Cancer cell profiling by barcoding allows multiplexed protein analysis in fine-needle aspirates

Sci Transl Med. 2014 Jan 15;6(219):219ra9. doi: 10.1126/scitranslmed.3007361.

Abstract

Immunohistochemistry-based clinical diagnoses require invasive core biopsies and use a limited number of protein stains to identify and classify cancers. We introduce a technology that allows analysis of hundreds of proteins from minimally invasive fine-needle aspirates (FNAs), which contain much smaller numbers of cells than core biopsies. The method capitalizes on DNA-barcoded antibody sensing, where barcodes can be photocleaved and digitally detected without any amplification steps. After extensive benchmarking in cell lines, this method showed high reproducibility and achieved single-cell sensitivity. We used this approach to profile ~90 proteins in cells from FNAs and subsequently map patient heterogeneity at the protein level. Additionally, we demonstrate how the method could be used as a clinical tool to identify pathway responses to molecularly targeted drugs and to predict drug response in patient samples. This technique combines specificity with ease of use to offer a new tool for understanding human cancers and designing future clinical trials.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Antibodies / immunology
  • Biopsy, Fine-Needle
  • Cell Line, Tumor
  • DNA / metabolism
  • Humans
  • Neoplasm Proteins / analysis*
  • Neoplasm Proteins / metabolism
  • Neoplasms / metabolism*
  • Phosphatidylinositol 3-Kinases / metabolism
  • Phosphoinositide-3 Kinase Inhibitors
  • Protein Array Analysis / methods*
  • Protein Kinase Inhibitors / pharmacology
  • Reproducibility of Results
  • Signal Transduction / drug effects
  • Single-Cell Analysis

Substances

  • Antibodies
  • Neoplasm Proteins
  • Phosphoinositide-3 Kinase Inhibitors
  • Protein Kinase Inhibitors
  • DNA