<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/GSE318nnn/GSE318324/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Transcriptomics</omics_type><species>Homo sapiens</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=GSE318324</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Targeted RNA sequencing of resected hepatocellular carcinoma specimens to characterize immune gene expression associated with spatial PD-L1(+) TAM–CD8(+) T cell interactions</name><description>This study investigates immune-related gene expression profiles associated with spatial interactions between PD-L1-positive tumor-associated macrophages (TAMs) and CD8-positive T cells in hepatocellular carcinoma (HCC). RNA was extracted from tumor regions of formalin-fixed paraffin-embedded (FFPE) specimens obtained from eight patients who underwent hepatectomy. Targeted RNA sequencing was performed using custom AmpliSeq panels covering cancer progression– and immunity-related genes. Raw sequencing data and processed gene expression matrices are provided to enable downstream reanalysis.</description><dates><publication>2026/04/30</publication></dates><accession>GSE318324</accession><cross_references><GSM>GSM9492469</GSM><GSM>GSM9492458</GSM><GSM>GSM9492459</GSM><GSM>GSM9492467</GSM><GSM>GSM9492457</GSM><GSM>GSM9492468</GSM><GSM>GSM9492472</GSM><GSM>GSM9492461</GSM><GSM>GSM9492462</GSM><GSM>GSM9492470</GSM><GSM>GSM9492460</GSM><GSM>GSM9492471</GSM><GSM>GSM9492465</GSM><GSM>GSM9492466</GSM><GSM>GSM9492463</GSM><GSM>GSM9492464</GSM><GPL>15520</GPL><GSE>318324</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>