko Ohmichi, Masahide Asahi, Michio |
author_sort | Suzuki, Yusuke |
collection | PubMed |
description | Uterine 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. |
format | Online Article Text |
id | pubmed-5995841 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-59958412018-06-21 Establishment of a novel mouse xenograft model of human uterine leiomyoma Suzuki, Yusuke Ii, Masaaki Saito, Takashi Terai, Yoshito Tabata, Yasuhiko Ohmichi, Masahide Asahi, Michio Sci Rep Article Uterine 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. Nature Publishing Group UK 2018-06-11 /pmc/articles/PMC5995841/ /pubmed/29891843 http://dx.doi.org/10.1038/s41598-018-27138-1 Text en © The Author(s) 2018 Open Access 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/. |
spellingShingle | Article Suzuki, Yusuke Ii, Masaaki Saito, Takashi Terai, Yoshito Tabata, Yasuhiko Ohmichi, Masahide Asahi, Michio Establishment of a novel mouse xenograft model of human uterine leiomyoma |
title | Establishment of a novel mouse xenograft model of human uterine leiomyoma |
title_full | Establishment of a novel mouse xenograft model of human uterine leiomyoma |
title_fullStr | Establishment of a novel mouse xenograft model of human uterine leiomyoma |
title_full_unstemmed | Establishment of a novel mouse xenograft model of human uterine leiomyoma |
title_short | Establishment of a novel mouse xenograft model of human uterine leiomyoma |
title_sort | establishment of a novel mouse xenograft model of human uterine leiomyoma |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995841/ https://www.ncbi.nlm.nih.gov/pubmed/29891843 http://dx.doi.org/10.1038/s41598-018-27138-1 |
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