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循环嗜铬粒蛋白 A 及其片段作为诊断和预后疾病标志物。

Circulating chromogranin A and its fragments as diagnostic and prognostic disease markers.

机构信息

Division of Experimental Oncology, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Vita-Salute San Raffaele University, Milan, Italy.

出版信息

Pflugers Arch. 2018 Jan;470(1):199-210. doi: 10.1007/s00424-017-2030-y. Epub 2017 Oct 10.

Abstract

Chromogranin A (CgA), a secretory protein released in the blood by neuroendocrine cells and neurons, is the precursor of various bioactive fragments involved in the regulation of the cardiovascular system, metabolism, innate immunity, angiogenesis, and tissue repair. After the original demonstration that circulating CgA can serve as a biomarker for a wide range of neuroendocrine tumors, several studies have shown that increased levels of CgA can be present also in the blood of patients with cardiovascular, gastrointestinal, and inflammatory diseases with, in certain cases, important diagnostic and prognostic implications. Considering the high structural and functional heterogeneity of the CgA system, comprising precursor and fragments, it is not surprising that the different immunoassays used in these studies led, in some cases, to discrepant results. Here, we review these notions and we discuss the importance of measuring total-CgA, full-length CgA, specific fragments, and their relative levels for a more thorough assessment of the pathophysiological function and diagnostic/prognostic value of the CgA system.

摘要

嗜铬粒蛋白 A(CgA)是一种由神经内分泌细胞和神经元在血液中释放的分泌蛋白,是参与心血管系统、代谢、先天免疫、血管生成和组织修复调节的各种生物活性片段的前体。最初的研究表明,循环 CgA 可以作为广泛的神经内分泌肿瘤的生物标志物,此后的多项研究表明,心血管疾病、胃肠道疾病和炎症性疾病患者的血液中也可能存在 CgA 水平升高,在某些情况下,这具有重要的诊断和预后意义。鉴于 CgA 系统(包括前体和片段)具有高度的结构和功能异质性,因此,在这些研究中使用的不同免疫测定方法在某些情况下导致了不一致的结果,这并不奇怪。在这里,我们回顾了这些概念,并讨论了测量总 CgA、全长 CgA、特异性片段及其相对水平的重要性,以便更全面地评估 CgA 系统的病理生理功能和诊断/预后价值。

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