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Proteomic advance of ischemic stroke: preclinical, clinical, and intervention

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Metabolic Brain Disease Aims and scope Submit manuscript

Abstract

Ischemic stroke (IS) is the most common type of stroke and is characterized by high rates of mortality and long-term injury. The prediction and early diagnosis of IS are therefore crucial for optimal clinical intervention. Proteomics has provided important techniques for exploring protein markers associated with IS, but there has been no systematic evaluation and review of research that has used these techniques. Here, we review the differential proteins that have been found in cell- and animal- based studies and clinical trials of IS in the past 10 years; determine the key pathological proteins that have been identified in clinical trials; summarize the target proteins affected by interventions aimed at treating IS, with a focus on traditional Chinese medicine treatments. Overall, we clarify findings and problems that have been identified in recent proteomics research on IS and provide suggestions for improvements in this area. We also suggest areas that could be explored for determining the pathogenesis and developing interventions for IS.

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Data availability

The datasets supporting the conclusions of this article are available from the corresponding author.

Abbreviations

BBB:

Blood brain barrier

CSF:

Cerebrospinal fluid

DDA:

Data dependent analysis

DIA:

Data independent analysis

DIGE:

Differential gel electrophoresis

ELISA:

Enzyme-linked immunosorbent assay

ELVO:

Emergent large vessel occlusion

GO:

Gene Ontology

IPSCs:

Induced pluripotent stem cells

IS:

Ischemic stroke

I-R:

Ischemia-reperfusion

iTRAQ:

Isobaric tag for relative and absolute quantitation

KEGG:

Kyoto Encyclopedia of Genes and Genomes

LC:

Liquid chromatograph

MCAO:

Middle cerebral artery occlusion

MRM:

Multiple reaction monitoring

MS:

Mass spectrometry

MSCs:

Mesenchymal stem cells

PEA:

Proximity extension assay

PPI:

Protein-protein interaction

PRM:

Parallel reaction monitoring

PTM:

Post-translational modification

qPCR:

Real-time quantitative polymerase chain reaction

SRM:

Selected reaction monitoring

TCM:

Traditional Chinese medicine

TMT:

Tandem mass tag

t-PA:

Tissue plasminogen activator

WB:

Western blot

2DE/2D-PAGE:

Two-dimensional gel electrophoresis

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Acknowledgements

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Funding

The study was supported by grants from by National Natural Science Foundation of China (82173648), the Medical and Health Science and Technology Project in Zhejiang province (2023KY1136), Ningbo Hwa Mei Research Fund (2022HMZY101, 2023HMZD01 and 2021HMKY14).

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Contributions

Tian Zhao, Yuyi Sha and Liyuan Han contributed to the study conception and design. Tian Zhao wrote first draft of the manuscript. Tian Zhao and Liyuan Han revised and edited the manuscript. All authors commented on previous versions of the manuscript and all authors read and approved the final manuscript.

Corresponding authors

Correspondence to Yuyi Sha or Liyuan Han.

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The authors have no relevant financial or non-financial interests to disclose.

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Zhao, T., Zeng, J., Zhang, R. et al. Proteomic advance of ischemic stroke: preclinical, clinical, and intervention. Metab Brain Dis 38, 2521–2546 (2023). https://doi.org/10.1007/s11011-023-01262-y

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  • DOI: https://doi.org/10.1007/s11011-023-01262-y

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