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10.1002/embr.201337950 http://scihub22266oqcxt.onion/10.1002/embr.201337950 C3989671!3989671 !24534129     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=24534129 &cmd=llinks): Failed to open stream: HTTP request failed! 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The expression level of small non-coding RNAs derived from the first exon of protein-coding genes is predictive of cancer status |pdf=|usr=}}{{24534129 }} gab.com Text The expression level of small non-coding RNAs derived from the first exon of protein-coding genes is predictive of cancer status JO: EMBO Rep http://www.kidney.de/pget.php?&tw=1&pmid=24534129 #FOAvip Small non-coding RNAs (smRNAs) are known to be significantly enriched near the transcriptional start sites of genes. However, the functional relevance of these smRNAs remains unclear, and they have not been associated with human disease. Within the cancer genome atlas project (TCGA), we have generated small RNA datasets for many tumor types. In prior cancer studies, these RNAs have been regarded as transcriptional "noise," due to their apparent chaotic distribution. In contrast, we demonstrate their striking potential to distinguish efficiently between cancer and normal tissues and classify patients with cancer to subgroups of distinct survival outcomes. This potential to predict cancer status is restricted to a subset of these smRNAs, which is encoded within the first exon of genes, highly enriched within CpG islands and negatively correlated with DNA methylation levels. Thus, our data show that genome-wide changes in the expression levels of small non-coding RNAs within first exons are associated with cancer. Twit Text FOAVip The expression level of small non-coding RNAs derived from the first exon of protein-coding genes is predictive of cancer status ????EMBO Rep http://www.kidney.de/pget.php?&tw=1&pmid=24534129 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24534129 #FOAvip English Wikipedia <ref>{{Cite pmid|24534129 }}</ref> The expression level of small non-coding RNAs derived from the first exon of protein-coding genes is predictive of cancer status #MMPMID24534129 Zovoilis A ; Mungall AJ ; Moore R ; Varhol R ; Chu A ; Wong T ; Marra M ; Jones SJ EMBO Rep 2014[Apr]; 15 (4 ): 402-10 PMID24534129 show ga Small non-coding RNAs (smRNAs) are known to be significantly enriched near the transcriptional start sites of genes. However, the functional relevance of these smRNAs remains unclear, and they have not been associated with human disease. Within the cancer genome atlas project (TCGA), we have generated small RNA datasets for many tumor types. In prior cancer studies, these RNAs have been regarded as transcriptional "noise," due to their apparent chaotic distribution. In contrast, we demonstrate their striking potential to distinguish efficiently between cancer and normal tissues and classify patients with cancer to subgroups of distinct survival outcomes. This potential to predict cancer status is restricted to a subset of these smRNAs, which is encoded within the first exon of genes, highly enriched within CpG islands and negatively correlated with DNA methylation levels. Thus, our data show that genome-wide changes in the expression levels of small non-coding RNAs within first exons are associated with cancer. |Breast Neoplasms/*genetics/metabolism/mortality [MESH] |Carcinoma, Ductal, Breast/*genetics/metabolism/mortality [MESH] |CpG Islands [MESH] |DNA Methylation [MESH] |Exons [MESH] |Female [MESH] |Gene Expression [MESH] |Gene Expression Regulation, Neoplastic [MESH] |Humans [MESH] |Open Reading Frames [MESH] |RNA, Messenger/genetics/metabolism [MESH] |RNA, Small Untranslated/genetics/*metabolism [MESH] |Sequence Analysis, DNA [MESH] |Survival Analysis [MESH] |Transcription Initiation Site [MESH]The expression level of small non-coding RNAs derived from the first e(epmc).pdf DeepDyve Pubget Overpricing