Characterization of the Merkel Cell Carcinoma miRNome

MicroRNAs have been implicated in various skin cancers, including melanoma, squamous cell carcinoma, and basal cell carcinoma; however, the expression of microRNAs and their role in Merkel cell carcinoma (MCC) have yet to be explored in depth. To identify microRNAs specific to MCC (MCC-miRs), next-g...

Full description

Saved in:
Bibliographic Details
Main Authors: Matthew S. Ning, Annette S. Kim, Nripesh Prasad, Shawn E. Levy, Huiqiu Zhang, Thomas Andl
Format: Article
Language:English
Published: Wiley 2014-01-01
Series:Journal of Skin Cancer
Online Access:http://dx.doi.org/10.1155/2014/289548
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1832551656301002752
author Matthew S. Ning
Annette S. Kim
Nripesh Prasad
Shawn E. Levy
Huiqiu Zhang
Thomas Andl
author_facet Matthew S. Ning
Annette S. Kim
Nripesh Prasad
Shawn E. Levy
Huiqiu Zhang
Thomas Andl
author_sort Matthew S. Ning
collection DOAJ
description MicroRNAs have been implicated in various skin cancers, including melanoma, squamous cell carcinoma, and basal cell carcinoma; however, the expression of microRNAs and their role in Merkel cell carcinoma (MCC) have yet to be explored in depth. To identify microRNAs specific to MCC (MCC-miRs), next-generation sequencing (NGS) of small RNA libraries was performed on different tissue samples including MCCs, other cutaneous tumors, and normal skin. Comparison of the profiles identified several microRNAs upregulated and downregulated in MCC. For validation, their expression was measured via qRT-PCR in a larger group of MCC and in a comparison group of non-MCC cutaneous tumors and normal skin. Eight microRNAs were upregulated in MCC: miR-502-3p, miR-9, miR-7, miR-340, miR-182, miR-190b, miR-873, and miR-183. Three microRNAs were downregulated: miR-3170, miR-125b, and miR-374c. Many of these MCC-miRs, the miR-183/182/96a cistron in particular, have connections to tumorigenic pathways implicated in MCC pathogenesis. In situ hybridization confirmed that the highly expressed MCC-miR, miR-182, is localized within tumor cells. Furthermore, NGS and qRT-PCR reveal that several of these MCC-miRs are highly expressed in the patient-derived MCC cell line, MS-1. These data indicate that we have identified a set of MCC-miRs with important implications for MCC research.
format Article
id doaj-art-2bc582de855d48b78b89fe30c974b437
institution Kabale University
issn 2090-2905
2090-2913
language English
publishDate 2014-01-01
publisher Wiley
record_format Article
series Journal of Skin Cancer
spelling doaj-art-2bc582de855d48b78b89fe30c974b4372025-02-03T06:00:53ZengWileyJournal of Skin Cancer2090-29052090-29132014-01-01201410.1155/2014/289548289548Characterization of the Merkel Cell Carcinoma miRNomeMatthew S. Ning0Annette S. Kim1Nripesh Prasad2Shawn E. Levy3Huiqiu Zhang4Thomas Andl5Division of Dermatology, Department of Medicine, Vanderbilt University Medical Center, Medical Center North, Room A2310A, 1161 21st Avenue South, Nashville, TN 37232-2600, USADepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN 37232-2600, USADepartment of Biological Sciences, University of Alabama in Huntsville, Huntsville, AL 35805, USAHudsonAlpha Institute for Biotechnology, Huntsville, AL 35806, USAOrioR Lab, LLC, Rockville, MD 20852, USADivision of Dermatology, Department of Medicine, Vanderbilt University Medical Center, Medical Center North, Room A2310A, 1161 21st Avenue South, Nashville, TN 37232-2600, USAMicroRNAs have been implicated in various skin cancers, including melanoma, squamous cell carcinoma, and basal cell carcinoma; however, the expression of microRNAs and their role in Merkel cell carcinoma (MCC) have yet to be explored in depth. To identify microRNAs specific to MCC (MCC-miRs), next-generation sequencing (NGS) of small RNA libraries was performed on different tissue samples including MCCs, other cutaneous tumors, and normal skin. Comparison of the profiles identified several microRNAs upregulated and downregulated in MCC. For validation, their expression was measured via qRT-PCR in a larger group of MCC and in a comparison group of non-MCC cutaneous tumors and normal skin. Eight microRNAs were upregulated in MCC: miR-502-3p, miR-9, miR-7, miR-340, miR-182, miR-190b, miR-873, and miR-183. Three microRNAs were downregulated: miR-3170, miR-125b, and miR-374c. Many of these MCC-miRs, the miR-183/182/96a cistron in particular, have connections to tumorigenic pathways implicated in MCC pathogenesis. In situ hybridization confirmed that the highly expressed MCC-miR, miR-182, is localized within tumor cells. Furthermore, NGS and qRT-PCR reveal that several of these MCC-miRs are highly expressed in the patient-derived MCC cell line, MS-1. These data indicate that we have identified a set of MCC-miRs with important implications for MCC research.http://dx.doi.org/10.1155/2014/289548
spellingShingle Matthew S. Ning
Annette S. Kim
Nripesh Prasad
Shawn E. Levy
Huiqiu Zhang
Thomas Andl
Characterization of the Merkel Cell Carcinoma miRNome
Journal of Skin Cancer
title Characterization of the Merkel Cell Carcinoma miRNome
title_full Characterization of the Merkel Cell Carcinoma miRNome
title_fullStr Characterization of the Merkel Cell Carcinoma miRNome
title_full_unstemmed Characterization of the Merkel Cell Carcinoma miRNome
title_short Characterization of the Merkel Cell Carcinoma miRNome
title_sort characterization of the merkel cell carcinoma mirnome
url http://dx.doi.org/10.1155/2014/289548
work_keys_str_mv AT matthewsning characterizationofthemerkelcellcarcinomamirnome
AT annetteskim characterizationofthemerkelcellcarcinomamirnome
AT nripeshprasad characterizationofthemerkelcellcarcinomamirnome
AT shawnelevy characterizationofthemerkelcellcarcinomamirnome
AT huiqiuzhang characterizationofthemerkelcellcarcinomamirnome
AT thomasandl characterizationofthemerkelcellcarcinomamirnome