<HashMap><database>ENA</database><scores/><additional><omics_type>Genomics</omics_type><center_name>NCI</center_name><full_dataset_link>https://www.ebi.ac.uk/ena/browser/view/PRJNA1194672</full_dataset_link><scientific_name>Homo sapiens</scientific_name><long_description>Mantle cell lymphoma (MCL) is a genetically and clinically heterogeneous B-cell malignancy. We studied two MCL cohorts with differing treatment patterns: one enriched for immunochemotherapy, the other for chemotherapy alone. TP53 alterations are consistently associated with poor prognosis, whereas ATM mutations correlate with improved outcomes following rituximab-based chemotherapy. Based on recurrent genetic events, six clusters are identified and refined into three prognostic groups: high-risk (TP53 mutations and deletions at 17p13.3, 13q14.2, and 19p13.3), intermediate-risk (ATM and epigenetic regulator mutations, or gains at 8q/17q/15q), and low-risk (lacking TP53 alterations, rare ATM mutations without 11q deletions, gains at 3q, deletions at 6q). Transcriptomic analysis reveals... (for more see dbGaP study page.)</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>Functional Genomics and Tumor Microenvironment Analysis Reveal Prognostic Biological Subtypes in Mantle Cell Lymphoma</name><description>Functional Genomics and Tumor Microenvironment Analysis Reveal Prognostic Biological Subtypes in Mantle Cell Lymphoma</description><dates><last_updated>2025-09-24</last_updated><first_public>2025-04-29</first_public></dates><accession>PRJNA1194672</accession><cross_references><taxon>9606</taxon></cross_references></HashMap>