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  • Proteogenomic Landscape of Breast Cancer Tumorigenesis and Targeted Therapy.

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
ABSTRACT

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.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Phosphatase Inhibitor Cocktail 3, DMSO solution
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Phenylmethanesulfonyl fluoride, ≥99.0% (T)
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Iron(III) chloride, anhydrous, powder, ≥99.99% trace metals basis
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Nα-Acetyl-L-lysine
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Phosphatase Inhibitor Cocktail 2, aqueous solution (dark coloration may develop upon storage, which does not affect the activity)
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Sodium chloride, BioUltra, for molecular biology, ≥99.5% (AT)
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Aprotinin Nicotiana tobacco, >= 5TIU/mg protein, >= 98 % SDS-PAGE | 9087-70-1, recombinant, expressed in Nicotiana (tobacco), ≥5 TIU/mg protein, ≥98% (SDS-PAGE)
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Hydroxylamine solution, 50 wt. % in H2O, 99.999%
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Hydroxylamine solution, 50 wt. % in H2O
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Urea, BioXtra, pH 7.5-9.5 (20 °C, 5 M in H2O)
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Iodoacetamide, Single use vial of 56 mg
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Sodium fluoride, BioXtra, ≥99%
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Ethylenediaminetetraacetic acid disodium salt solution, for molecular biology, 0.5 M in H2O, DNase, RNase, NICKase and protease, none detected
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Trifluoroacetic acid, suitable for HPLC, ≥99.0%
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Formic acid, reagent grade, ≥95%
BRAND® 96-well microplate, U-bottom, round bottom, non-sterile
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Potassium phosphate dibasic, ACS reagent, ≥98%
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Potassium phosphate monobasic, ACS reagent, ≥99.0%
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Sodium phosphate dibasic, ACS reagent, ≥99.0%
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Ammonium hydroxide solution, 28% NH3 in H2O, ≥99.99% trace metals basis