PO-379 Novel tumour specific mirna expressed in classical hodgkin lymphoma cell lines
IntroductionMiRNAs are short non coding RNAs involved in post-transcriptional regulation of gene expression that can acquire oncogenic properties in consequence of overexpression or mutations. Tumour genomes undergo global demethylation that triggers genetic instability and activates transcription o...
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Veröffentlicht in: | ESMO open 2018-07, Vol.3 (Suppl 2), p.A170-A170 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | IntroductionMiRNAs are short non coding RNAs involved in post-transcriptional regulation of gene expression that can acquire oncogenic properties in consequence of overexpression or mutations. Tumour genomes undergo global demethylation that triggers genetic instability and activates transcription of sequences normally silenced by methylation. These include the overexpression of tumour specific miRNAs that can deregulate various processes in the malignant cell. Therefore, the aim of the study was to identify aberrantly activated miRNAs in classical Hodgkin lymphoma (cHL).Material and methodsWe have screened NGS small RNA reads (HiSeq 4000 (Illumina); single-end 50 bp seq) of cHL cell lines (n=7) and compared them to non-HL cell lines (n=10) and germinal centre B cell pools (GCB)(n=10) to find yet undescribed miRNAs. High quality reads validated using FastQC and CAP-miRSeq software mapping to the reference genome (GRCh37) (using Bowtie software) not reported as miRNAs before were identified. In order to find miRNAs expressed exclusively in cHL we have moreover compared the sequences in respect to sequence-derived gene expression data from 143 malignant lymphomas generated by the ICGC MMML-Seq consortium (www.icgc.org). Last, the expression of novel miRNAs seemingly specific for cHL was validated by real-time qPCR using custom designed molecular probes (Thermo Fisher Scientific).Results and discussionsSeven novel miRNAs expressed in at least 3/7 cHL cell lines but neither in the non-HL cell lines nor in the GCB cells and observed with a frequency |
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ISSN: | 2059-7029 2059-7029 |
DOI: | 10.1136/esmoopen-2018-EACR25.407 |