<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Mapelli, Sarah N.</dc:creator>
  <dc:creator>Albino, Domenico</dc:creator>
  <dc:creator>Mello-Grand, Maurizia</dc:creator>
  <dc:creator>Shinde, Dheeraj</dc:creator>
  <dc:creator>Scimeca, Manuel</dc:creator>
  <dc:creator>Bonfiglio, Rita</dc:creator>
  <dc:creator>Bonanno, Elena</dc:creator>
  <dc:creator>Chiorino, Giovanna</dc:creator>
  <dc:creator>Garcia-Escudero, Ramon</dc:creator>
  <dc:creator>Catapano, Carlo V.</dc:creator>
  <dc:creator>Carbone, Giuseppina M.</dc:creator>
  <dc:date>2020-01-10</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">In this study, we extracted prostate cell-specific gene sets (metagenes) to define the epithelial differentiation status of  prostate cancers and, using a deconvolution-based strategy, interrogated thousands of primary and metastatic tumors in  public gene profiling datasets. We identified a subgroup of primary prostate tumors with low luminal epithelial enrichment  (LumElow). LumElow tumors were associated with higher Gleason score and mutational burden, reduced relapse-free  and overall survival, and were more likely to progress to castration-resistant prostate cancer (CRPC). Using discriminant  function analysis, we generate a predictive 10-gene classifier for clinical implementation. This mini-classifier predicted  with high accuracy the luminal status in both primary tumors and CRPCs. Immunohistochemistry for COL4A1, a low- luminal marker, sustained the association of attenuated luminal phenotype with metastatic disease. We found also an  association of LumE score with tumor phenotype in genetically engineered mouse models (GEMMs) of prostate cancer.  Notably, the metagene approach led to the discovery of drugs that could revert the low luminal status in prostate cell  lines and mouse models. This study describes a novel tool to dissect the intrinsic heterogeneity of prostate tumors and  provide predictive information on clinical outcome and treatment response in experimental and clinical samples.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://susi.usi.ch/global/documents/318921</dc:identifier>
  <dc:identifier>https://n2t.net/ark:/12658/srd1318921</dc:identifier>
  <dc:identifier>https://susi.usi.ch/documents/318921/files/Mapelli_cancers_2020.pdf</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.3390/cancers12010176</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/ark/12658/srd1318921</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>CC BY</dc:rights>
  <dc:source>Cancers. - 2020, vol. 12, no. 1, p. 23 p</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Prostate cancer</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Tumor classification</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Predictive biomarkers</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Gene signature</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Gene classifier</dc:subject>
  <dc:subject>info:eu-repo/classification/udc/61</dc:subject>
  <dc:title xmlns:ns6="xml" ns6:lang="en">A novel prostate cell type-specific gene signature to interrogate prostate tumor differentiation status and monitor therapeutic response (running title: Phenotypic classification of prostate tumors)</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
