Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.




Homo sapiens


Part of: Cancer Cell Line Encyclopedia (CCLE) project. Part of: COSMIC cell lines project. Microsatellite instability: Stable (MSS) (Sanger). Omics: Array-based CGH. Omics: Deep exome analysis. Omics: Deep RNAseq analysis. Omics: DNA methylation analysis. Omics: SNP array analysis. Omics: Transcriptome analysis. Genome ancestry: African=0.75%; Native American=0%; East Asian, North=0.77%; East Asian, South=0.91%; South Asian=0%; European, North=67.35%; European, South=30.22% (PubMed=30894373). DT Created: 06-06-12; Last updated: 06-09-19; Version: 22

Proper Citation



Cancer cell line DT Created: 06-06-12; Last updated: 06-09-19; Version: 22


DT Created: 06-06-12; Last updated: 06-09-19; Version: 22


H2369, H-2369 DT Created: 06-06-12, Last updated: 06-09-19, Version: 22

Cross References

EFO; EFO_0006678 ArrayExpress; E-MTAB-2706 ArrayExpress; E-MTAB-3610 BioSample; SAMN03471012 CCLE; H2369_PLEURA Cell_Model_Passport; SIDM00104 Cosmic; 1995411 Cosmic-CLP; 1290808 DepMap; ACH-002123 GDSC; 1290808 GEO; GSM1669818 PharmacoDB; NCIH2369_1088_2019 Wikidata; Q54907968 DT Created: 06-06-12; Last updated: 06-09-19; Version: 22


DT Created: 06-06-12; Last updated: 06-09-19; Version: 22

Originate from Same Individual

DT Created: 06-06-12; Last updated: 06-09-19; Version: 22

Publications that use this research resource

Loss of functional BAP1 augments sensitivity to TRAIL in cancer cells.

  • Kolluri KK
  • Elife
  • 2018 Jan 18

Literature context:


Malignant mesothelioma (MM) is poorly responsive to systemic cytotoxic chemotherapy and invariably fatal. Here we describe a screen of 94 drugs in 15 exome-sequenced MM lines and the discovery of a subset defined by loss of function of the nuclear deubiquitinase BRCA associated protein-1 (BAP1) that demonstrate heightened sensitivity to TRAIL (tumour necrosis factor-related apoptosis-inducing ligand). This association is observed across human early passage MM cultures, mouse xenografts and human tumour explants. We demonstrate that BAP1 deubiquitinase activity and its association with ASXL1 to form the Polycomb repressive deubiquitinase complex (PR-DUB) impacts TRAIL sensitivity implicating transcriptional modulation as an underlying mechanism. Death receptor agonists are well-tolerated anti-cancer agents demonstrating limited therapeutic benefit in trials without a targeting biomarker. We identify BAP1 loss-of-function mutations, which are frequent in MM, as a potential genomic stratification tool for TRAIL sensitivity with immediate and actionable therapeutic implications.

Funding information:
  • Cancer Research UK - A17341()
  • NINDS NIH HHS - R01NS043915(United States)
  • Wellcome - WT097452MA()
  • Wellcome Trust - 106555/Z/14/Z()
  • Wellcome Trust - WT107963AIA()