<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Chen D</submitter><funding>Shanghai Shenkang Hospital Development Center</funding><funding>National Natural Science Foundation of China</funding><funding>Special Funds for the Basic Research and Development Program in the Central Non-profit Research Institutesof China</funding><pagination>125</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11044366</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>43(1)</volume><pubmed_abstract>&lt;h4>Background&lt;/h4>Immunotherapy has emerged as a potent clinical approach for cancer treatment, but only subsets of cancer patients can benefit from it. Targeting lactate metabolism (LM) in tumor cells as a method to potentiate anti-tumor immune responses represents a promising therapeutic strategy.&lt;h4>Methods&lt;/h4>Public single-cell RNA-Seq (scRNA-seq) cohorts collected from patients who received immunotherapy were systematically gathered and scrutinized to delineate the association between LM and the immunotherapy response. A novel LM-related signature (LM.SIG) was formulated through an extensive examination of 40 pan-cancer scRNA-seq cohorts. Then, multiple machine learning (ML) algorithms were employed to validate the capacity of LM.SIG for immunotherapy response prediction and surviva</pubmed_abstract><journal>Journal of experimental &amp; clinical cancer research : CR</journal><pubmed_title>Pan-cancer analysis implicates novel insights of lactate metabolism into immunotherapy response prediction and survival prognostication.</pubmed_title><pmcid>PMC11044366</pmcid><funding_grant_id>SHDC2020CR5008</funding_grant_id><funding_grant_id>82073326</funding_grant_id><funding_grant_id>202303021212363</funding_grant_id><funding_grant_id>82273356</funding_grant_id><pubmed_authors>Li H</pubmed_authors><pubmed_authors>Li J</pubmed_authors><pubmed_authors>Lu X</pubmed_authors><pubmed_authors>Liu P</pubmed_authors><pubmed_authors>Shen B</pubmed_authors><pubmed_authors>Chen D</pubmed_authors><pubmed_authors>Liu Y</pubmed_authors><pubmed_authors>Zang L</pubmed_authors><pubmed_authors>Zhai S</pubmed_authors><pubmed_authors>Fu D</pubmed_authors><pubmed_authors>Weng Y</pubmed_authors><pubmed_authors>Qi D</pubmed_authors><pubmed_authors>Lin J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Pan-cancer analysis implicates novel insights of lactate metabolism into immunotherapy response prediction and survival prognostication.</name><description>&lt;h4>Background&lt;/h4>Immunotherapy has emerged as a potent clinical approach for cancer treatment, but only subsets of cancer patients can benefit from it. Targeting lactate metabolism (LM) in tumor cells as a method to potentiate anti-tumor immune responses represents a promising therapeutic strategy.&lt;h4>Methods&lt;/h4>Public single-cell RNA-Seq (scRNA-seq) cohorts collected from patients who received immunotherapy were systematically gathered and scrutinized to delineate the association between LM and the immunotherapy response. A novel LM-related signature (LM.SIG) was formulated through an extensive examination of 40 pan-cancer scRNA-seq cohorts. Then, multiple machine learning (ML) algorithms were employed to validate the capacity of LM.SIG for immunotherapy response prediction and surviva</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Apr</publication><modification>2026-06-01T11:18:51.36Z</modification><creation>2026-04-08T11:47:43.518Z</creation></dates><accession>S-EPMC11044366</accession><cross_references><pubmed>38664705</pubmed><doi>10.1186/s13046-024-03042-7</doi></cross_references></HashMap>