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   <subfield code="a">Satellite non-coding RNAs: the emerging players in cells, cellular pathways and cancer</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Daniela Ferreira, Susana Meles, Ana Escudeiro, Ana Mendes-da-Silva, Filomena Adega, Raquel Chaves]</subfield>
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   <subfield code="a">For several decades, transcriptional inactivity was considered as one of the particular features of constitutive heterochromatin and, therefore, of its major component, satellite DNA sequences. However, more recently, succeeding evidences have demonstrated that these sequences can indeed be transcribed, yielding satellite non-coding RNAs with important roles in the organization and regulation of genomes. Since then, several studies have been conducted, trying to understand the function(s) of these sequences not only in the normal but also in cancer genomes. It is thought that the association between cancer and satncRNAs is mostly due to the influence of these transcripts in the genome instability, a hallmark of cancer. The few reports on satellite DNA transcription in cancer contexts point to its overexpression; however, this scenario may be far more complex, variable, and influenced by a number of factors andthe exact role of satncRNAs in the oncogenic process remains poorly understood. The greater is the knowledge on the association of satncRNAs with cancer, the greater would be the opportunity to assist cancer treatment, either by the design of effective therapies targeting these molecules or by using them as biomarkers in cancer diagnosis, prognosis, and with predictive value.</subfield>
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   <subfield code="a">Springer Science+Business Media Dordrecht, 2015</subfield>
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   <subfield code="a">Satellite DNA</subfield>
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   <subfield code="a">Satellite non-coding RNA</subfield>
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   <subfield code="a">Cancer</subfield>
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   <subfield code="a">Biomarkers</subfield>
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   <subfield code="a">Genomic instability</subfield>
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   <subfield code="a">ChIP : Chromatin immunoprecipitation</subfield>
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   <subfield code="a">CPC : Chromosome passenger complex</subfield>
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   <subfield code="a">CT : Centromeric</subfield>
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   <subfield code="a">dTALEs : Designer transcription activator-like effectors</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">HP1 : Heterochromatin protein 1</subfield>
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   <subfield code="a">HSF1 : Heat shock factor 1</subfield>
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   <subfield code="a">lncRNAs : Long non-coding RNAs</subfield>
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   <subfield code="a">mRNAs : Messenger RNAs</subfield>
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   <subfield code="a">ncRNAs : Non-coding RNAs</subfield>
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   <subfield code="a">ORF : Open reading frame</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">PCT : Pericentromeric</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">RIP : RNA immunoprecipitation</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">RNA-FISH : RNA fluorescence in situ hybridization</subfield>
   <subfield code="2">nationallicence</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">RT-qPCR : Reverse transcriptase quantitative polymerase chain reaction</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">satDNA : Satellite DNA</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">satncRNAs : Satellite non-coding RNAs</subfield>
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   <subfield code="a">siRNAs : Small interfering RNAs</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">TonEBF : Tonicity enhancer-binding protein</subfield>
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  <datafield tag="690" ind1=" " ind2="7">
   <subfield code="a">TRAIN : Transcription of repeats activates interferon</subfield>
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   <subfield code="a">Ferreira</subfield>
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   <subfield code="a">Meles</subfield>
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   <subfield code="t">Chromosome Research</subfield>
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   <subfield code="a">Metadata rights reserved</subfield>
   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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