: Highly tumorigenic lung cancer CD133+ cells display stem-like features and are spared by cisplatin treatment. Proc Natl Acad Sci U S A 2009, 106:16281–16286.PubMedCrossRef 53. Rizzo S, Hersey JM, Mellor P, Dai W, Santos-Silva A, Liber D, Luk L, Titley I, Carden CP, Box G, et al.: Ovarian cancer stem cell-like side populations are enriched following chemotherapy and overexpress EZH2. Mol Cancer Ther 2011, 10:325–335.PubMedCrossRef Competing interests The authors state no competing interests. Authors’ contributions GS and AE conceived and designed

the study. AE wrote the paper and GS contributed to the writing and to the critical reading of the paper. GS, KF, VS and FL performed click here the experiments. EP and ED provided patient

samples and performed the immunohistochemistry. MB performed the flow cytometry analysis. LM, AP and DM contributed to the genetic characterization of melanospheres. MM contributed to critically revise the manuscript. RDM gave a key contribution to the intellectual content of the study. All authors read and approved the final manuscript.”
“Introduction Epstein-Barr virus (EBV) is a ubiquitous herpes virus that is linked to multiple malignancies, including Burkitt’s lymphoma, Hodgkin’s disease, gastric cancer esophageal cancer cervical cancer and prostate cancer and nasopharyngeal carcinoma (NPC) [1–9]. Latent membrane protein 1 (LMP1) encoded by EBV functions as an essential factor in EBV-induced cell transformation and is expressed in many of the malignancies associated with EBV. LMP1 protein is detected in approximately 60 percent of tissue

samples from patients with buy OICR-9429 Urease NPC [10, 11], while LMP1 mRNA is detected in nasopharyngeal swabs in over 90% of NPC patients by RT-PCR [12, 13]. The frequent expression of LMP1 in undifferentiated NPC points to a role for this viral oncoprotein as a key molecule in NPC pathogenesis [14–19]. Elevated amounts of the epidermal growth factor receptor (EGFR) at both the protein and mRNA levels are detected in the DZNeP epithelial cell carcinomas including NPC, and its expression correlates with the levels of LMP1 [20]. Our earlier research reports that LMP1 may increase both expression and phosphorylation levels of EGFR [21, 22] and that LMP1 could regulate the nuclear accumulation of EGFR in a dose-dependent manner quantitatively and qualitatively [23]. We also showed that nuclear EGFR could bind to the cyclin D1 promoter directly and transactivate the cyclin D1 promoter by LMP1 in NPC. Many factors such as the epidermal growth factor, the DNA damage factor, ultraviolet irradiation, radiation and cetuximab increase EGFR translocation into the nucleus [24–29]. These findings clearly indicate that EGFR may act as a new factor that directly target genes related to cellular transformation, cell cycle regulation, DNA damage repair and replication.