全面的蛋白质组分析揭示了组织学亚型中早期妊娠丢失的不同特征和诊断生物标记物面板。

IF 6.1 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Yating Zhao, Yingjiqiong Liang, Luya Cai, Limeng Cai, Bo Huang, Peilin Han, Xiaofei Zhang, Huifang Zhang, Zhen Chen, Xiangang Yin, Ping Duan, Huafeng Shou, Xiaoxu Zhu, Zhe Wang, Qihong Wan, Jinyan Huang, Jianhua Qian
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引用次数: 0

摘要

早孕流产(EPL)是人类生殖过程中的常见现象,可分为组织学亚型,如水样流产(HA)和水滴形痣(HMs),包括完全水滴形痣(CHMs)和部分水滴形痣(PHMs)。然而,由于误诊率高和不同的预后风险,准确诊断和改善患者管理仍具有挑战性。因此,急需针对 EPL 的诊断生物标志物。我们的研究旨在通过全面的蛋白质组分析确定 EPL 的生物标志物。研究使用了10个CHMs、6个PHMs、10个HAs和10个正常对照(NC)受孕产物(POC),以获得蛋白质组画像。平行反应监测(PRM)靶向蛋白质组分析和回归分析用于验证和筛选诊断特征。最后,选出了 14 个蛋白质,并建立了一个诊断分类器面板(DLK1、SPTB/COL21A1 和 SAR1A)来代表 CHM、PHM 和 NC 组(auROC 分别为 0.900、0.804/0.885 和 0.991)。通过免疫组化(IHC)(120 人)和免疫印迹(WB)分析(28 人),这一高诊断能力在另一个独立队列(148 人)中得到了进一步验证。蛋白质 SPTB 被选中用于进一步的体外生物学行为实验。我们的数据表明,SPTB 可维持滋养层细胞的增殖、血管生成、细胞运动和细胞骨架网络。这项研究提供了一个全面的蛋白质组图谱,并确定了潜在的诊断生物标志物。这些发现加深了我们对 EPL 发病机制的了解,并为诊断和治疗干预提供了新的靶点。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comprehensive Proteomic Analysis Reveals Distinct Features and a Diagnostic Biomarker Panel for Early Pregnancy Loss in Histological Subtypes.

Early pregnancy loss (EPL) is a common event in human reproduction and is classified into histological subtypes such as hydropic abortion (HA) and hydatidiform moles, including complete hydatidiform moles (CHMs) and partial hydatidiform moles (PHMs). However, accurate diagnosis and improved patient management remain challenging due to high rates of misdiagnosis and diverse prognostic risks. Therefore, diagnostic biomarkers for EPL are urgently needed. Our study aimed to identify biomarkers for EPL through comprehensive proteomic analysis. Ten CHMs, six PHMs, ten HAs, and 10 normal control products of conception were used to obtain a proteomic portrait. Parallel reaction monitoring-targeted proteomic and regression analyses were used to verify and select the diagnostic signatures. Finally, 14 proteins were selected and a panel of diagnostic classifiers (DLK1, SPTB/COL21A1, and SAR1A) was built to represent the CHM, PHM, and normal control groups (area under the receiver operating characteristic curve = 0.900, 0.804/0.885, and 0.991, respectively). This high diagnostic power was further validated in another independent cohort (n = 148) by immunohistochemistry (n = 120) and Western blot analyses (n = 28). The protein SPTB was selected for further biological behavior experiments in vitro. Our data suggest that SPTB maintains trophoblast cell proliferation, angiogenesis, cell motility, and the cytoskeleton network. This study provides a comprehensive proteomic portrait and identifies potential diagnostic biomarkers. These findings enhance our understanding of EPL pathogenesis and offer novel targets for diagnosis and therapeutic interventions.

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来源期刊
Molecular & Cellular Proteomics
Molecular & Cellular Proteomics 生物-生化研究方法
CiteScore
11.50
自引率
4.30%
发文量
131
审稿时长
84 days
期刊介绍: The mission of MCP is to foster the development and applications of proteomics in both basic and translational research. MCP will publish manuscripts that report significant new biological or clinical discoveries underpinned by proteomic observations across all kingdoms of life. Manuscripts must define the biological roles played by the proteins investigated or their mechanisms of action. The journal also emphasizes articles that describe innovative new computational methods and technological advancements that will enable future discoveries. Manuscripts describing such approaches do not have to include a solution to a biological problem, but must demonstrate that the technology works as described, is reproducible and is appropriate to uncover yet unknown protein/proteome function or properties using relevant model systems or publicly available data. Scope: -Fundamental studies in biology, including integrative "omics" studies, that provide mechanistic insights -Novel experimental and computational technologies -Proteogenomic data integration and analysis that enable greater understanding of physiology and disease processes -Pathway and network analyses of signaling that focus on the roles of post-translational modifications -Studies of proteome dynamics and quality controls, and their roles in disease -Studies of evolutionary processes effecting proteome dynamics, quality and regulation -Chemical proteomics, including mechanisms of drug action -Proteomics of the immune system and antigen presentation/recognition -Microbiome proteomics, host-microbe and host-pathogen interactions, and their roles in health and disease -Clinical and translational studies of human diseases -Metabolomics to understand functional connections between genes, proteins and phenotypes
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