<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><submitter>Haas R</submitter><funding>NCI NIH HHS</funding><funding>NIGMS NIH HHS</funding><pubmed_abstract>Multifocal prostate cancer is a prevalent phenomenon, with most cases remaining uncharacterized from a genomic perspective. A patient presented with bilateral prostate cancer. On systematic biopsy, two indistinguishable clinicopathologic lesions were detected. Whole-genome sequencing displayed somatically unrelated tumours with distinct driver CNA regions, suggesting independent origins of the two tumors. We demonstrated that similar clinicopathologic multifocal tumours, which might be interpreted as clonal disease, can in fact represent independent cancers. Genetic prognostics can prevent mischaracterization of multifocal disease to enable optimal patient management.</pubmed_abstract><journal>medRxiv : the preprint server for health sciences</journal><pagination>2024.08.22.24312320</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11370525</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Divergent Evolution in Bilateral Prostate Cancer: a Case Study.</pubmed_title><pmcid>PMC11370525</pmcid><funding_grant_id>R01 CA270108</funding_grant_id><funding_grant_id>T32 GM008042</funding_grant_id><funding_grant_id>P30 CA016042</funding_grant_id><funding_grant_id>U2C CA271894</funding_grant_id><funding_grant_id>P50 CA092131</funding_grant_id><pubmed_authors>Huang RR</pubmed_authors><pubmed_authors>Weiner A</pubmed_authors><pubmed_authors>Liu LY</pubmed_authors><pubmed_authors>Boutros PC</pubmed_authors><pubmed_authors>Patel Y</pubmed_authors><pubmed_authors>Yamaguchi TN</pubmed_authors><pubmed_authors>Haas R</pubmed_authors><pubmed_authors>Reiter RE</pubmed_authors><pubmed_authors>Agrawal R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Divergent Evolution in Bilateral Prostate Cancer: a Case Study.</name><description>Multifocal prostate cancer is a prevalent phenomenon, with most cases remaining uncharacterized from a genomic perspective. A patient presented with bilateral prostate cancer. On systematic biopsy, two indistinguishable clinicopathologic lesions were detected. Whole-genome sequencing displayed somatically unrelated tumours with distinct driver CNA regions, suggesting independent origins of the two tumors. We demonstrated that similar clinicopathologic multifocal tumours, which might be interpreted as clonal disease, can in fact represent independent cancers. Genetic prognostics can prevent mischaracterization of multifocal disease to enable optimal patient management.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Aug</publication><modification>2025-04-18T13:08:32.449Z</modification><creation>2025-04-06T22:39:20.909Z</creation></dates><accession>S-EPMC11370525</accession><cross_references><pubmed>39228741</pubmed><doi>10.1101/2024.08.22.24312320</doi></cross_references></HashMap>