<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>9(1)</volume><submitter>Cai Y</submitter><pubmed_abstract>Polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) are crucial mediators of tumor-induced immunosuppression, while their heterogeneity and spatial dynamics across malignancies remain poorly understood. By integrating single-cell RNA sequencing data from 576 samples across 19 cancer types and spatial transcriptomics data from three distinct malignancies, we identified a PMN-MDSC population. This cell population demonstrated characteristic upregulation of immunosuppressive genes and was associated with poor prognosis across multiple cancer cohorts. Notably, TREM1 was highly expressed in PMN-MDSCs and may mediate immunosuppressive processes. Multiplex immunofluorescence demonstrated that TREM1&lt;sup>+&lt;/sup> PMN-MDSCs exhibited significantly higher distribution in tumor regions compa</pubmed_abstract><journal>Communications biology</journal><pagination>75</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12820143</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Pan-cancer analysis reveals TREM1&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; PMN-MDSCs as critical regulators of immune suppression and tumor microenvironment remodeling.</pubmed_title><pmcid>PMC12820143</pmcid><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Zheng X</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Yang M</pubmed_authors><pubmed_authors>Teng H</pubmed_authors><pubmed_authors>Tang H</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Zou Z</pubmed_authors><pubmed_authors>Wang P</pubmed_authors><pubmed_authors>Li S</pubmed_authors><pubmed_authors>Luo K</pubmed_authors><pubmed_authors>Huang X</pubmed_authors><pubmed_authors>Cai Y</pubmed_authors><pubmed_authors>Feng W</pubmed_authors><pubmed_authors>Liao S</pubmed_authors><pubmed_authors>Wu W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pan-cancer analysis reveals TREM1&amp;lt;sup&amp;gt;+&amp;lt;/sup&amp;gt; PMN-MDSCs as critical regulators of immune suppression and tumor microenvironment remodeling.</name><description>Polymorphonuclear myeloid-derived suppressor cells (PMN-MDSCs) are crucial mediators of tumor-induced immunosuppression, while their heterogeneity and spatial dynamics across malignancies remain poorly understood. By integrating single-cell RNA sequencing data from 576 samples across 19 cancer types and spatial transcriptomics data from three distinct malignancies, we identified a PMN-MDSC population. This cell population demonstrated characteristic upregulation of immunosuppressive genes and was associated with poor prognosis across multiple cancer cohorts. Notably, TREM1 was highly expressed in PMN-MDSCs and may mediate immunosuppressive processes. Multiplex immunofluorescence demonstrated that TREM1&lt;sup>+&lt;/sup> PMN-MDSCs exhibited significantly higher distribution in tumor regions compa</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-06-06T18:13:13.236Z</modification><creation>2026-06-04T03:12:12.776Z</creation></dates><accession>S-EPMC12820143</accession><cross_references><pubmed>41413734</pubmed><doi>10.1038/s42003-025-09342-8</doi></cross_references></HashMap>