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Platelets and tumor-associated RNA transfer

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BLOOD
卷 137, 期 23, 页码 3181-3191

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AMER SOC HEMATOLOGY
DOI: 10.1182/blood.2019003978

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  1. European Union's Horizon 2020 Research and Innovation Program under Marie Sklodowska-Curie grant [765492]

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The nucleic acid content of platelets was previously thought to be solely determined by their progenitor cells, but recent research shows that other mediators like cancer cells can influence platelet RNA repertoire. This transfer of RNA from cancer cells to platelets could serve as a novel source of potential biomarkers for early cancer detection and treatment monitoring.
Until recently, the nucleic acid content of platelets was considered to be fully determined by their progenitor megakaryocyte. However, it is now well understood that additional mediators (eg, cancer cells) can intervene, thereby influencing the RNA repertoire of platelets. Platelets are highly dynamic cells that are able to communicate and influence their environment. For instance, platelets have been involved in various steps of cancer development and progression by supporting tumor growth, survival, and dissemination. Cancer cells can directly and/or indirectly influence platelet RNA content, resulting in tumor-mediated education of platelets. Alterations in the tumor-educated platelet RNA profile have been described as a novel source of potential biomarkers. Individual platelet RNA biomarkers as well as complex RNA signatures may be used for early detection of cancer and treatment monitoring. Here, we review the RNA transfer occurring between cancer cells and platelets. We explore the potential use of platelet RNA biomarkers as a liquid biopsy biosource and discuss methods to evaluate the transcriptomic content of platelets.

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