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肾上腺内分泌学的最新进展:过去 10 年的重大发现及未来十年的发展方向。

An update on adrenal endocrinology: significant discoveries in the last 10 years and where the field is heading in the next decade.

机构信息

Section on Endocrinology and Genetics & Inter-Institute Endocrinology Training Program, Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD), National Institutes of Health (NIH), NIH-Clinical Research Center, 10 Center Drive, Building 10, Room 1-3330, MSC1103, Bethesda, MD, 20892, USA.

出版信息

Hormones (Athens). 2018 Dec;17(4):479-490. doi: 10.1007/s42000-018-0072-y. Epub 2018 Nov 19.

Abstract

The last 10 years have produced an amazing number of significant discoveries in the field of adrenal endocrinology. The development of the adrenal gland was linked to specific molecules. Cortisol-producing lesions were associated mostly with defects of the cyclic AMP (cAMP) signaling pathway, whereas aldosterone-producing lesions were found to be the result of defects in aldosterone biosynthesis or the potassium channel KCNJ5 and related molecules. Macronodular adrenal hyperplasia was linked to ARMC5 defects and new genes were found to be involved in adrenocortical cancer (ACC). The succinate dehydrogenase (SDH) enzyme was proven to be the most important molecular pathway involved in pheochromocytomas, along with several other genes. Adrenomedullary tumors are now largely molecularly elucidated. Unfortunately, most of these important discoveries have yet to produce new therapeutic tools for our patients with adrenal diseases: ACC in its advanced stages remains largely an untreatable disorder and malignant pheochromocytomas are equally hard to treat. Thus, the challenge for the next 10 years is to translate the important discoveries of the previous decade into substantial advances in the treatment of adrenal disorders and tumors.

摘要

过去 10 年在肾上腺内分泌学领域产生了大量重要的发现。肾上腺的发育与特定分子有关。产生皮质醇的病变主要与环磷酸腺苷(cAMP)信号通路的缺陷有关,而产生醛固酮的病变被发现是醛固酮生物合成或钾通道 KCNJ5 和相关分子缺陷的结果。大结节性肾上腺增生与 ARMC5 缺陷有关,并且发现新的基因参与了肾上腺皮质癌(ACC)。琥珀酸脱氢酶(SDH)酶被证明是嗜铬细胞瘤中最重要的分子途径,还有其他几个基因。现在,大部分肾上腺髓质肿瘤的分子机制已经阐明。不幸的是,这些重要发现中的大多数尚未为我们患有肾上腺疾病的患者带来新的治疗手段:晚期 ACC 仍然是一种难以治疗的疾病,恶性嗜铬细胞瘤同样难以治疗。因此,未来 10 年的挑战是将前十年的重要发现转化为治疗肾上腺疾病和肿瘤的实质性进展。

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