<?xml version='1.0' encoding='UTF-8'?><codeBook xmlns="ddi:codebook:2_5" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="ddi:codebook:2_5 https://ddialliance.org/Specification/DDI-Codebook/2.5/XMLSchema/codebook.xsd" version="2.5"><docDscr><citation><titlStmt><titl>Replication Data for: Secretomic analysis of extracellular vesicles originating from polyomavirus-negative and polyomavirus-positive Merkel cell carcinoma cell lines</titl><IDNo agency="DOI">doi:10.18710/USXCRS</IDNo></titlStmt><distStmt><distrbtr source="archive">DataverseNO</distrbtr><distDate>2019-05-06</distDate></distStmt><verStmt source="archive"><version date="2019-05-13" type="RELEASED">1</version></verStmt><biblCit>Konstantinell, Aelita Gloria Virginia, 2019, "Replication Data for: Secretomic analysis of extracellular vesicles originating from polyomavirus-negative and polyomavirus-positive Merkel cell carcinoma cell lines", https://doi.org/10.18710/USXCRS, DataverseNO, V1, UNF:6:xGarNwkr+cO6GOAu/OngFQ== [fileUNF]</biblCit></citation></docDscr><stdyDscr><citation><titlStmt><titl>Replication Data for: Secretomic analysis of extracellular vesicles originating from polyomavirus-negative and polyomavirus-positive Merkel cell carcinoma cell lines</titl><IDNo agency="DOI">doi:10.18710/USXCRS</IDNo></titlStmt><rspStmt><AuthEnty affiliation="UiT The Arctic University of Norway">Konstantinell, Aelita Gloria Virginia</AuthEnty></rspStmt><prodStmt><producer abbr="UiT">UiT The Arctic University of Norway</producer><grantNo agency="Odd Fellow Medisinsk-Vitenskapelig Forskningsfond">2A65216</grantNo></prodStmt><distStmt><distrbtr source="archive">DataverseNO</distrbtr><distrbtr affiliation="UiT The Arctic University of Norway" URI="https://dataverse.no/dataverse/uit">UiT The Arctic University of Norway</distrbtr><contact affiliation="UiT The Arctic University of Norway" email="aelita.g.konstantinell@uit.no">Konstantinell, Aelita Gloria Virginia</contact><depositr>Konstantinell, Aelita Gloria Virginia</depositr><depDate>2019-04-01</depDate></distStmt><holdings URI="https://doi.org/10.18710/USXCRS"/></citation><stdyInfo><subject><keyword xml:lang="en">Medicine, Health and Life Sciences</keyword><keyword>Merkel cell carcinoma</keyword><keyword>Merkel cell polyomavirus</keyword><keyword>Exosome</keyword><keyword>Proteomics</keyword></subject><abstract date="2019-04-01">This dataset is about analyses of two Merkel cell polyomavirus (MCPyV)-negative and two MCPyV–positive Merkel cell lines secretomic proteins.</abstract><abstract date="2019-04-01">&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.</abstract><sumDscr><collDate cycle="P1" event="start" date="2015-08-01">2015-08-01</collDate><collDate cycle="P1" event="end" date="2015-12-31">2015-12-31</collDate><dataKind>Experimental data</dataKind></sumDscr></stdyInfo><method><dataColl><sources/></dataColl><anlyInfo/></method><dataAccs><setAvail/><useStmt/><notes type="DVN:TOU" level="dv">&lt;a href="http://creativecommons.org/publicdomain/zero/1.0">CC0 1.0&lt;/a></notes></dataAccs><othrStdyMat><relStdy>Biomarkers Discovery: The Benefit of the Study Exosomes Originated from Merkel Cell Carcinoma Cell Lines. doi: 10.18710/KCW912</relStdy><relPubl><citation><titlStmt><titl>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.</titl><IDNo agency="doi">10.1002/pmic.201600223</IDNo></titlStmt><biblCit>A. Konstantinell, et al. Secretomic analysis of extracellular vesicles originating from polyomavirus-negative and polyomavirus-positive Merkel cell carcinoma cell lines. 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