Pular para o conteúdo
Merck

Proteogenomic Landscape of Breast Cancer Tumorigenesis and Targeted Therapy.

Cell (2020-11-20)
Karsten Krug, Eric J Jaehnig, Shankha Satpathy, Lili Blumenberg, Alla Karpova, Meenakshi Anurag, George Miles, Philipp Mertins, Yifat Geffen, Lauren C Tang, David I Heiman, Song Cao, Yosef E Maruvka, Jonathan T Lei, Chen Huang, Ramani B Kothadia, Antonio Colaprico, Chet Birger, Jarey Wang, Yongchao Dou, Bo Wen, Zhiao Shi, Yuxing Liao, Maciej Wiznerowicz, Matthew A Wyczalkowski, Xi Steven Chen, Jacob J Kennedy, Amanda G Paulovich, Mathangi Thiagarajan, Christopher R Kinsinger, Tara Hiltke, Emily S Boja, Mehdi Mesri, Ana I Robles, Henry Rodriguez, Thomas F Westbrook, Li Ding, Gad Getz, Karl R Clauser, David Fenyö, Kelly V Ruggles, Bing Zhang, D R Mani, Steven A Carr, Matthew J Ellis, Michael A Gillette
RESUMO

The integration of mass spectrometry-based proteomics with next-generation DNA and RNA sequencing profiles tumors more comprehensively. Here this "proteogenomics" approach was applied to 122 treatment-naive primary breast cancers accrued to preserve post-translational modifications, including protein phosphorylation and acetylation. Proteogenomics challenged standard breast cancer diagnoses, provided detailed analysis of the ERBB2 amplicon, defined tumor subsets that could benefit from immune checkpoint therapy, and allowed more accurate assessment of Rb status for prediction of CDK4/6 inhibitor responsiveness. Phosphoproteomics profiles uncovered novel associations between tumor suppressor loss and targetable kinases. Acetylproteome analysis highlighted acetylation on key nuclear proteins involved in the DNA damage response and revealed cross-talk between cytoplasmic and mitochondrial acetylation and metabolism. Our results underscore the potential of proteogenomics for clinical investigation of breast cancer through more accurate annotation of targetable pathways and biological features of this remarkably heterogeneous malignancy.

MATERIAIS
Número do produto
Marca
Descrição do produto

Sigma-Aldrich
Ácido trifluoracético, suitable for HPLC, ≥99.0%
Sigma-Aldrich
Fosfato de potássio, ACS reagent, ≥99.0%
Sigma-Aldrich
Fosfato de sódio, ACS reagent, ≥99.0%
Sigma-Aldrich
Fosfato de potássio, ACS reagent, ≥98%
Sigma-Aldrich
Ácido fórmico, reagent grade, ≥95%
Sigma-Aldrich
Hidróxido de amônio, 28% NH3 in H2O, ≥99.99% trace metals basis
Sigma-Aldrich
Coquetel inibidor de fosfatase 2, aqueous solution (dark coloration may develop upon storage, which does not affect the activity)
Sigma-Aldrich
Coquetel inibidor de fosfatase 3, DMSO solution
Sigma-Aldrich
Iodoacetamida, Single use vial of 56 mg
Sigma-Aldrich
Hydroxylamine solution, 50 wt. % in H2O
Sigma-Aldrich
Iron(III) chloride, anhydrous, powder, ≥99.99% trace metals basis
Sigma-Aldrich
Fluoreto de fenilmetanosulfonil, ≥99.0% (T)
Sigma-Aldrich
Cloreto de sódio, BioUltra, Molecular Biology, ≥99.5% (AT)
Sigma-Aldrich
Ureia, BioXtra, pH 7.5-9.5 (20 °C, 5 M in H2O)
Sigma-Aldrich
Hydroxylamine solution, 50 wt. % in H2O, 99.999%
BRAND® 96-well microplate, U-bottom, round bottom, non-sterile
Sigma-Aldrich
Nα-Acetyl-L-lysine
Sigma-Aldrich
Aprotinin Nicotiana tobacco, >= 5TIU/mg protein, >= 98 % SDS-PAGE | 9087-70-1, recombinant, expressed in Nicotiana (tobacco), ≥5 TIU/mg protein, ≥98% (SDS-PAGE)
Sigma-Aldrich
Ethylenediaminetetraacetic acid disodium salt solution, Molecular Biology, 0.5 M in H2O, DNase, RNase, NICKase and protease, none detected