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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...

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Autores principales: Suzuki, Yusuke, Ii, Masaaki, Saito, Takashi, Terai, Yoshito, Tabata, Yasuhiko, Ohmichi, Masahide, Asahi, Michio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
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.
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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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