<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/GSE333nnn/GSE333988/</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=GSE333988</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Transcriptomic analysis of GKB202-treated circulating tumor cells isolated from patients with lung cancer and pancreatic cancer</name><description>Circulating tumor cells (CTCs) are associated with metastatic dissemination and adaptive stress responses in cancer. In this study, patient-derived CTCs isolated from lung cancer and pancreatic cancer samples were treated with GKB202, a natural compound derived from Antrodia cinnamomea, to investigate treatment-associated transcriptomic changes. Bulk RNA sequencing was performed to compare untreated/control and GKB202-treated CTC samples. This dataset provides raw sequencing reads and processed gene-level expression matrices for evaluating the effects of GKB202 on CTC-related transcriptional programs, including stress-response and cancer-associated pathways.</description><dates><publication>2026/06/04</publication></dates><accession>GSE333988</accession><cross_references><GSM>GSM9778524</GSM><GSM>GSM9778523</GSM><GSM>GSM9778522</GSM><GSM>GSM9778521</GSM><GSM>GSM9778530</GSM><GSM>GSM9778529</GSM><GSM>GSM9778528</GSM><GSM>GSM9778527</GSM><GSM>GSM9778526</GSM><GSM>GSM9778525</GSM><GPL>18573</GPL><GSE>333988</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>