MassIVE MSV000094243

Partial Public

CDKN1B (p27kip1) enhances drug tolerant persister CTCs by restricting polyploidy following mitotic inhibitors

Description

BRx82 and BRx142 were cell cultures derived from breast cancer circulating tumor cells and propagated ex-vivo. To study early changes that transpire under mitosis inhibiting chemotherapy, these cultures were subjected to a 16 hours exposure to docetaxel (10nM or DMSO as vehicle control) and then cultured for a total of 4 days. The experiments were done using an Orbitrap Fusion (proteomics) or an Orbitrap Fusion Lumos (phosphoproteomics) mass spectrometer. Multiplexing was achieved using either TMT10 reagents and the SPS-MS3 method. Basic pH reversed-phase chromatography (bRPLC) was used for off-line pre-fractionation; 12 fractions were analyzed for proteome mappings (PMID: 26700037) and 24 fractions sample for phosphoproteome mappings (PMID: 31606085). Phosphoproteome mappings were done using both HCD fragmentation with Orbitrap fragment ion detection and CID fragmentation with ion trap fragment ion detection (PMID: 29487189, PMID: 31606085). RAW files from the proteome mapping experiment are named HorwitzMaheswaranHaber_proteome_fraction01 to 12. RAW files from the phosphoproteome mapping experiment are named TMT labeling was the same for the proteomics and the phosphoproteomics experiments: BRx82_DTX-_#1 (129c) BRx82_DTX-_#2 (130n) BRx82_DTX+_#1 (127c) BRx82_DTX+_#2 (128n) BRx142_DTX-_#1 (126) BRx142_DTX-_#2 (127n) BRx142_DTX+_#1 (128c) BRx142_DTX+_#2 (129n) [doi:10.25345/C50R9MF75] [dataset license: CC0 1.0 Universal (CC0 1.0)]

Keywords: Breast cancer, circulating tumor cells, chemotherapy, docetaxel, persister cells, proteomics, phosphoproteomics, TMT, TMT10, Orbitrap Fusion, Orbitrap Lumos Fusion, SPS MS3

Contact

Principal Investigators:
(in alphabetical order)
Daniel Haber, Massachusetts General Hospital Cancer Center and Harvard Medical School, US
Shyamala Maheswaran, Massachusetts General Hospital Cancer Center and Harvard Medical School, US
Wilhelm Haas, Massachusetts General Hospital Cancer Center and Harvard Medical School, US
Submitting User: whaas
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