鼻咽癌细胞中的 Aquaporin-3 受 LMP1 下调,从而调节细胞迁移并影响 EBV 潜伏感染。

IF 1.9 4区 医学 Q3 GENETICS & HEREDITY
Virus Genes Pub Date : 2024-10-01 Epub Date: 2024-08-05 DOI:10.1007/s11262-024-02096-1
Jing Li, Duo Shi, Zhiyuan Gong, Wen Liu, Yan Zhang, Bing Luo
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引用次数: 0

摘要

Epstein-Barr 病毒(EBV)感染与鼻咽癌(NPC)的发展密切相关。水蒸发蛋白 3(AQP3)是水蒸发蛋白家族的成员之一,在肿瘤发生发展过程中,尤其是上皮-间质转化过程中发挥着重要作用。本研究发现,EBV 阳性鼻咽癌细胞中 AQP3 的表达量明显低于 EBV 阴性鼻咽癌细胞。Western 印迹和 qRT-PCR 分析表明,LMP1 通过激活 ERK 通路下调 AQP3 的表达。细胞生物学实验证实,AQP3 通过促进鼻咽癌细胞的迁移和增殖来影响肿瘤的发展。此外,AQP3 还能促进 EBV 阳性鼻咽癌细胞裂解 EBV。EBV 通过 LMP1 抑制 AQP3 的表达可能是 EBV 维持潜伏感染诱导肿瘤进展的机制之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Aquaporin-3 is down-regulated by LMP1 in nasopharyngeal carcinoma cells to regulate cell migration and affect EBV latent infection.

Aquaporin-3 is down-regulated by LMP1 in nasopharyngeal carcinoma cells to regulate cell migration and affect EBV latent infection.

Epstein-Barr virus (EBV) infection has a strong correlation with the development of nasopharyngeal carcinoma (NPC). Aquaporin 3 (AQP3), a member of the aquaporin family, plays an important role in tumor development, especially in epithelial-mesenchymal transition. In this study, the expression of AQP3 in EBV-positive NPC cells was significantly lower than that in EBV-negative NPC cells. Western blot and qRT-PCR analysis showed that LMP1 down-regulated the expression of AQP3 by activating the ERK pathway. Cell biology experiments have confirmed that AQP3 affects the development of tumor by promoting cell migration and proliferation in NPC cells. In addition, AQP3 can promote the lysis of EBV in EBV-positive NPC cells. The inhibition of AQP3 expression by EBV through LMP1 may be one of the mechanisms by which EBV maintains latent infection-induced tumor progression.

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来源期刊
Virus Genes
Virus Genes 医学-病毒学
CiteScore
3.30
自引率
0.00%
发文量
76
审稿时长
3 months
期刊介绍: Viruses are convenient models for the elucidation of life processes. The study of viruses is again on the cutting edge of biological sciences: systems biology, genomics, proteomics, metagenomics, using the newest most powerful tools. Huge amounts of new details on virus interactions with the cell, other pathogens and the hosts – animal (including human), insect, fungal, plant, bacterial, and archaeal - and their role in infection and disease are forthcoming in perplexing details requiring analysis and comments. Virus Genes is dedicated to the publication of studies on the structure and function of viruses and their genes, the molecular and systems interactions with the host and all applications derived thereof, providing a forum for the analysis of data and discussion of its implications, and the development of new hypotheses.
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