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Tumor-derived exosomes are enriched in ANp73, which promotes oncogenic potential in acceptor cells and correlates with patient survival

机译:肿瘤来源的外泌体富含ANp73,可促进受体细胞中的致癌潜能并与患者存活率相关

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摘要

Tumor-derived exosomes are emerging as local and systemic cell-to-cell mediators of oncogenic information through the horizontal transfer of mRNAs, microRNAs and proteins during tumorigenesis. The exosomal content has been described as biologically active when taken up by the recipient cell. Identifying the specific molecular cargo of exosomes will help to determine their function in specific steps of the tumorigenic process. Here we evaluate whether ANp73 is selectively packaged in tumor-derived exosomes, its function in the acceptor cells in vitro and in vivo and its prognosis potential in cancer. ANp73 messenger is enriched in tumor-derived exosomes, suggesting its active sorting in these microvesicles. We observed the transmission of this exosome cargo to different cell types and how it confers proliferation potential and chemoresistance to the acceptor cells in vitro and in animal models. Finally, our data support the potential prognostic value of exosomal ANp73 in colon cancer patients.
机译:肿瘤来源的外泌体通过在肿瘤发生过程中mRNA,microRNA和蛋白质的水平转移而成为致癌信息的局部和系统性细胞间介体。当被受体细胞吸收时,外泌体含量被描述为具有生物活性。鉴定外泌体的特定分子物质将有助于确定其在致瘤过程的特定步骤中的功能。在这里,我们评估ANp73是否选择性地包装在肿瘤来源的外泌体中,在体外和体内在受体细胞中的功能及其在癌症中的预后。 ANp73信使富含肿瘤来源的外泌体,表明其在这些微囊泡中的活性分选。我们观察到这种外泌体货物向不同细胞类型的传播,以及它如何在体外和动物模型中赋予受体细胞增殖潜能和化学抗性。最后,我们的数据支持外泌体ANp73在结肠癌患者中的潜在预后价值。

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