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Coordinating catalytic and non-canonical functions of EZH2 sensitizes tumors to CAR-T cell therapy

GSE323364 Homo sapiens Genome binding/occupancy profiling by high throughput sequencing; Expression profiling by high throughput sequencing 42 samples Submitted 2026/05/21 Platform GPL20301
Summary
This study investigates the dual roles of EZH2 (catalytic and non-canonical) in regulating tumor cell adhesion and sensitivity to CAR-T cell therapy. We performed RNA-seq and CUT&Tag-seq (anti-EZH2) on three human triple-negative breast cancer cell lines (MDA-MB-436, MDA-MB-468, HCC1806) treated with the EZH2 inhibitor EPZ-6438. Additionally, RNA-seq was performed on MDA-MB-468 cells with EZH2 knockdown to dissect the EZH2-dependent transcriptomic underlying tumor cell adhesion and CAR-T therapy response.
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Direct links to NCBI, no account and no request form: the whole study as GSE323364_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 PRJNA1432532 and SRA study SRP681163. Searching any of these in the dataset finder brings you back here.

Study design
14 conditions, mostly in triplicate
RNA-seq of MDA-MB-468 EPZ-6438 ×3 RNA-seq of MDA-MB-468 DMSO ×3 CUT&Tag of MDA-MB-468 EPZ-6438 ×3 CUT&Tag of MDA-MB-468 DMSO ×3 RNA-seq of MDA-MB-436 EPZ-6438 ×3 RNA-seq of MDA-MB-436 DMSO ×3 CUT&Tag of MDA-MB-436 EPZ-6438 ×3 CUT&Tag of MDA-MB-436 DMSO ×3 +6 more

Supports a between-group comparison across 40 samples.

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