<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE327nnn/GSE327454/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Mus musculus</species><gds_type>Expression profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE327454</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>TET2-mutant clonal hematopoiesis prevents T-cell exhaustion and suppresses cancer metastasis [RNA-seq]</name><description>TET2-mutant clonal hematopoiesis (CH) is associated with reduced cancer metastasis in human cohorts. Using mouse models of colorectal cancer liver metastasis, we demonstrate that Tet2-deficient hematopoietic cells suppress metastatic tumor burden by preventing CD8+ T-cell exhaustion. Bulk RNA-seq of sorted CD4+ and CD8+ tumor-infiltrating lymphocytes (TILs) from Vav1CreTet2KO, Cd4CreTet2KO, and Tet2fl/fl control mice was performed to characterize transcriptional changes associated with Tet2 loss in tumor-infiltrating T cells.</description><dates><publication>2026/04/17</publication></dates><accession>GSE327454</accession><cross_references><GSM>GSM9657556</GSM><GSM>GSM9657545</GSM><GSM>GSM9657557</GSM><GSM>GSM9657546</GSM><GSM>GSM9657543</GSM><GSM>GSM9657554</GSM><GSM>GSM9657555</GSM><GSM>GSM9657544</GSM><GSM>GSM9657552</GSM><GSM>GSM9657553</GSM><GSM>GSM9657542</GSM><GSM>GSM9657550</GSM><GSM>GSM9657551</GSM><GSM>GSM9657549</GSM><GSM>GSM9657558</GSM><GSM>GSM9657547</GSM><GSM>GSM9657559</GSM><GSM>GSM9657548</GSM><GSM>GSM9657560</GSM><GPL>21273</GPL><GSE>327454</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>