<HashMap><database>GEO</database><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=GSE292485</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Cancer stem cells are hyper-responsive sensors of tumor microenvironment in orchestrating metastasis dynamics</name><description>Cancer stem cells (CSCs) are key drivers of metastasis and therapy resistance but have been challenging to visualize and study in situ. Using a fluorescent CSC reporter, we observed very different population dynamics for CSCs and nonCSCs during metastatic lung colonization in breast cancer models. CSC expansive self-renewal drives early lesion formation before switching to a maintenance mode of balanced self-renewal and differentiation, whereupon nonCSC proliferation takes over as the main driver of metastatic expansion. Mechanistic analyses showed that CSCs are hyper-responsive to microenvironmental cues such as cell crowding and nutrient availability, suggesting a novel role for CSCs as sensors and early responders to fluctuating local conditions in the tumor. Most inputs converge on YAP/TAZ/TEAD, with heightened CSC sensitivity and response supported by elevated receptor expression and increased chromatin accessibility around enhancers with TEAD binding sites. Targeting inputs to the YAP/TAZ/TEAD node reversed chemotherapy-induced enrichment of CSCs in lung metastases.</description><dates><publication>2026/05/11</publication></dates><accession>GSE292485</accession><cross_references><GSM>GSM8859906</GSM><GSM>GSM8859907</GSM><GSM>GSM8859904</GSM><GSM>GSM8859905</GSM><GSM>GSM8859902</GSM><GSM>GSM8859903</GSM><GSM>GSM8859900</GSM><GSM>GSM8859901</GSM><GPL>16791</GPL><GSE>292485</GSE><taxon>Homo sapiens</taxon></cross_references></HashMap>