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Epigenetic reprogramming drives cellular and phenotypic plasticity in liposarcoma

GSE324208 Homo sapiens Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing 42 samples Submitted 2026/04/01 Platform GPL24676
Summary
Single-cell multiomic profiling were performed to characterize the cellular and regulatory heterogeneity of liposarcoma (LPS), including well-differentiated liposarcoma (WDLPS) and de-differentiated liposarcoma (DDLPS), which exhibit markedly different clinical behaviors. Integrated scRNA and scATAC were used to resolve tumor cell states, gene regulatory programs, and tumor microenvironment composition across LPS subtypes. The results reveal distinct differentiation landscapes, with DDLPS enriched for progenitor-like mesenchymal cells, sclerotic WDLPS displaying broader lineage plasticity, and adipocytic WDLPS dominated by terminally differentiated adipocytes. Analysis of the tumor microenvironment further demonstrates differences in immune composition, with DDLPS enriched for immunosuppressive macrophages. Sclerotic WDLPS exhibits intermediate cellular and molecular features between the two subtypes. Together, these datasets provide a comprehensive resource describing the transcriptional, epigenomic, and microenvironmental diversity of liposarcoma.
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Direct links to NCBI, no account and no request form: the whole study as GSE324208_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 42 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1367140. Searching any of these in the dataset finder brings you back here.

Study design
40 conditions, each sampled once — no replicated groups

Read from the first 40 of 42 sample titles: 40 distinct titles with little repetition. Check it against the sample list below before relying on it.

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