<?xml version="1.0" encoding="UTF-8"?>
<resource xmlns="http://datacite.org/schema/kernel-4" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://datacite.org/schema/kernel-4 http://schema.datacite.org/meta/kernel-4.5/metadata.xsd">
  <identifier identifierType="DOI">10.18710/USXCRS</identifier>
  <creators>
    <creator>
      <creatorName nameType="Personal">Konstantinell, Aelita Gloria Virginia</creatorName>
      <givenName>Aelita Gloria Virginia</givenName>
      <familyName>Konstantinell</familyName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
    </creator>
  </creators>
  <titles>
    <title>Replication Data for: Secretomic analysis of extracellular vesicles originating from polyomavirus-negative and polyomavirus-positive Merkel cell carcinoma cell lines</title>
  </titles>
  <publisher>DataverseNO</publisher>
  <publicationYear>2019</publicationYear>
  <subjects>
    <subject>Medicine, Health and Life Sciences</subject>
    <subject>Merkel cell carcinoma</subject>
    <subject>Merkel cell polyomavirus</subject>
    <subject>Exosome</subject>
    <subject>Proteomics</subject>
  </subjects>
  <contributors>
    <contributor contributorType="Producer">
      <contributorName nameType="Organizational">UiT The Arctic University of Norway</contributorName>
    </contributor>
    <contributor contributorType="Distributor">
      <contributorName nameType="Organizational">UiT The Arctic University of Norway</contributorName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
    </contributor>
    <contributor contributorType="ContactPerson">
      <contributorName nameType="Personal">Konstantinell, Aelita Gloria Virginia</contributorName>
      <givenName>Aelita Gloria Virginia</givenName>
      <familyName>Konstantinell</familyName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
    </contributor>
  </contributors>
  <dates>
    <date dateType="Submitted">2019-04-01</date>
    <date dateType="Available">2019-05-06</date>
    <date dateType="Updated">2019-05-13</date>
    <date dateType="Collected">2015-08-01/2015-12-31</date>
  </dates>
  <resourceType resourceTypeGeneral="Dataset">Experimental data</resourceType>
  <relatedIdentifiers>
    <relatedIdentifier relationType="IsSupplementTo" relatedIdentifierType="DOI">10.1002/PMIC.201600223</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/GYUFPQ</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/IRUGPH</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/GRUGKV</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/R7F8QG</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/HAIGG2</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/YGAJUZ</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/9JBLDY</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/4KVUUX</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/JRVCQY</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/IKNWIB</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/VI3SJW</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/MCWNRV</relatedIdentifier>
    <relatedIdentifier relationType="HasPart" relatedIdentifierType="DOI">10.18710/USXCRS/MZCHPQ</relatedIdentifier>
  </relatedIdentifiers>
  <sizes>
    <size>3738</size>
    <size>77048</size>
    <size>386890</size>
    <size>26579</size>
    <size>65017</size>
    <size>4001</size>
    <size>11602</size>
    <size>1770</size>
    <size>330002</size>
    <size>10573</size>
    <size>16908</size>
    <size>3964</size>
    <size>13528</size>
  </sizes>
  <formats>
    <format>text/plain</format>
    <format>text/plain</format>
    <format>text/plain</format>
    <format>application/vnd.openxmlformats-officedocument.spreadsheetml.sheet</format>
    <format>application/vnd.openxmlformats-officedocument.spreadsheetml.sheet</format>
    <format>text/tab-separated-values</format>
    <format>application/vnd.openxmlformats-officedocument.spreadsheetml.sheet</format>
    <format>text/plain</format>
    <format>application/vnd.openxmlformats-officedocument.spreadsheetml.sheet</format>
    <format>application/vnd.openxmlformats-officedocument.spreadsheetml.sheet</format>
    <format>text/plain</format>
    <format>text/plain</format>
    <format>text/plain</format>
  </formats>
  <version>1.1</version>
  <rightsList>
    <rights rightsURI="info:eu-repo/semantics/openAccess"/>
    <rights rightsURI="http://creativecommons.org/publicdomain/zero/1.0" rightsIdentifier="CC0-1.0" rightsIdentifierScheme="SPDX" schemeURI="https://spdx.org/licenses/" xml:lang="en">Creative Commons CC0 1.0 Universal Public Domain Dedication.</rights>
  </rightsList>
  <descriptions>
    <description descriptionType="Abstract">This dataset is about analyses of two Merkel cell polyomavirus (MCPyV)-negative and two MCPyV–positive Merkel cell lines secretomic proteins.</description>
    <description descriptionType="Abstract">&amp;lt;/p&amp;gt;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&#13;
in pathologies, including malignancy, their importance as prognostic and diagnostic markers,&#13;
and their potential as a therapeutic tool. Merkel cell carcinoma (MCC) is an aggressive form of&#13;
skin cancer with a poor prognosis. Because an effective systemic treatment for this cancer type&#13;
is currently not available, an exosome-based therapy was proposed. However, comprehensive&#13;
secretome profiling has not been performed for MCC. To help unveil the putative contribution&#13;
of exosomes in MCC, we studied the protein content of MCC-derived exosomes. Since approximately&#13;
80% of all MCC cases contain Merkel cell polyomavirus (MCPyV), the secretomes of&#13;
two MCPyV-negative and two MCPyV-positive MCC cell lines were compared. We identified&#13;
with high confidence 164 exosome-derived proteins common for all four cell lines that were annotated&#13;
in ExoCarta and Vesiclepedia databases. These include proteins implicated in motility,&#13;
metastasis and tumor progression, such as integrins and tetraspanins, intracellular signaling&#13;
molecules, chaperones, proteasomal proteins, and translation factors. Additional virus-negative&#13;
and virus-positiveMCC cell lines should be examined to identify highly representative exosomal&#13;
proteins that may provide reliable prognostic and diagnostic biomarkers, as well as targets for&#13;
treatment in the future. Data are available via ProteomeXchange with identifier PXD004198.</description>
  </descriptions>
  <fundingReferences>
    <fundingReference>
      <funderName>Odd Fellow Medisinsk-Vitenskapelig Forskningsfond</funderName>
      <awardNumber>2A65216</awardNumber>
    </fundingReference>
  </fundingReferences>
</resource>
