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Establishment of a novel mouse xenograft model of human uterine leiomyoma

机译:人子宫平滑肌瘤新型小鼠异种移植模型的建立

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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.
机译:子宫平滑肌瘤是女性中最常见的良性肿瘤,适合的平滑肌瘤动物模型对于探索新的治疗策略将很有用。因此,我们面临着开发人类平滑肌瘤新的简单小鼠模型的挑战。从通过不同手术方法切除的肌瘤中收集平滑肌瘤组织,并进行或不进行促性腺激素释放激素激动剂(GnRHa)处理,然后将其皮下植入雌二醇/孕激素释放颗粒的BALB / c裸鼠中。从经GnRHa治疗的腹部肌瘤切除术切除的大肌瘤边缘部位获得的植入的平滑肌瘤组织在移植小鼠中表现出足够的肿瘤生长。用GnRHa治疗的平滑肌瘤高表达雌激素/孕激素受体基因,胰岛素样生长因子2(IGF2)和胚胎平滑肌肌球蛋白重链(SMemb),这表明这些因子对建立小鼠模型至关重要平滑肌瘤的发展。结果,该模型将对开发新的治疗策略有用。

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