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小鼠中由鼠抑制素α亚基启动子驱动的猿猴病毒40 T抗原转基因导致的卵巢肿瘤发生:个体发生、功能特征及内分泌效应

Ovarian tumorigenesis in mice transgenic for murine inhibin alpha subunit promoter-driven Simian Virus 40 T-antigen: ontogeny, functional characteristics, and endocrine effects.

作者信息

Rahman N A, Huhtaniemi I T

机构信息

Department of Physiology, University of Turku, 20520 Turku, Finland.

出版信息

Biol Reprod. 2001 Apr;64(4):1122-30. doi: 10.1095/biolreprod64.4.1122.

Abstract

We previously reported formation of ovarian granulosa cell tumors with 100% penetration in a transgenic mouse model with murine inhibin alpha subunit promoter-driven (inhalpha)/Simian Virus 40 T-antigen (Tag). The tumor-bearing inhalpha/Tag mice showed highly elevated serum levels of immunoreactive inhibin. To investigate the onset of tumorigenesis and related endocrine consequences, 6-8 female mice of two inhalpha/Tag lines and their mating control littermates were killed monthly between 1 and 6 mo of age. We also investigated tumorigenesis-related fertility aspects of these two mouse lines. The ontogeny and progression of tumors could be monitored in both inhalpha/Tag lines by alterations of ovarian weights and serum hormone levels. Serum progesterone levels increased in both inhalpha/Tag lines in an age-dependent manner as ovarian tumorigenesis progressed, and a reciprocal decrease occurred in serum LH and FSH. Neither serum estradiol (E(2)) nor uterine weights were significantly altered during tumorigenesis, suggesting that the ovarian tumors represented late stages of granulosa cell differentiation. In conclusion, the present findings show in the inhalpha/Tag TG mice a relation between endocrine consequences of granulosa cell tumorigenesis, and a connection of onset of tumor formation with aberrant steroidogenesis and gonadotropin secretion. These findings indicate that tumors are endocrinologically active and able to exert enhanced negative feedback effects on pituitary function. The tumors provide a good model for endocrinologically active hormone-dependent tumors.

摘要

我们先前报道,在一种由鼠抑制素α亚基启动子驱动(inhalpha)/猿猴病毒40 T抗原(Tag)的转基因小鼠模型中,卵巢颗粒细胞瘤的形成率达100%。携带肿瘤的inhalpha/Tag小鼠血清中免疫反应性抑制素水平显著升高。为了研究肿瘤发生的起始及相关内分泌后果,在1至6月龄期间,每月处死6 - 8只两个inhalpha/Tag品系的雌性小鼠及其作为交配对照的同窝仔鼠。我们还研究了这两个小鼠品系与肿瘤发生相关的生育方面。通过卵巢重量和血清激素水平的变化,可以监测两个inhalpha/Tag品系中肿瘤的发生和发展。随着卵巢肿瘤发生的进展,两个inhalpha/Tag品系的血清孕酮水平均呈年龄依赖性增加,而血清促黄体生成素(LH)和促卵泡生成素(FSH)则呈相反下降。在肿瘤发生过程中,血清雌二醇(E₂)和子宫重量均无显著变化,这表明卵巢肿瘤代表了颗粒细胞分化的晚期阶段。总之,目前的研究结果表明,在inhalpha/Tag转基因小鼠中,颗粒细胞瘤发生的内分泌后果之间存在关联,肿瘤形成的起始与异常的类固醇生成和促性腺激素分泌有关。这些发现表明肿瘤具有内分泌活性,能够对垂体功能产生增强的负反馈作用。这些肿瘤为具有内分泌活性的激素依赖性肿瘤提供了一个良好的模型。

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