<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kozminsky M</submitter><funding>U.S. Department of Defense</funding><funding>A. Alfred Taubman Medical Research Institute</funding><funding>NCI NIH HHS</funding><funding>National Institutes of Health</funding><funding>Prostate Cancer Foundation</funding><funding>NIH HHS</funding><funding>National Science Foundation</funding><pagination>1801254</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6343066</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(2)</volume><pubmed_abstract>Rates of progression and treatment response in advanced prostate cancer are highly variable, necessitating non-invasive methods to assess the molecular characteristics of these tumors in real time. The unique potential of circulating tumor cells (CTCs) to serve as a clinically useful liquid biomarker is due to their ability to inform via both enumeration and RNA expression. A microfluidic graphene oxide-based device (GO Chip) is used to isolate CTCs and CTC clusters from the whole blood of 41 men with metastatic castration-resistant prostate cancer. Additionally, the expression of 96 genes of interest is determined by RT-qPCR. Multivariate analyses are conducted to determine the genes most closely associated with overall survival, PSA progression, and radioclinical progression. A prelimina</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Detection of CTC Clusters and a Dedifferentiated RNA-Expression Survival Signature in Prostate Cancer.</pubmed_title><pmcid>PMC6343066</pmcid><funding_grant_id>1DP2OD006672‐01</funding_grant_id><funding_grant_id>DGE 1256260</funding_grant_id><funding_grant_id>DP2 OD006672</funding_grant_id><funding_grant_id>W81XWH‐14‐1‐0287</funding_grant_id><funding_grant_id>R33 CA202867</funding_grant_id><funding_grant_id>R01 CA208335</funding_grant_id><pubmed_authors>Azizi E</pubmed_authors><pubmed_authors>Fouladdel S</pubmed_authors><pubmed_authors>Smith DC</pubmed_authors><pubmed_authors>Alva A</pubmed_authors><pubmed_authors>Morgan T</pubmed_authors><pubmed_authors>Nagrath S</pubmed_authors><pubmed_authors>Chung JS</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Kozminsky M</pubmed_authors></additional><is_claimable>false</is_claimable><name>Detection of CTC Clusters and a Dedifferentiated RNA-Expression Survival Signature in Prostate Cancer.</name><description>Rates of progression and treatment response in advanced prostate cancer are highly variable, necessitating non-invasive methods to assess the molecular characteristics of these tumors in real time. The unique potential of circulating tumor cells (CTCs) to serve as a clinically useful liquid biomarker is due to their ability to inform via both enumeration and RNA expression. A microfluidic graphene oxide-based device (GO Chip) is used to isolate CTCs and CTC clusters from the whole blood of 41 men with metastatic castration-resistant prostate cancer. Additionally, the expression of 96 genes of interest is determined by RT-qPCR. Multivariate analyses are conducted to determine the genes most closely associated with overall survival, PSA progression, and radioclinical progression. A prelimina</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Jan</publication><modification>2025-04-04T19:07:34.248Z</modification><creation>2019-03-26T22:43:46Z</creation></dates><accession>S-EPMC6343066</accession><cross_references><pubmed>30693182</pubmed><doi>10.1002/advs.201801254</doi></cross_references></HashMap>