Estrogen induces the expression of EBV lytic protein ZEBRA, a marker of poor prognosis in nasopharyngeal carcinoma.
Hirotomo DochiSatoru KondoTakayuki MurataMasaki FukuyoAsuka NanboKousho WakaeWen-Ping JiangToshihide Hamabe-HoriikeMariko TanakaTakumi NishiuchiHarue MizokamiMakiko Moriyama-KitaEiji KobayashiNobuyuki HiraiTakeshi KomoriTakayoshi UenoYosuke NakanishiMiyako HatanoKazuhira EndoHisashi SugimotoNaohiro WakisakaShin-Hun JuangMasamichi MuramatsuAtsushi KanedaTomokazu YoshizakiPublished in: Cancer science (2022)
Several epidemiological studies have suggested that Epstein-Barr virus (EBV) lytic infection is essential for the development of nasopharyngeal carcinoma (NPC), as the elevation of antibody titers against EBV lytic proteins is a common feature of NPC. Although ZEBRA protein is a key trigger for the initiation of lytic infection, whether its expression affects the prognosis and pathogenesis of NPC remains unclear. In this study, 64 NPC biopsy specimens were analyzed using immunohistochemistry. We found that ZEBRA was significantly associated with a worsening of progression-free survival in NPC (adjusted hazard ratio, 3.58; 95% confidence interval, 1.08-11.87; p = 0.037). Moreover, ZEBRA expression positively correlated with key endocrinological proteins, estrogen receptor α, and aromatase. The transcriptional level of ZEBRA is activated by estrogen in an estrogen receptor α-dependent manner, resulting in an increase in structural gene expression levels and extracellular virus DNA copy number in NPC cell lines, reminiscent of lytic infection. Interestingly, it did not suppress cellular proliferation or increase apoptosis, in contrast with cells treated with 12-O-tetradecanoylphorbol-13-acetate and sodium butyrate, indicating that viral production induced by estrogen is not a cell lytic phenomenon. Our results suggest that intratumoral estrogen overproduced by aromatase could induce ZEBRA expression and EBV reactivation, contributing to the progression of NPC.
Keyphrases
- estrogen receptor
- poor prognosis
- epstein barr virus
- long non coding rna
- diffuse large b cell lymphoma
- gene expression
- copy number
- binding protein
- dna methylation
- cell cycle arrest
- mitochondrial dna
- sars cov
- induced apoptosis
- single cell
- oxidative stress
- signaling pathway
- stem cells
- magnetic resonance imaging
- endoplasmic reticulum stress
- machine learning
- cell death
- cell therapy
- ultrasound guided
- cell free
- cell proliferation
- computed tomography
- amino acid
- protein protein
- fine needle aspiration
- deep learning
- single molecule