• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

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.

DOI:10.1095/biolreprod64.4.1122
PMID:11259258
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。

相似文献

1
Ovarian tumorigenesis in mice transgenic for murine inhibin alpha subunit promoter-driven Simian Virus 40 T-antigen: ontogeny, functional characteristics, and endocrine effects.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
Biol Reprod. 2001 Apr;64(4):1122-30. doi: 10.1095/biolreprod64.4.1122.
2
High levels of luteinizing hormone analog stimulate gonadal and adrenal tumorigenesis in mice transgenic for the mouse inhibin-alpha-subunit promoter/Simian virus 40 T-antigen fusion gene.高水平的促黄体生成素类似物可刺激携带小鼠抑制素α亚基启动子/猿猴病毒40 T抗原融合基因的转基因小鼠发生性腺和肾上腺肿瘤。
Oncogene. 2003 May 22;22(21):3269-78. doi: 10.1038/sj.onc.1206518.
3
Direct luteinizing hormone action triggers adrenocortical tumorigenesis in castrated mice transgenic for the murine inhibin alpha-subunit promoter/simian virus 40 T-antigen fusion gene.直接促黄体生成素作用引发了在因小鼠抑制素α亚基启动子/猿猴病毒40 T抗原融合基因而转基因的去势小鼠中的肾上腺皮质肿瘤发生。
Mol Endocrinol. 1998 Jun;12(6):801-9. doi: 10.1210/mend.12.6.0117.
4
Transgenic mice expressing inhibin α-subunit promoter (inhα)/Simian Virus 40 T-antigen (Tag) transgene as a model for the therapy of granulosa cell-derived ovarian cancer.表达抑制素 α 亚单位启动子 (inhα)/猿猴病毒 40 T 抗原 (Tag) 转基因的转基因小鼠作为治疗颗粒细胞来源的卵巢癌的模型。
Reprod Biol. 2014 Mar;14(1):25-31. doi: 10.1016/j.repbio.2013.11.005. Epub 2013 Dec 11.
5
Gonadal tumorigenesis in transgenic mice bearing the mouse inhibin alpha-subunit promoter/simian virus T-antigen fusion gene: characterization of ovarian tumors and establishment of gonadotropin-responsive granulosa cell lines.携带小鼠抑制素α亚基启动子/猿猴病毒T抗原融合基因的转基因小鼠的性腺肿瘤发生:卵巢肿瘤的特征及促性腺激素反应性颗粒细胞系的建立。
Mol Endocrinol. 1995 May;9(5):616-27. doi: 10.1210/mend.9.5.7565808.
6
Suppression of gonadotropins inhibits gonadal tumorigenesis in mice transgenic for the mouse inhibin alpha-subunit promoter/simian virus 40 T-antigen fusion gene.促性腺激素的抑制可抑制转小鼠抑制素α亚基启动子/猴病毒40 T抗原融合基因的转基因小鼠的性腺肿瘤发生。
Endocrinology. 1997 Aug;138(8):3521-31. doi: 10.1210/endo.138.8.5316.
7
Gonadal tumors of mice double transgenic for inhibin-alpha promoter-driven simian virus 40 T-antigen and herpes simplex virus thymidine kinase are sensitive to ganciclovir treatment.对于同时转染抑制素α启动子驱动的猿猴病毒40 T抗原和单纯疱疹病毒胸苷激酶的双转基因小鼠,其性腺肿瘤对更昔洛韦治疗敏感。
J Endocrinol. 2001 Jul;170(1):79-90. doi: 10.1677/joe.0.1700079.
8
Cyclin D2 and p27 are tissue-specific regulators of tumorigenesis in inhibin alpha knockout mice.细胞周期蛋白D2和p27是抑制素α基因敲除小鼠肿瘤发生的组织特异性调节因子。
Mol Endocrinol. 2003 Oct;17(10):2053-69. doi: 10.1210/me.2003-0038. Epub 2003 Jul 10.
9
Gonadectomy permits adrenocortical tumorigenesis in mice transgenic for the mouse inhibin alpha-subunit promoter/simian virus 40 T-antigen fusion gene: evidence for negative autoregulation of the inhibin alpha-subunit gene.性腺切除术可使转小鼠抑制素α亚基启动子/猴病毒40 T抗原融合基因的小鼠发生肾上腺皮质肿瘤:抑制素α亚基基因负向自调控的证据。
Mol Endocrinol. 1996 Dec;10(12):1667-77. doi: 10.1210/mend.10.12.8961275.
10
Adrenocortical tumorigenesis in transgenic mice: the role of luteinizing hormone receptor and transcription factors GATA-4 and GATA-61.转基因小鼠中的肾上腺皮质肿瘤发生:促黄体生成素受体以及转录因子GATA-4和GATA-6的作用1。
Reprod Biol. 2001 Jul;1(1):5-9.

引用本文的文献

1
Molecular mechanisms underlying mifepristone's agonistic action on ovarian cancer progression.米非司酮促进卵巢癌进展的作用机制。
EBioMedicine. 2019 Sep;47:170-183. doi: 10.1016/j.ebiom.2019.08.035. Epub 2019 Aug 26.
2
Toying with fate: Redirecting the differentiation of adrenocortical progenitor cells into gonadal-like tissue.玩弄命运:将肾上腺皮质祖细胞的分化重定向为性腺样组织。
Mol Cell Endocrinol. 2015 Jun 15;408:165-77. doi: 10.1016/j.mce.2014.12.003. Epub 2014 Dec 8.
3
Development of a syngeneic mouse model of epithelial ovarian cancer.
建立上皮性卵巢癌同源小鼠模型。
J Ovarian Res. 2010 Oct 19;3:24. doi: 10.1186/1757-2215-3-24.
4
Xenograft and Transgenic Mouse Models of Epithelial Ovarian Cancer and Non Invasive Imaging Modalities to Monitor Ovarian Tumor Growth In situ -Applications in Evaluating Novel Therapeutic Agents.上皮性卵巢癌的异种移植和转基因小鼠模型以及监测原位卵巢肿瘤生长的非侵入性成像方式——在评估新型治疗药物中的应用
Curr Protoc Pharmacol. 2009 Jun 1;45:14.12.1-14.12.26.
5
A novel targeted therapy of Leydig and granulosa cell tumors through the luteinizing hormone receptor using a hecate-chorionic gonadotropin beta conjugate in transgenic mice.在转基因小鼠中,通过使用赫卡忒 - 绒毛膜促性腺激素β缀合物,经由促黄体生成素受体对睾丸间质细胞瘤和颗粒细胞瘤进行新型靶向治疗。
Neoplasia. 2005 May;7(5):497-508. doi: 10.1593/neo.04751.