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阿尔茨海默病患者尿液蛋白质组的分子网络分析

Molecular Network Analysis of the Urinary Proteome of Alzheimer's Disease Patients.

作者信息

Watanabe Yumi, Hirao Yoshitoshi, Kasuga Kensaku, Tokutake Takayoshi, Semizu Yuka, Kitamura Kaori, Ikeuchi Takeshi, Nakamura Kazutoshi, Yamamoto Tadashi

机构信息

Division of Preventive Medicine, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Biofluid Biomarker Center, Niigata University, Niigata, Japan.

出版信息

Dement Geriatr Cogn Dis Extra. 2019 Feb 8;9(1):53-65. doi: 10.1159/000496100. eCollection 2019 Jan-Apr.

Abstract

BACKGROUND/AIMS: The identification of predictive biomarkers for Alzheimer's disease (AD) from urine would aid in screening for the disease, but information about biological and pathophysiological changes in the urine of AD patients is limited. This study aimed to explore the comprehensive profile and molecular network relations of urinary proteins in AD patients.

METHODS

Urine samples collected from 18 AD patients and 18 age- and sex-matched cognitively normal controls were analyzed by mass spectrometry and semiquantified with the normalized spectral index method. Bioinformatics analyses were performed on proteins which significantly increased by more than 2-fold or decreased by less than 0.5-fold compared to the control ( < 0.05) using DAVID bioinformatics resources and KeyMolnet software.

RESULTS

The levels of 109 proteins significantly differed between AD patients and controls. Among these, annotation clusters related to lysosomes, complement activation, and gluconeogenesis were significantly enriched. The molecular relation networks derived from these proteins were mainly associated with pathways of lipoprotein metabolism, heat shock protein 90 signaling, matrix metalloproteinase signaling, and redox regulation by thioredoxin.

CONCLUSION

Our findings suggest that changes in the urinary proteome of AD patients reflect systemic changes related to AD pathophysiology.

摘要

背景/目的:从尿液中鉴定阿尔茨海默病(AD)的预测生物标志物将有助于该疾病的筛查,但关于AD患者尿液中生物学和病理生理学变化的信息有限。本研究旨在探索AD患者尿液蛋白质的综合概况和分子网络关系。

方法

收集18例AD患者和18例年龄及性别匹配的认知正常对照的尿液样本,采用质谱分析并用归一化光谱指数法进行半定量。使用DAVID生物信息学资源和KeyMolnet软件对与对照相比显著增加超过2倍或减少小于0.5倍(<0.05)的蛋白质进行生物信息学分析。

结果

AD患者和对照之间109种蛋白质的水平存在显著差异。其中,与溶酶体、补体激活和糖异生相关的注释簇显著富集。源自这些蛋白质的分子关系网络主要与脂蛋白代谢、热休克蛋白90信号传导、基质金属蛋白酶信号传导和硫氧还蛋白的氧化还原调节途径相关。

结论

我们的研究结果表明,AD患者尿液蛋白质组的变化反映了与AD病理生理学相关的全身变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f72a/6477484/780d5ef4ec25/dee-0009-0053-g01.jpg

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