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热休克蛋白在胎盘缺血性疾病中的作用:当前文献的叙述性综述

The role of heat shock proteins in placental ischemic disease: A narrative review of the current literature.

作者信息

Samara Athina A, Lafioniatis Anastasios, Ioannou Maria, Tsiapakidou Sofia, Gerede Angeliki, Anastasakis Eleftherios, Daponte Alexandros, Sotiriou Sotirios

机构信息

Department of Embryology, Faculty of Medicine, University of Thessaly, Larissa, Greece.

Department of Obstetrics and Gynecology, University Hospital of Larissa, Larissa, Greece.

出版信息

Int J Gynaecol Obstet. 2025 Jun;169(3):960-967. doi: 10.1002/ijgo.70039. Epub 2025 Mar 3.

Abstract

Pre-eclampsia, placental abruption, and fetal growth restriction (FGR) are collectively referred to as placental ischemic disease (PID). Heat shock proteins (HSPs), originally considered as a response to the heat shock, have a central role in regulating the cellular functions by quality controlling the newly synthesized proteins. The aim of the present review is to investigate the expression of the HSPs in PID and their potential role as biomarkers, based on the available data in the literature. A considerable amount of research has been conducted in order to determine the significance of HSPs in placental pathology and insufficiency, using both immunochemistry and circulating mRNA approaches. HSPs seem to be promising biomarkers that could be used for screening and monitoring the cellular stress of the placenta and its dysfunction. Yet, in order to be able to reach more solid evidence and draw a safer conclusion regarding their utility in clinical practice there is still a long way to go and further well-designed greater scale studies are required.

摘要

子痫前期、胎盘早剥和胎儿生长受限(FGR)统称为胎盘缺血性疾病(PID)。热休克蛋白(HSPs)最初被认为是对热休克的一种反应,通过对新合成蛋白质进行质量控制在调节细胞功能中起核心作用。本综述的目的是根据文献中的现有数据,研究HSPs在PID中的表达及其作为生物标志物的潜在作用。为了确定HSPs在胎盘病理和功能不全中的意义,已经使用免疫化学和循环mRNA方法进行了大量研究。HSPs似乎是很有前景的生物标志物,可用于筛查和监测胎盘的细胞应激及其功能障碍。然而,为了能够获得更确凿的证据并就其在临床实践中的效用得出更可靠的结论,仍有很长的路要走,需要进一步开展设计更合理、规模更大的研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9731/12093934/331f8e71413f/IJGO-169-960-g001.jpg

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