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      Multi-omics of extracellular vesicles: An integrative representation of functional mediators and perspectives on lung disease study

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          Abstract

          Extracellular vesicles are secreted by almost all cell types. EVs include a broader component known as exosomes that participate in cell–cell and tissue–tissue communication via carrying diverse biological signals from one cell type or tissue to another. EVs play roles as communication messengers of the intercellular network to mediate different physiological activities or pathological changes. In particular, most EVs are natural carriers of functional cargo such as DNA, RNA, and proteins, and thus they are relevant to advancing personalized targeted therapies in clinical practice. For the application of EVs, novel bioinformatic models and methods based on high-throughput technologies and multi-omics data are required to provide a deeper understanding of their biological and biomedical characteristics. These include qualitative and quantitative representation for identifying cargo markers, local cellular communication inference for tracing the origin and production of EVs, and distant organ communication reconstruction for targeting the influential microenvironment and transferable activators. Thus, this perspective paper introduces EVs in the context of multi-omics and provides an integrative bioinformatic viewpoint of the state of current research on EVs and their applications.

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          Most cited references55

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          Glypican-1 identifies cancer exosomes and detects early pancreatic cancer.

          Exosomes are lipid-bilayer-enclosed extracellular vesicles that contain proteins and nucleic acids. They are secreted by all cells and circulate in the blood. Specific detection and isolation of cancer-cell-derived exosomes in the circulation is currently lacking. Using mass spectrometry analyses, we identify a cell surface proteoglycan, glypican-1 (GPC1), specifically enriched on cancer-cell-derived exosomes. GPC1(+) circulating exosomes (crExos) were monitored and isolated using flow cytometry from the serum of patients and mice with cancer. GPC1(+) crExos were detected in the serum of patients with pancreatic cancer with absolute specificity and sensitivity, distinguishing healthy subjects and patients with a benign pancreatic disease from patients with early- and late-stage pancreatic cancer. Levels of GPC1(+) crExos correlate with tumour burden and the survival of pre- and post-surgical patients. GPC1(+) crExos from patients and from mice with spontaneous pancreatic tumours carry specific KRAS mutations, and reliably detect pancreatic intraepithelial lesions in mice despite negative signals by magnetic resonance imaging. GPC1(+) crExos may serve as a potential non-invasive diagnostic and screening tool to detect early stages of pancreatic cancer to facilitate possible curative surgical therapy.
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            Extracellular Vesicles in Cancer: Cell-to-Cell Mediators of Metastasis.

            Tumor-secreted extracellular vesicles (EVs) are critical mediators of intercellular communication between tumor cells and stromal cells in local and distant microenvironments. Accordingly, EVs play an essential role in both primary tumor growth and metastatic evolution. EVs orchestrate multiple systemic pathophysiological processes, such as coagulation, vascular leakiness, and reprogramming of stromal recipient cells to support pre-metastatic niche formation and subsequent metastasis. Clinically, EVs may be biomarkers and novel therapeutic targets for cancer progression, particularly for predicting and preventing future metastatic development.
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              Challenges and directions in studying cell–cell communication by extracellular vesicles

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                Author and article information

                Contributors
                Journal
                Front Bioinform
                Front Bioinform
                Front. Bioinform.
                Frontiers in Bioinformatics
                Frontiers Media S.A.
                2673-7647
                09 February 2023
                2023
                : 3
                : 1117271
                Affiliations
                Guangzhou Laboratory , Guangzhou, China
                Author notes

                Edited by: Qi Zhao, University of Science and Technology Liaoning, China

                Reviewed by: Qingshi Wang, University of Alabama, United States

                *Correspondence: Yixue Li, yxli@ 123456sibs.ac.cn ; Tao Zeng, zeng_tao@ 123456gzlab.ac.cn

                This article was submitted to Integrative Bioinformatics, a section of the journal Frontiers in Bioinformatics

                Article
                1117271
                10.3389/fbinf.2023.1117271
                9947558
                36844931
                9ba2b418-1090-4e6b-9871-c2066ed96d3d
                Copyright © 2023 Liu, Li and Zeng.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 06 December 2022
                : 31 January 2023
                Funding
                This paper was supported by the National Key R&D Program of China (No. 2022YFF1202100), the National Natural Science Foundation of China (No. 11871456), and the Shanghai Municipal Science and Technology Major Project (Grant No. 2017SHZDZX01).
                Categories
                Bioinformatics
                Perspective

                extracellular vesicles,multi-omics,integration,lung disease,integrative bioinformatics

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