Breast Cancer Classification Based on Proteotypes Obtained by SWATH Mass Spectrometry

Cell Rep. 2019 Jul 16;28(3):832-843.e7. doi: 10.1016/j.celrep.2019.06.046.

Abstract

Accurate classification of breast tumors is vital for patient management decisions and enables more precise cancer treatment. Here, we present a quantitative proteotyping approach based on sequential windowed acquisition of all theoretical fragment ion spectra (SWATH) mass spectrometry and establish key proteins for breast tumor classification. The study is based on 96 tissue samples representing five conventional breast cancer subtypes. SWATH proteotype patterns largely recapitulate these subtypes; however, they also reveal varying heterogeneity within the conventional subtypes, with triple negative tumors being the most heterogeneous. Proteins that contribute most strongly to the proteotype-based classification include INPP4B, CDK1, and ERBB2 and are associated with estrogen receptor (ER) status, tumor grade status, and HER2 status. Although these three key proteins exhibit high levels of correlation with transcript levels (R > 0.67), general correlation did not exceed R = 0.29, indicating the value of protein-level measurements of disease-regulated genes. Overall, this study highlights how cancer tissue proteotyping can lead to more accurate patient stratification.

Keywords: SWATH-MS; breast cancer; data independent acquisition; proteomics; tissue; transcriptomics; tumor classification.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Breast Neoplasms / classification*
  • Breast Neoplasms / metabolism
  • Breast Neoplasms / pathology
  • CDC2 Protein Kinase / genetics
  • CDC2 Protein Kinase / metabolism*
  • Female
  • High-Throughput Screening Assays
  • Humans
  • Phosphoric Monoester Hydrolases / genetics
  • Phosphoric Monoester Hydrolases / metabolism*
  • Proteome / analysis*
  • Proteome / metabolism
  • Proteomics / methods*
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism*
  • Receptors, Estrogen / metabolism
  • Tandem Mass Spectrometry / methods*

Substances

  • Proteome
  • Receptors, Estrogen
  • ERBB2 protein, human
  • Receptor, ErbB-2
  • CDC2 Protein Kinase
  • CDK1 protein, human
  • Phosphoric Monoester Hydrolases
  • phosphatidylinositol-3,4-bisphosphate 4-phosphatase