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疾病机制:垂体肿瘤的发病机制。

Mechanisms of disease: The pathogenesis of pituitary tumors.

作者信息

Ezzat Shereen, Asa Sylvia L

机构信息

The Freeman Centre for Endocrine Oncology, Mount Sinai Hospital, Toronto, Ontario, Canada.

出版信息

Nat Clin Pract Endocrinol Metab. 2006 Apr;2(4):220-30. doi: 10.1038/ncpendmet0159.

DOI:10.1038/ncpendmet0159
PMID:16932287
Abstract

Pituitary tumors exhibit a spectrum of biology, with variable growth and hormonal behaviors. They therefore provide an opportunity to examine pathogenetic mechanisms that underlie the neoplastic process. These include alterations in hormone regulation, growth-factor stimulation, cell-cycle control and cell-stromal interactions that result from genetic mutations or epigenetic disruption of gene expression. Mouse models have validated the roles of these alterations, which can be targets for the development of therapies that can manage these lesions. These therapies are increasingly recognized as critical for quality of life.

摘要

垂体肿瘤表现出一系列生物学特性,其生长和激素行为各不相同。因此,它们为研究肿瘤形成过程背后的致病机制提供了一个机会。这些机制包括激素调节、生长因子刺激、细胞周期控制以及细胞与基质相互作用的改变,这些改变是由基因突变或基因表达的表观遗传破坏引起的。小鼠模型已经证实了这些改变的作用,它们可以成为开发治疗这些病变的疗法的靶点。这些疗法对于生活质量的重要性日益得到认可。

相似文献

1
Mechanisms of disease: The pathogenesis of pituitary tumors.疾病机制:垂体肿瘤的发病机制。
Nat Clin Pract Endocrinol Metab. 2006 Apr;2(4):220-30. doi: 10.1038/ncpendmet0159.
2
Transgenic and knockout mouse models clarify pituitary development, function and disease.转基因和基因敲除小鼠模型阐明了垂体的发育、功能及疾病。
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3
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2004 World Health Organization classification of pituitary tumors: what is new?2004年世界卫生组织垂体肿瘤分类:有哪些新内容?
Acta Neuropathol. 2006 Jan;111(1):78-9. doi: 10.1007/s00401-005-1102-9. Epub 2005 Nov 23.
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Molecular genetics of the cAMP-dependent protein kinase pathway and of sporadic pituitary tumorigenesis.环磷酸腺苷(cAMP)依赖性蛋白激酶途径与散发性垂体瘤发生的分子遗传学
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The pathogenesis of pituitary tumours.垂体肿瘤的发病机制。
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[Classification and pathophysiology of pituitary adenomas].[垂体腺瘤的分类与病理生理学]
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Pituitary tumors and hyperplasia in multiple endocrine neoplasia type 1 syndrome (MEN1): a case-control study in a series of 77 patients versus 2509 non-MEN1 patients.多发性内分泌腺瘤1型综合征(MEN1)中的垂体肿瘤和增生:一项针对77例患者与2509例非MEN1患者的病例对照研究。
Am J Surg Pathol. 2008 Apr;32(4):534-43. doi: 10.1097/PAS.0b013e31815ade45.

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PER2 integrates circadian disruption and pituitary tumorigenesis.PER2 将扰乱生物钟和引发垂体肿瘤结合在一起。
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Endocr Pathol. 2021 Mar;32(1):3-16. doi: 10.1007/s12022-021-09663-4. Epub 2021 Jan 12.
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MSH6/2 and PD-L1 Expressions Are Associated with Tumor Growth and Invasiveness in Silent Pituitary Adenoma Subtypes.MSH6/2 和 PD-L1 的表达与静默型垂体腺瘤亚型的肿瘤生长和侵袭性相关。
Int J Mol Sci. 2020 Apr 18;21(8):2831. doi: 10.3390/ijms21082831.
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MicroRNA-143 shows tumor suppressive effects through inhibition of oncogenic K-Ras in pituitary tumor.微小RNA-143通过抑制垂体肿瘤中的致癌性K-Ras发挥肿瘤抑制作用。
Int J Clin Exp Pathol. 2017 Nov 1;10(11):10969-10978. eCollection 2017.
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Hormonal aggressiveness according to the expression of cellular markers in corticotroph adenomas.根据促肾上腺皮质激素腺瘤细胞标志物的表达判断其激素侵袭性。
Endocrine. 2019 Apr;64(1):147-156. doi: 10.1007/s12020-018-1815-x. Epub 2018 Nov 24.
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The Molecular Pathology of Cushing Disease: Are We Nearly There?库欣病的分子病理学:我们快成功了吗?
J Endocr Soc. 2017 Feb 1;1(2):144-148. doi: 10.1210/js.2017-00036.
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MicroRNA-145 inhibits the activation of the mTOR signaling pathway to suppress the proliferation and invasion of invasive pituitary adenoma cells by targeting AKT3 in vivo and in vitro.微小RNA-145在体内和体外通过靶向AKT3抑制mTOR信号通路的激活,从而抑制侵袭性垂体腺瘤细胞的增殖和侵袭。
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