r knowledge, this is the first miRNA profile of EBV-positive NK/T-cell lymphoma, T-cell lymphoma and normal thymus tissue established by deep sequencing of small RNA libraries as NK/T-cell MedChemExpress 5-Carboxy-X-rhodamine lymphomas are virtually always EBVpositive. Therefore, we used EBV-negative T-cell lymphoma for comparison. Two previous publications described a miRNA analysis of thymus tissue. The paper by Liang et al. used a PCR-based method to evaluate miRNA levels in various normal human tissues including thymus. In their analysis, as in ours, miR-16 was one of the predominantly expressed miRNAs. Using miR-16 for normalization, we compared the values for the thymus tissues for those miRNAs that were deregulated in our lymphomas. We found that their data matched ours for some but not all miRNAs. The publication by Barad et al. used a micro array analysis of five normal human tissues including thymus and reported for thymus that miR-96, -182, -183 and 200a showed the strongest expression of all miRNAs tested. These miRNAs were present in the thymus small RNA library analysed here but did not represent highly expressed miRNAs. We The Differentially Expressed miR-205 Targets the Oncogene BCL6 MiRNA Profile of EBV-Positive NK/T-Cell Lymphoma assume that the different methods used were responsible for the observed discrepancies. When this analysis 
was designed, the nature of the nonneoplastic precursor cells of the NK/T-cell lymphoma was still a matter of debate. We therefore chose to analyse thymus tissue as a non-transformed control tissue known to be involved in NK/T-cell development. It is assumed today that most NK/ T-cell lymphomas are derived from CD56+ NK cells or occasionally from cytotoxic T-cells. Recently, Ng et al. analysed the miRNA levels of nasal NK/T-cell lymphoma and a panel of NK/T-cell lines in comparison to CD56+ precursor cells by an array-based technology. They observed a general down-regulation of cellular miRNAs with only a few up-regulated miRNAs of most miRNAs analysed. Our data confirm these results in that we observe a general repression of miRNA expression as demonstrated by the reduced relative number of miRNA counts in the library of the EBV+-NK/T-cell lymphoma in line with our previous analyses of such libraries obtained for EBV-positive nasopharyngeal carcinoma and diffuse PubMed ID:http://www.ncbi.nlm.nih.gov/pubmed/22203538 large B-cell lymphoma . Other publications have also described a global repression of miRNAs in tumours and that this repression can enhance tumorigenesis. One of the miRNAs which showed a reduced expression in both EBV-positive NK/T-cell lymphoma as well as the EBV-negative T-cell lymphomas was miR-218. The repression of miR-218 was already described for gastric carcinoma and shown to function as an inhibitor of invasion and metastasis. Furthermore, the reduction of miR-218 was associated with strong activation of NFkB which is also often seen in NK/T-cell lymphoma. The paper by Ng et al did not report a change in expression for miR-218, though. In the EBV-negative lymphomas, the members of the miR-200 family were not expressed or showed only a very low expression. For most of them, the expression was also reduced in EBV-positive lymphomas compared to thymus; only miR-200b and miR-141 were slightly above the two-fold reduction. The repression of these miRNAs coincides with publications showing that the down-regulation of miR-200 family contributes to metastasis of tumour cells by targeting ZEB1/ZEB2 and increasing E-cadherin. MiR-424 and -128a+b were significantly
