Nanobodies as Versatile Tools to Understand, Diagnose, Visualize and Treat Cancer

EBioMedicine. 2016 Jun:8:40-48. doi: 10.1016/j.ebiom.2016.04.028. Epub 2016 Apr 30.

Abstract

Since their discovery, nanobodies have been used extensively in the fields of research, diagnostics and therapy. These antigen binding fragments, originating from Camelid heavy-chain antibodies, possess unusual hallmarks in terms of (small) size, stability, solubility and specificity, hence allowing cost-effective production and sometimes outperforming monoclonal antibodies. In this review, we evaluate the current status of nanobodies to study, diagnose, visualize or inhibit cancer-specific proteins and processes. Nanobodies are highly adaptable tools for cancer research as they enable specific modulation of targets, enzymatic and non-enzymatic proteins alike. Molecular imaging studies benefit from the rapid, homogeneous tumor accumulation of nanobodies and their fast blood clearance, permitting previously unattainable fast tumor visualization. Moreover, they are endowed with considerable therapeutic potential as inhibitors of receptor-ligand pairs and deliverers of drugs or drug-loaded nanoparticles towards tumors. More in vivo and clinical studies are however eagerly awaited to unleash their full potential.

Keywords: Cancer; Heavy chain antibody; Nanobody; Single domain antibody; VHH.

Publication types

  • Review

MeSH terms

  • Animals
  • Biomarkers, Tumor / immunology
  • Biomarkers, Tumor / metabolism
  • Contrast Media / chemistry
  • Drug Carriers / chemistry
  • Humans
  • Neoplasms / diagnosis
  • Neoplasms / diagnostic imaging
  • Neoplasms / drug therapy*
  • Neoplasms / pathology
  • Protein Domains / immunology
  • Receptors, Cell Surface / chemistry
  • Receptors, Cell Surface / immunology
  • Receptors, Cell Surface / metabolism
  • Single-Domain Antibodies / immunology
  • Single-Domain Antibodies / therapeutic use*
  • Tomography, Emission-Computed

Substances

  • Biomarkers, Tumor
  • Contrast Media
  • Drug Carriers
  • Receptors, Cell Surface
  • Single-Domain Antibodies