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

**Authors:** Haiping Liu, Juan Wang, Lin Wang, Wei Tang, Xinyue Hou, Yi Zhun Zhu, Xu Chen

PMC · DOI: 10.3390/biom14091142 · 2024-09-09

## TL;DR

This study explores how curcumol, a compound from a traditional Chinese herb, reduces the spread of nasopharyngeal carcinoma by targeting specific proteins linked to EBV infection.

## Contribution

The paper introduces a multi-omics approach to uncover how curcumol inhibits NCL/EBNA1-mediated UBE2C upregulation in EBV-positive NPC.

## Key findings

- Curcumol treatment significantly affects ubiquitin-mediated proteolysis and cell cycle pathways in NPC cells.
- UBE2C is highly associated with GABA and plays a key role in curcumol resistance in EBV-positive NPC.
- NCL and EBNA1 are critical in mediating curcumol resistance to NPC invasion and metastasis.

## Abstract

Nasopharyngeal carcinoma (NPC) is closely linked to Epstein–Barr virus (EBV) infection. Curcumae Rhizoma, 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.

## Linked entities

- **Genes:** NUCLEOLIN (nucleolin multifunctional protein) [NCBI Gene 4691], EBNA-1 (protein-coding) [NCBI Gene 3783709], UBE2C (ubiquitin conjugating enzyme E2 C) [NCBI Gene 11065]
- **Proteins:** NUCLEOLIN (nucleolin multifunctional protein)
- **Chemicals:** curcumol (PubChem CID 14240392), 4-Aminobutanoic acid (PubChem CID 119), GABA (PubChem CID 119)
- **Diseases:** nasopharyngeal carcinoma (MONDO:0015459), Nasopharyngeal carcinoma (MONDO:0015459)

## Full-text entities

- **Genes:** NUCLEOLIN (nucleolin multifunctional protein) [NCBI Gene 4691] {aka C23, NCL, Nsr1}, AKT1 (AKT serine/threonine kinase 1) [NCBI Gene 207] {aka AKT, PKB, PKB-ALPHA, PRKBA, RAC, RAC-ALPHA}, UBE2C (ubiquitin conjugating enzyme E2 C) [NCBI Gene 11065] {aka UBCH10, dJ447F3.2}, EBNA1 [NCBI Gene 17494214], MTOR (mechanistic target of rapamycin kinase) [NCBI Gene 2475] {aka FRAP, FRAP1, FRAP2, RAFT1, RAPT1, SKS}
- **Diseases:** complement and coagulation (MESH:D001778), NPC (MESH:D000077274), tumor (MESH:D009369), and Metastasis (MESH:D009362), EBV-positive NPC (MESH:D020031)
- **Cell lines:** C666-1 — Homo sapiens (Human), Nasopharyngeal carcinoma, Cancer cell line (CVCL_7949)

## Figures

11 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11430640/full.md

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Source: https://tomesphere.com/paper/PMC11430640