Circular RNA is enriched and stable in exosomes: a promising biomarker for cancer diagnosis
Circular RNAs (circRNAs) are recently identified as a naturally occurring family of widespread and diverse endogenous noncoding RNAs that may regulate gene expression in mammals . They are unusually sta- ble RNA molecules with cell type- or developmental stage-specific expression patterns . Exosomes...
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          | Published in | Cell research Vol. 25; no. 8; pp. 981 - 984 | 
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| Main Authors | , , , , , , , , , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        London
          Nature Publishing Group UK
    
        01.08.2015
     Nature Publishing Group  | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 1001-0602 1748-7838 1748-7838  | 
| DOI | 10.1038/cr.2015.82 | 
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| Summary: | Circular RNAs (circRNAs) are recently identified as a naturally occurring family of widespread and diverse endogenous noncoding RNAs that may regulate gene expression in mammals . They are unusually sta- ble RNA molecules with cell type- or developmental stage-specific expression patterns . Exosomes are small membrane vesicles of endocytic origin secreted by most cell types. They contain a specific cargo of protein, mRNA and microRNA species, which can modulate recipient cell behaviors and may be used as biomarkers for diagnosis of human diseases . | 
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| Bibliography: | 31-1568 Circular RNAs (circRNAs) are recently identified as a naturally occurring family of widespread and diverse endogenous noncoding RNAs that may regulate gene expression in mammals . They are unusually sta- ble RNA molecules with cell type- or developmental stage-specific expression patterns . Exosomes are small membrane vesicles of endocytic origin secreted by most cell types. They contain a specific cargo of protein, mRNA and microRNA species, which can modulate recipient cell behaviors and may be used as biomarkers for diagnosis of human diseases . ObjectType-Article-1 SourceType-Scholarly Journals-1 content type line 14 ObjectType-Feature-2 content type line 23 These two authors contributed equally to this work.  | 
| ISSN: | 1001-0602 1748-7838 1748-7838  | 
| DOI: | 10.1038/cr.2015.82 |