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miRNA profiling in vitreous humor, vitreal exosomes and serum from uveal melanoma patients: Pathological and diagnostic implications

Journal article
Authors M. Ragusa
C. Barbagallo
L. Statello
R. Caltabiano
A. Russo
L. Puzzo
T. Avitabile
A. Longo
M. D. Toro
D. Barbagallo
Hadi Valadi
C. Di Pietro
M. Purrello
M. Reibaldi
Published in Cancer Biology & Therapy
Volume 16
Issue 9
Pages 1387-1396
ISSN 1538-4047
Publication year 2015
Published at Institute of Medicine, Department of Rheumatology and Inflammation Research
Pages 1387-1396
Language en
Links dx.doi.org/10.1080/15384047.2015.10...
Keywords exosomes, microRNAs, serum, uveal melanoma, vitreous humor, circulating micrornas, cancer, tumor, disease, biomarkers, prognosis, markers, plasma, rnas, cell, oncology
Subject categories Cancer and Oncology

Abstract

Uveal melanoma (UM) represents approximately 5-6% of all melanoma diagnoses and up to 50% of patients succumb to their disease. Although several methods are available, accurate diagnosis is not always easily feasible because of potential accidents (e.g., intraocular hemorrhage). Based on the assumption that the profile of circulating miRNAs is often altered in human cancers, we verified whether UM patients showed different vitreous humor (VH) or serum miRNA profiles with respect to healthy controls. By using TaqMan Low Density Arrays, we analyzed 754 miRNAs from VH, vitreal exosomes, and serum of 6 UM patients and 6 healthy donors: our data demonstrated that the UM VH profile was unique and only partially overlapping with that from serum of the same patients. Whereas, 90% of miRNAs were shared between VH and vitreal exosomes, and their alterations in UM were statistically overlapped with those of VH and vitreal exosomes, suggesting that VH alterations could result from exosomal dysregulation. We report 32 miRNAs differentially expressed in UM patients in at least 2 different types of samples analyzed. We validated these data on an independent cohort of 12 UM patients. Most alterations were common to VH and vitreal exosomes (e.g., upregulation of miR-21,-34 a,-146a). Interestingly, miR-146a was upregulated in the serum of UM patients, as well as in serum exosomes. Upregulation of miR-21 and miR-146a was also detected in formalin-fixed, paraffin-embedded UM, suggesting that VH or serum alterations in UM could be the consequence of disregulation arising from tumoral cells. Our findings suggest the possibility to detect in VH and serum of UM patients diagnostic miRNAs released by the affected eye: based on this, miR-146a could be considered a potential circulating marker of UM.

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Denna text är utskriven från följande webbsida:
http://www.gu.se/english/research/publication/?publicationId=224435
Utskriftsdatum: 2019-11-20