<?xml version='1.0' encoding='UTF-8'?><metadata xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:dcterms="http://purl.org/dc/terms/" xmlns="http://dublincore.org/documents/dcmi-terms/"><dcterms:title>Replication Data for: Secretomic analysis of extracellular vesicles originating from polyomavirus-negative and polyomavirus-positive Merkel cell carcinoma cell lines</dcterms:title><dcterms:identifier>https://doi.org/10.18710/USXCRS</dcterms:identifier><dcterms:creator>Konstantinell, Aelita Gloria Virginia</dcterms:creator><dcterms:publisher>DataverseNO</dcterms:publisher><dcterms:issued>2019-05-06</dcterms:issued><dcterms:modified>2019-05-13T09:49:08Z</dcterms:modified><dcterms:description>This dataset is about analyses of two Merkel cell polyomavirus (MCPyV)-negative and two MCPyV–positive Merkel cell lines secretomic proteins.</dcterms:description><dcterms:description>&lt;/p>Abstract: Extracellular vesicles or exosomes constitute an evolutionarily conserved mechanism of intercellular signaling. Exosomes are gaining an increasing amount of attention due to their role&#xd;
in pathologies, including malignancy, their importance as prognostic and diagnostic markers,&#xd;
and their potential as a therapeutic tool. Merkel cell carcinoma (MCC) is an aggressive form of&#xd;
skin cancer with a poor prognosis. Because an effective systemic treatment for this cancer type&#xd;
is currently not available, an exosome-based therapy was proposed. However, comprehensive&#xd;
secretome profiling has not been performed for MCC. To help unveil the putative contribution&#xd;
of exosomes in MCC, we studied the protein content of MCC-derived exosomes. Since approximately&#xd;
80% of all MCC cases contain Merkel cell polyomavirus (MCPyV), the secretomes of&#xd;
two MCPyV-negative and two MCPyV-positive MCC cell lines were compared. We identified&#xd;
with high confidence 164 exosome-derived proteins common for all four cell lines that were annotated&#xd;
in ExoCarta and Vesiclepedia databases. These include proteins implicated in motility,&#xd;
metastasis and tumor progression, such as integrins and tetraspanins, intracellular signaling&#xd;
molecules, chaperones, proteasomal proteins, and translation factors. Additional virus-negative&#xd;
and virus-positiveMCC cell lines should be examined to identify highly representative exosomal&#xd;
proteins that may provide reliable prognostic and diagnostic biomarkers, as well as targets for&#xd;
treatment in the future. Data are available via ProteomeXchange with identifier PXD004198.</dcterms:description><dcterms:subject>Medicine, Health and Life Sciences</dcterms:subject><dcterms:subject>Merkel cell carcinoma</dcterms:subject><dcterms:subject>Merkel cell polyomavirus</dcterms:subject><dcterms:subject>Exosome</dcterms:subject><dcterms:subject>Proteomics</dcterms:subject><dcterms:isReferencedBy>A. Konstantinell, et al. Secretomic analysis of extracellular vesicles originating from polyomavirus-negative and polyomavirus-positive Merkel cell carcinoma cell lines. Proteomics 2016, 16, 2587-2591., doi, 10.1002/pmic.201600223, https://doi.org/10.1002/pmic.201600223</dcterms:isReferencedBy><dcterms:date>2019-05-06</dcterms:date><dcterms:contributor>Konstantinell, Aelita Gloria Virginia</dcterms:contributor><dcterms:dateSubmitted>2019-04-01</dcterms:dateSubmitted><dcterms:temporal>2015-08-01</dcterms:temporal><dcterms:temporal>2015-12-31</dcterms:temporal><dcterms:relation>Biomarkers Discovery: The Benefit of the Study Exosomes Originated from Merkel Cell Carcinoma Cell Lines. doi: 10.18710/KCW912</dcterms:relation><dcterms:type>Experimental data</dcterms:type><dcterms:license>CC0 1.0</dcterms:license></metadata>