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EWI‐2 controls nucleocytoplasmic shuttling of EGFR signaling molecules and miRNA sorting in exosomes to inhibit prostate cancer cell metastasis

机译:EWI-2控制EGFR信号分子的核细胞骨质穿梭并在外泌体中分选以抑制前列腺癌细胞转移

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摘要

Early and accurate diagnosis of prostate cancer (PCa) is extremely important, as metastatic PCa remains hard to treat. EWI‐2, a member of the Ig protein subfamily, is known to inhibit PCa cell migration. In this study, we found that EWI‐2 localized on both the cell membrane and exosomes regulates the distribution of miR‐3934‐5p between cells and exosomes. Interestingly, we observed that EWI‐2 is localized not only on the plasma membrane but also on the nuclear envelope (nuclear membrane), where it regulates the nuclear translocation of signaling molecules and miRNA. Collectively, these functions of EWI‐2 found in lipid bilayers appear to regulate PCa cell metastasis through the epidermal growth factor receptor‐mitogen‐activated protein kinase‐extracellular‐signal‐regulated kinase (EGFR‐MAPK‐ERK) pathway. Our research provides new insights into the molecular function of EWI‐2 on PCa metastasis, and highlights EWI‐2 as a potential PCa biomarker.
机译:早期和准确地诊断前列腺癌(PCA)非常重要,因为转移性PCA难以治疗。已知EWI-2,IG蛋白质亚家族的成员抑制PCA细胞迁移。在这项研究中,我们发现EWI-2在细胞膜和外泌体上局部地调节细胞和外泌体之间miR-3934-5p的分布。有趣的是,我们观察到EWI-2不仅在质膜上本地化,而且在核封膜(核膜)上,在那里调节信号传导分子和miRNA的核转移。集体,在脂质双层中发现的EWI-2功能似乎通过表皮生长因子受体 - 丝裂剂激活蛋白激酶 - 细胞外信号调节激酶(EGFR-MAPK-ERK)途径调节PCA细胞转移。我们的研究为EWI-2对PCA转移的分子功能提供了新的见解,并将EWI-2突出显示为潜在的PCA生物标志物。

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