## Abstract Nasopharyngeal carcinoma is closely associated with Epstein‐Barr virus (EBV) and the EBV encoded latent membrane protein‐1 expression (LMP1) is commonly found in the tumour cells. LMP1 has been shown to be involved in modulation of cell growth in B cells but the biological properties of
Upregulation of interleukin-1 by Epstein–Barr virus latent membrane protein 1 and its possible role in nasopharyngeal carcinoma cell growth
✍ Scribed by Yu-Tzu Huang; Mei-Ying Liu; Ching-Hwa Tsai; Te-Huei Yeh
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 273 KB
- Volume
- 32
- Category
- Article
- ISSN
- 1043-3074
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✦ Synopsis
Abstract
Background
Nasopharyngeal carcinoma (NPC) is associated with Epstein–Barr virus (EBV) infection. We previously found that interleukin (IL)‐1α and IL‐1β significantly increased in NPC tissues. This study investigated what EBV‐encoded proteins were involved in such IL‐1 production.
Methods and Results
IL‐1α and IL‐1β messenger ribonucleic acids (mRNAs) were detected in the EBV latent membrane protein 1 (LMP1) transfectant (LMP135) only by reverse transcriptase–polymerase chain reaction (RT‐PCR). LMP1‐mediated IL‐1α and IL‐1β production could be enhanced by tumor necrosis factor alpha (TNF‐α), determined by enzyme‐linked immunosorbent assay (ELISA). Moreover, IL‐1α and IL‐1β mRNAs and proteins were increased in a dose‐dependent manner in epithelial cells transiently transfected by an LMP1 plasmid. Besides, immortalized human epidermal keratinocyte (RHEK‐1) epithelial cells could be enhanced to proliferate by IL‐1α and IL‐1β determined by water‐soluble tetrazolium salt (WST‐1) assay.
Conclusions
EBV LMP1 is capable of upregulating IL‐1α and IL‐1β secretions from epithelial cells and positively modulated by TNF‐α. This may consequently contribute to tumor growth in patients with NPC. © 2009 Wiley Periodicals, Inc. Head Neck, 2009
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We reported previously that a characteristic Epstein-Barr virus latent membrane protein 1 (EBV-LMP1) gene was associated with nasopharyngeal carcinoma (NPC) in Hong Kong. It showed a 30 bp deletion at the carboxyl terminus with specific amino acid substitution Asp at codon 335 with reference to Gly
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