Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
10902416 | Cancer Letters | 2014 | 9 Pages |
Abstract
Proteins, RNAs and viruses can be spread through exosomes, therefore transport utilizing these nanovesicles is of the great interest. MiRNAs are common exosomal constituents capable of influencing expression of a variety of target genes. MiRNA signatures of exosomes are unique in cancer patients and differ from those in normal controls. The knowledge about miRNA profiles of tumor-derived exosomes may contribute to better diagnosis, determination of tumor progression and response to treatment, as well as to the development of targeted therapies. We summarize the current knowledge with regard to miRNAs that are found in exosomes derived from tumors, particularly from melanoma.
Keywords
CCND1TLRBMDCsDGCR8TregsMITFEZH2JAK-STATCDK4Cyclin D1ESCRTRUNX3NIKHMC-1KCNMA1histone-lysine N-methyltransferasehuman mast cell lineHspMSCsExosomeBMP4MVBSepithelial to mesenchymal transitionmultivesicular bodiesBiomarkerEMTToll-like receptorMelanomaRISCMesenchymal stem cellsbone marrow-derived cellsRegulatory T cellsRunt-related transcription factor 3Microphthalmia-associated transcription factorphosphatase and tensin homologRNA-Induced Silencing Complexendosomal sorting complexes required for transportmesenchymal to epithelial transitionMETMicroRNAMiRNAHeat shock proteinbone morphogenetic protein 4Ptencyclin-dependent kinase
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Authors
Anna Gajos-Michniewicz, Markus Duechler, Malgorzata Czyz,