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YBX3介导鼻咽癌的转移及PI3K/AKT信号传导。

YBX3 Mediates the Metastasis of Nasopharyngeal Carcinoma PI3K/AKT Signaling.

作者信息

Fan Xiaoqin, Xie Xina, Yang Ming, Wang Yujie, Wu Hanwei, Deng Tingting, Weng Xin, Wen Weiping, Nie Guohui

机构信息

Department of Otolaryngology, The First Affiliated Hospital of Sun Yat-Sen University, Guangzhou, China.

Department of Otolaryngology, Shenzhen Second People's Hospital, The First Affiliated Hospital of Shenzhen University, Shenzhen, China.

出版信息

Front Oncol. 2021 Mar 17;11:617621. doi: 10.3389/fonc.2021.617621. eCollection 2021.

Abstract

The metastasis of nasopharyngeal carcinoma (NPC) is a complex process associated with oncogenic dysfunction, the deciphering of which remains a challenge and requires more in-depth studies. Y-box protein 3 (YBX3) is a DNA/RNA binding protein associated with gene transcription, DNA repair, and the progression of various diseases. However, whether and how YBX3 affects the metastasis of NPC remains unknown. Thus, in this study, we aimed to investigate the role of YBX3 in the metastasis of NPC and determine its underlying mechanism. Interestingly, it was found that the expression of YBX3, which was associated with NPC metastasis, was upregulated in the clinical NPC tissues and cell lines. Moreover, we found that knockdown of YBX3 expression by lentivirus shRNA significantly suppressed NPC cells migration and metastasis Mechanistically, RNA sequencing results suggested that the genes regulated by YBX3 were significantly enriched in cell adhesion molecules, cAMP signaling pathway, calcium signaling pathway, focal adhesion, PI3K/AKT signaling pathway, Ras signaling pathway, Rap1 signaling pathway, NF-κB signaling pathway, and Chemokine signaling pathway. Of these, PI3K/AKT signaling pathway contained the most genes. Accordingly, YBX3 knockdown decreased the activation of PI3K/AKT signaling pathway, thereby inhibit epithelial-to-mesenchymal transition (EMT) and MMP1. These results have demonstrated that YBX3 are involved in the metastasis of NPC through regulating PI3K/AKT signaling pathway, and serve as a potential therapeutic target for patients with NPC.

摘要

鼻咽癌(NPC)的转移是一个与致癌功能障碍相关的复杂过程,对其机制的解读仍然是一项挑战,需要更深入的研究。Y盒蛋白3(YBX3)是一种与基因转录、DNA修复以及各种疾病进展相关的DNA/RNA结合蛋白。然而,YBX3是否以及如何影响NPC的转移仍不清楚。因此,在本研究中,我们旨在探讨YBX3在NPC转移中的作用,并确定其潜在机制。有趣的是,我们发现与NPC转移相关的YBX3在临床NPC组织和细胞系中的表达上调。此外,我们发现通过慢病毒shRNA敲低YBX3表达可显著抑制NPC细胞的迁移和转移。从机制上讲,RNA测序结果表明,受YBX3调控的基因在细胞粘附分子、cAMP信号通路、钙信号通路、粘着斑、PI3K/AKT信号通路、Ras信号通路、Rap1信号通路、NF-κB信号通路和趋化因子信号通路中显著富集。其中,PI3K/AKT信号通路包含的基因最多。相应地,敲低YBX3可降低PI3K/AKT信号通路的激活,从而抑制上皮-间质转化(EMT)和基质金属蛋白酶1(MMP1)。这些结果表明,YBX3通过调节PI3K/AKT信号通路参与NPC的转移,并可作为NPC患者潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8889/8010247/6e0d45752a5f/fonc-11-617621-g001.jpg

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