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Whole Proteome measurement of pancreatic cancer cells (Panc89) or melanoma cells (MaMel47) treated with USP7 inhibitors and degrader to compare phenotypes induced by inhibition compared to degradation. We synthesized and characterized potent USP7-targeting degrader molecules (PROTACs) and compared U...
ORGANISM(S): Homo sapiens (Human) 
2026-04-21 | PXD070431 | Pride
CDK7 inhibition by LDC4297 in Mia-Paca2 and Panc89 cells
Inhibition of the dual function cell cycle and transcription kinase CDK7 is known to affect the viability of cancer cells, but the mechanisms underlying cell line-specific growth control remain poorly understood. Here, we employed a previously developed, highly specific small molecule inhibitor that...
ORGANISM(S): Homo sapiens 
2022-01-21 | GSE193737 | GEO
3' mRNA-seq was used to study the effects of USP7 degradation by the degraders NK266 and NK250 on gene expression in a human melanoma and PDAC cell line, respectively.
ORGANISM(S): Homo sapiens 
Pancreatic ductal adenocarcinoma (PDAC) is the most common malignant pancreatic tumor in western countries, characterized by a low 5-year survival rate of only 11 %. Owing to a lack of early and specific symptoms, most patients are diagnosed at advanced or even me-tastasized stages essentially impai...
ORGANISM(S): Homo sapiens 
2024-08-14 | GSE241182 | GEO
3' mRNA-seq of human Ma-Mel47 (melanoma) and Panc89 (PDAC) cells treated with the USP7 degraders NK250 and NK266, respectively, for 72 h.
Epithelial and mesenchymal pancreatic cancer cells exhibit different stem cell phenotypes being associated with different metastatic propensity
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