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基于多组学探讨莪术醇通过抑制 NCL/EBNA1 介导的 UBE2C 上调抑制鼻咽癌侵袭转移的机制

Multi-Omics Exploration of the Mechanism of Curcumol to Reduce Invasion and Metastasis of Nasopharyngeal Carcinoma by Inhibiting NCL/EBNA1-Mediated UBE2C Upregulation.

机构信息

School of Pharmacy, Faculty of Medicine, Macau University of Science and Technology, Macau 999078, China.

Pharmacology Laboratory of Prevention and Treatment of High Incidence of Disease, Guilin Medical University, Guilin 541199, China.

出版信息

Biomolecules. 2024 Sep 9;14(9):1142. doi: 10.3390/biom14091142.

Abstract

Nasopharyngeal carcinoma (NPC) is closely linked to Epstein-Barr virus (EBV) infection. , a traditional Chinese herb, has shown antitumor effects, primarily through its component curcumol (Cur), which has been shown to reduce NPC cell invasion and migration by targeting nucleolin (NCL) and Epstein-Barr Virus Nuclear Antigen 1 (EBNA1). We constructed an EBV-positive NPC cell model using C666-1 cells and performed transcriptomics studies after treatment with curcumol, which revealed a significant enrichment of ubiquitin-mediated proteolysis, the PI3K-AKT and mTOR signaling pathways, cell cycle and apoptosis involved in tumor invasion and migration. To investigate the importance of NCL and EBNA1 in curcumol-resistant EBV-positive NPC, we performed a multi-omics study using short hairpin NCL (shNCL) and shEBNA1 EBV-positive NPC cells, and the proteomics results showed enrichment in complement and coagulation cascades and ubiquitin-mediated proteolysis signaling pathways. Here, we focused on ubiquitin-conjugating enzyme E2C (UBE2C), which plays an important role in the ubiquitin-mediated proteolysis signaling pathway. In addition, metabolomics revealed that UBE2C is highly associated with 4-Aminobutanoic acid (GABA). In vitro studies further validated the function of the key targets, suggesting that UBE2C plays an important role in NCL and EBNA1-mediated curcumol resistance to nasopharyngeal carcinoma invasion and metastasis.

摘要

鼻咽癌(NPC)与 Epstein-Barr 病毒(EBV)感染密切相关。, 一种中药,具有抗肿瘤作用,主要通过其成分姜黄素(Cur)实现,姜黄素已被证明通过靶向核仁蛋白(NCL)和 Epstein-Barr 病毒核抗原 1(EBNA1)来减少 NPC 细胞的侵袭和迁移。我们使用 C666-1 细胞构建了 EBV 阳性 NPC 细胞模型,并在姜黄素处理后进行了转录组学研究,结果显示泛素介导的蛋白水解、PI3K-AKT 和 mTOR 信号通路、细胞周期和凋亡与肿瘤侵袭和迁移密切相关。为了研究 NCL 和 EBNA1 在姜黄素耐药 EBV 阳性 NPC 中的重要性,我们使用短发夹 NCL(shNCL)和 shEBNA1 EBV 阳性 NPC 细胞进行了多组学研究,蛋白质组学结果显示补体和凝血级联以及泛素介导的蛋白水解信号通路富集。在这里,我们重点研究了泛素结合酶 E2C(UBE2C),它在泛素介导的蛋白水解信号通路中起着重要作用。此外,代谢组学表明 UBE2C 与 4-氨基丁酸(GABA)高度相关。体外研究进一步验证了关键靶点的功能,表明 UBE2C 在 NCL 和 EBNA1 介导的姜黄素耐药 NPC 侵袭和转移中发挥重要作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f36a/11430640/8c620b28d02d/biomolecules-14-01142-g001.jpg

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