<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Adebayo OO</submitter><funding>MSM/TU/UAB</funding><funding>NCRR NIH HHS</funding><funding>MSM</funding><funding>NHLBI NIH HHS</funding><funding>NIMHD NIH HHS</funding><funding>National Cancer Institute</funding><funding>NCI NIH HHS</funding><funding>Ruth L. Kirschstein National Research Service Award</funding><funding>Winship Cancer Institute</funding><pagination>2228</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9104534</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>14(9)</volume><pubmed_abstract>The molecular mechanisms underlying chemoresistance in some newly diagnosed multiple myeloma (MM) patients receiving standard therapies (lenalidomide, bortezomib, and dexamethasone) are poorly understood. Identifying clinically relevant gene networks associated with death due to MM may uncover novel mechanisms, drug targets, and prognostic biomarkers to improve the treatment of the disease. This study used data from the MMRF CoMMpass RNA-seq dataset (N = 270) for weighted gene co-expression network analysis (WGCNA), which identified 21 modules of co-expressed genes. Genes differentially expressed in patients with poor outcomes were assessed using two independent sample &lt;i>t&lt;/i>-tests (dead and alive MM patients). The clinical performance of biomarker candidates was evaluated using overall </pubmed_abstract><journal>Cancers</journal><pubmed_title>Multivariant Transcriptome Analysis Identifies Modules and Hub Genes Associated with Poor Outcomes in Newly Diagnosed Multiple Myeloma Patients.</pubmed_title><pmcid>PMC9104534</pmcid><funding_grant_id>C06 RR018386</funding_grant_id><funding_grant_id>G12MD007602</funding_grant_id><funding_grant_id>1G12RR026250-03</funding_grant_id><funding_grant_id>T32 HL103104</funding_grant_id><funding_grant_id>U54 CA118638</funding_grant_id><funding_grant_id>T32HL103104</funding_grant_id><funding_grant_id>1C06 RR18386</funding_grant_id><funding_grant_id>U54CA118638</funding_grant_id><funding_grant_id>U54MD007602</funding_grant_id><pubmed_authors>Oseni SO</pubmed_authors><pubmed_authors>Jain S</pubmed_authors><pubmed_authors>Barwick BG</pubmed_authors><pubmed_authors>Dill CD</pubmed_authors><pubmed_authors>Adebayo AO</pubmed_authors><pubmed_authors>Ohandjo AQ</pubmed_authors><pubmed_authors>Lillard JW</pubmed_authors><pubmed_authors>Griffen TL</pubmed_authors><pubmed_authors>Adebayo OO</pubmed_authors><pubmed_authors>Dammer EB</pubmed_authors><pubmed_authors>Singh R</pubmed_authors><pubmed_authors>Yan F</pubmed_authors><pubmed_authors>Boise LH</pubmed_authors></additional><is_claimable>false</is_claimable><name>Multivariant Transcriptome Analysis Identifies Modules and Hub Genes Associated with Poor Outcomes in Newly Diagnosed Multiple Myeloma Patients.</name><description>The molecular mechanisms underlying chemoresistance in some newly diagnosed multiple myeloma (MM) patients receiving standard therapies (lenalidomide, bortezomib, and dexamethasone) are poorly understood. Identifying clinically relevant gene networks associated with death due to MM may uncover novel mechanisms, drug targets, and prognostic biomarkers to improve the treatment of the disease. This study used data from the MMRF CoMMpass RNA-seq dataset (N = 270) for weighted gene co-expression network analysis (WGCNA), which identified 21 modules of co-expressed genes. Genes differentially expressed in patients with poor outcomes were assessed using two independent sample &lt;i>t&lt;/i>-tests (dead and alive MM patients). The clinical performance of biomarker candidates was evaluated using overall </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-04-08T09:37:39.379Z</modification><creation>2024-11-07T13:40:26.83Z</creation></dates><accession>S-EPMC9104534</accession><cross_references><pubmed>35565356</pubmed><doi>10.3390/cancers14092228</doi></cross_references></HashMap>