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Minerva Endocrinol (Torino). 2025 Jun;50(2):182-193. doi: 10.23736/S2724-6507.24.04270-2. Epub 2025 Feb 25.
2
Zebrafish model in the relentless race to tyrosine kinase inhibitors for neuroendocrine neoplasms.
Minerva Endocrinol (Torino). 2024 Dec;49(4):353-355. doi: 10.23736/S2724-6507.24.04308-2. Epub 2024 Nov 20.
3
Adrenal Disease in Small Mammals.小型哺乳动物的肾上腺疾病。
Vet Clin North Am Exot Anim Pract. 2025 Jan;28(1):87-106. doi: 10.1016/j.cvex.2024.07.003. Epub 2024 Oct 15.
4
Comparison of clinical, hormonal, pathological and treatment outcomes of ectopic Cushing's syndrome by sex: results of a multicenter study.比较不同性别异位库欣综合征的临床、激素、病理和治疗结果:一项多中心研究的结果。
Endocrine. 2024 Dec;86(3):1148-1155. doi: 10.1007/s12020-024-04004-x. Epub 2024 Sep 17.
5
How to manage Cushing's disease after failed primary pituitary surgery.原发性垂体手术后库欣病的治疗。
Eur J Endocrinol. 2024 Aug 30;191(3):R37-R54. doi: 10.1093/ejendo/lvae110.
6
High-throughput Screening for Cushing Disease: Therapeutic Potential of Thiostrepton via Cell Cycle Regulation.高通量筛选库欣病:硫链丝菌素通过细胞周期调控的治疗潜力。
Endocrinology. 2024 Jul 26;165(9). doi: 10.1210/endocr/bqae089.
7
Metformin inhibits cell proliferation and ACTH secretion in AtT20 cells via regulating the MAPK pathway.二甲双胍通过调节 MAPK 通路抑制 AtT20 细胞的增殖和 ACTH 分泌。
Mol Cell Endocrinol. 2024 Mar 1;582:112140. doi: 10.1016/j.mce.2023.112140. Epub 2023 Dec 24.
8
Circulating myomiRNAs as biomarkers in patients with Cushing's syndrome.循环肌微小 RNA 作为库欣综合征患者的生物标志物。
J Endocrinol Invest. 2024 Mar;47(3):655-669. doi: 10.1007/s40618-023-02184-3. Epub 2023 Sep 8.
9
Neuromedin B receptor as a potential therapeutic target for corticotroph adenomas.神经调节素 B 受体作为促肾上腺皮质腺瘤的潜在治疗靶点。
Pituitary. 2023 Oct;26(5):597-610. doi: 10.1007/s11102-023-01350-3. Epub 2023 Aug 29.
10
2023 AAHA Selected Endocrinopathies of Dogs and Cats Guidelines.2023年美国动物医院协会犬猫内分泌疾病精选指南
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动物王国中的库欣病:对人类医学的转化性见解

Cushing's Disease in the Animal Kingdom: Translational Insights for Human Medicine.

作者信息

Massardi Elena, Gaudenzi Germano, Carra Silvia, Oldani Monica, Rybinska Ilona, Persani Luca, Vitale Giovanni

机构信息

Department of Medical Biotechnology and Translational Medicine, University of Milan, 20129 Milan, Italy.

Laboratory of Geriatric and Oncologic Neuroendocrinology Research, IRCCS, Istituto Auxologico Italiano, Cusano Milanino, 20095 Milan, Italy.

出版信息

Int J Mol Sci. 2025 Sep 4;26(17):8626. doi: 10.3390/ijms26178626.

DOI:10.3390/ijms26178626
PMID:40943544
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12429187/
Abstract

Cushing's disease (CD) is a rare neuroendocrine disorder caused by ACTH-secreting pituitary adenomas, presenting significant diagnostic and therapeutic challenges. Given the evolutionary conservation of the hypothalamic-pituitary-adrenal axis, this review explores the translational value of spontaneous CD forms in dogs, horses, cats, small mammals, and rats, as well as of experimental models in mice, rats, and zebrafish. Dogs are the most studied, showing strong molecular and clinical similarities with human CD, making them valuable for preclinical drug and diagnostic research. While equine and feline CD are less characterized, they may provide insights into dopaminergic therapies and glucocorticoid resistance. Nevertheless, practical and ethical challenges limit the experimental use of companion animals. In preclinical research, mouse models are widely used to study hypercortisolism and test therapeutic agents via transgenic and xenograft strategies. Conversely, few studies are available on a zebrafish transgenic model for CD, displaying pituitary corticotroph expansion and partial resistance to glucocorticoid-negative feedback at the larval stage, while adults exhibit hypercortisolism resembling the human phenotype. Future transplantable systems in zebrafish may overcome several limitations observed in mice, supporting CD research. Collectively, these animal models, each offering unique advantages and limitations, provide a diverse toolkit for advancing CD research and improving human clinical outcomes.

摘要

库欣病(CD)是一种由分泌促肾上腺皮质激素(ACTH)的垂体腺瘤引起的罕见神经内分泌疾病,带来了重大的诊断和治疗挑战。鉴于下丘脑-垂体-肾上腺轴的进化保守性,本综述探讨了犬、马、猫、小型哺乳动物和大鼠中自发性CD形式以及小鼠、大鼠和斑马鱼实验模型的转化价值。犬是研究最多的,与人类CD表现出强烈的分子和临床相似性,使其在临床前药物和诊断研究中具有价值。虽然马和猫的CD特征较少,但它们可能为多巴胺能疗法和糖皮质激素抵抗提供见解。然而,实际和伦理挑战限制了伴侣动物的实验使用。在临床前研究中,小鼠模型被广泛用于研究皮质醇增多症并通过转基因和异种移植策略测试治疗药物。相反,关于斑马鱼CD转基因模型的研究很少,该模型在幼虫阶段显示垂体促肾上腺皮质细胞扩张和对糖皮质激素负反馈的部分抵抗,而成年斑马鱼表现出类似人类表型的皮质醇增多症。斑马鱼未来的可移植系统可能克服在小鼠中观察到的几个局限性,支持CD研究。总体而言,这些动物模型各有独特的优势和局限性,为推进CD研究和改善人类临床结果提供了一个多样化的工具包。