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肝纤维化中的高尔基蛋白 73。

Golgi protein 73 in liver fibrosis.

机构信息

Department of Laboratory Medicine, Nicolaus Copernicus University in Torun, Collegium Medicum in Bydgoszcz, Poland.

Department of Laboratory Medicine, Nicolaus Copernicus University in Torun, Collegium Medicum in Bydgoszcz, Poland.

出版信息

Clin Chim Acta. 2025 Jan 15;565:119999. doi: 10.1016/j.cca.2024.119999. Epub 2024 Oct 12.

Abstract

Golgi protein 73 (GP73) is implicated in key pathogenic processes, particularly those related to inflammation and fibrogenesis. In the last years, its measurement has emerged as a promising biomarker for detection of liver fibrosis (LF), a common consequence of chronic liver disease that can progress to cirrhosis and eventually hepatocellular carcinoma. GP73 concentrations in blood appear significantly increased in LF patients, correlating with disease severity, making this biomarker a possible non-invasive alternative for detecting and monitoring this condition regardless of etiology. Understanding the molecular mechanisms involving GP73 expression could also lead to new therapeutic strategies aimed at modulating its synthesis or function to prevent or reverse LF. Despite its clinical potential, GP73 as a LF biomarker faces several challenges. The lack of demonstrated comparability among different assays as well as the lack of knowledge of individual variability can make difficult the result interpretation. Further research is therefore needed focusing on robust clinical validation of GP73 as a LF biomarker. Addressing analytical, biological, and clinical limitations will be critical to exploiting its potential for improving detection and monitoring of advanced LF.

摘要

高尔基蛋白 73(GP73)与关键的致病过程有关,特别是与炎症和纤维化有关。在过去的几年中,其测量已经成为检测肝纤维化(LF)的有前途的生物标志物,LF 是慢性肝病的常见后果,可进展为肝硬化,最终发展为肝细胞癌。LF 患者血液中的 GP73 浓度明显升高,与疾病严重程度相关,这使得该生物标志物成为一种可能的非侵入性替代方法,可用于检测和监测无论病因如何的这种疾病。了解涉及 GP73 表达的分子机制也可能导致新的治疗策略,旨在调节其合成或功能以预防或逆转 LF。尽管具有临床潜力,但 GP73 作为 LF 生物标志物仍面临几个挑战。缺乏不同检测方法之间的可比性证明,以及对个体差异的认识不足,使得结果解释变得困难。因此,需要进一步研究,重点是对 GP73 作为 LF 生物标志物进行稳健的临床验证。解决分析、生物学和临床方面的局限性对于挖掘其在提高晚期 LF 检测和监测方面的潜力至关重要。

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