Establishment of a novel mouse xenograft model of human uterine leiomyoma

被引:9
作者
Suzuki, Yusuke [1 ]
Ii, Masaaki [2 ,3 ]
Saito, Takashi [4 ]
Terai, Yoshito [1 ]
Tabata, Yasuhiko [5 ]
Ohmichi, Masahide [1 ]
Asahi, Michio [3 ]
机构
[1] Osaka Med Coll, Dept Obstet & Gynecol, Fac Med, Osaka, Japan
[2] Osaka Med Coll, Div Res Anim Lab & Translat Med, Res & Dev Ctr, Osaka, Japan
[3] Osaka Med Coll, Dept Pharmacol, Fac Med, Osaka, Japan
[4] Osaka Med Coll, Dept Legal Med, Fac Med, Osaka, Japan
[5] Kyoto Univ, Lab Biomat, Dept Regenerat Sci & Engn, Inst Frontier Life & Med Sci, Kyoto, Japan
基金
日本学术振兴会;
关键词
HUMAN MYOMETRIUM; EXPRESSION; FIBROIDS;
D O I
10.1038/s41598-018-27138-1
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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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页数:11
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