<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>14(12)</volume><submitter>Huang L</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>The mechanisms underlying the pronounced organotropism of breast cancer (BC) for the liver remain incompletely elucidated. This study aims to investigate the role of the tumor microenvironment (TME), particularly tumor-associated neutrophils (TANs), and their metabolic regulation in breast cancer liver metastasis (BCLM).&lt;h4>Methods&lt;/h4>We employed a multi-level integrative approach. Bioinformatic analysis of Gene Expression Omnibus (GEO) datasets characterized the immune landscape of BCLM. Clinical specimens, and &lt;i>in vitro&lt;/i> assays were utilized to define the functional interplay between TANs and BC cells. Metabolomic profiling of patient samples was conducted to characterize metabolic alterations in BCLM.&lt;h4>Results&lt;/h4>A neutrophil-enriched TME was identified as a </pubmed_abstract><journal>Translational cancer research</journal><pagination>8949-8964</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12776239</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Tumor-associated neutrophils drive liver-specific metastatic progression in breast cancer through methionine metabolism mediated by methionine adenosyltransferase II alpha.</pubmed_title><pmcid>PMC12776239</pmcid><pubmed_authors>Ji T</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhen S</pubmed_authors><pubmed_authors>Xu D</pubmed_authors><pubmed_authors>Huang L</pubmed_authors><pubmed_authors>Sun Y</pubmed_authors><pubmed_authors>Chen R</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Zhu Q</pubmed_authors><pubmed_authors>Zha X</pubmed_authors></additional><is_claimable>false</is_claimable><name>Tumor-associated neutrophils drive liver-specific metastatic progression in breast cancer through methionine metabolism mediated by methionine adenosyltransferase II alpha.</name><description>&lt;h4>Background&lt;/h4>The mechanisms underlying the pronounced organotropism of breast cancer (BC) for the liver remain incompletely elucidated. This study aims to investigate the role of the tumor microenvironment (TME), particularly tumor-associated neutrophils (TANs), and their metabolic regulation in breast cancer liver metastasis (BCLM).&lt;h4>Methods&lt;/h4>We employed a multi-level integrative approach. Bioinformatic analysis of Gene Expression Omnibus (GEO) datasets characterized the immune landscape of BCLM. Clinical specimens, and &lt;i>in vitro&lt;/i> assays were utilized to define the functional interplay between TANs and BC cells. Metabolomic profiling of patient samples was conducted to characterize metabolic alterations in BCLM.&lt;h4>Results&lt;/h4>A neutrophil-enriched TME was identified as a </description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Dec</publication><modification>2026-07-15T06:08:36.54Z</modification><creation>2026-06-30T03:21:22.727Z</creation></dates><accession>S-EPMC12776239</accession><cross_references><pubmed>41510096</pubmed><doi>10.21037/tcr-2025-aw-2278</doi></cross_references></HashMap>