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ALYREF通过增加NOTCH1 mRNA的稳定性来促进鼻咽癌的转移。

ALYREF promotes the metastasis of nasopharyngeal carcinoma by increasing the stability of NOTCH1 mRNA.

作者信息

Jin Yanan, Yao Jijin, Fu Jianchang, Huang Qitao, Luo Yilin, You Yafei, Zhang Wangjian, Zhong Qian, Xia Tianliang, Xia Liangping

机构信息

VIP Region, State Key Laboratory of Oncology in South China, Guangdong Key Laboratory of Nasopharyngeal Carcinoma Diagnosis and Therapy, Sun Yat-sen University Cancer Center, Guangzhou, Guangdong, PR China.

The Cancer Center of the Fifth Affiliated Hospital of Sun Yat-sen University, Zhuhai, Guangdong, PR China.

出版信息

Cell Death Dis. 2024 Aug 8;15(8):578. doi: 10.1038/s41419-024-06959-1.

Abstract

Approximately 70% of treatment failures in nasopharyngeal carcinoma (NPC) patients are attributed to distant metastasis, yet the underlying mechanisms remain unclear. RNA 5-methylcytosine (m5C) is an emerging regulatory modification that controls gene expression and plays a critical role in tumor progression. However, there is little information on the potential roles of RNA m5C modification in NPC metastasis. In this study, we found that the m5C reader Aly/REF export factor (ALYREF) is significantly upregulated in NPC, whereby its high expression is associated with metastasis and poor prognosis. ALYREF overexpression was found to promote tumor metastasis of NPC cells in vitro and in vivo. Mechanistically, m5C-modified NOTCH1 mRNA was identified as a target of ALYREF. Moreover, ALYREF was found to upregulate NOTCH1 expression by enhancing its RNA stability in an m5C modification-dependent manner, thereby promoting the activation of the NOTCH signaling pathway and facilitating NPC metastasis. Overall, our data reveal the crucial role of ALYREF in NPC metastasis and provide a potential therapeutic target for NPC.

摘要

鼻咽癌(NPC)患者中约70%的治疗失败归因于远处转移,但其潜在机制仍不清楚。RNA 5-甲基胞嘧啶(m5C)是一种新兴的调控修饰,可控制基因表达并在肿瘤进展中起关键作用。然而,关于RNA m5C修饰在NPC转移中的潜在作用的信息很少。在本研究中,我们发现m5C阅读蛋白Aly/REF输出因子(ALYREF)在NPC中显著上调,其高表达与转移和不良预后相关。发现ALYREF过表达在体外和体内均促进NPC细胞的肿瘤转移。机制上,m5C修饰的NOTCH1 mRNA被鉴定为ALYREF的靶标。此外,发现ALYREF以m5C修饰依赖的方式通过增强其RNA稳定性来上调NOTCH1表达,从而促进NOTCH信号通路的激活并促进NPC转移。总体而言,我们的数据揭示了ALYREF在NPC转移中的关键作用,并为NPC提供了一个潜在的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adb0/11310353/6f8c9470087f/41419_2024_6959_Fig1_HTML.jpg

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