Use of a conformational switching aptamer for rapid and specific ex vivo identification of central nervous system lymphoma in a xenograft model

PLoS One. 2015 Apr 15;10(4):e0123607. doi: 10.1371/journal.pone.0123607. eCollection 2015.

Abstract

Improved tools for providing specific intraoperative diagnoses could improve patient care. In neurosurgery, intraoperatively differentiating non-operative lesions such as CNS B-cell lymphoma from operative lesions can be challenging, often necessitating immunohistochemical (IHC) procedures which require up to 24-48 hours. Here, we evaluate the feasibility of generating rapid ex vivo specific labeling using a novel lymphoma-specific fluorescent switchable aptamer. Our B-cell lymphoma-specific switchable aptamer produced only low-level fluorescence in its unbound conformation and generated an 8-fold increase in fluorescence once bound to its target on CD20-positive lymphoma cells. The aptamer demonstrated strong binding to B-cell lymphoma cells within 15 minutes of incubation as observed by flow cytometry. We applied the switchable aptamer to ex vivo xenograft tissue harboring B-cell lymphoma and astrocytoma, and within one hour specific visual identification of lymphoma was routinely possible. In this proof-of-concept study in human cell culture and orthotopic xenografts, we conclude that a fluorescent switchable aptamer can provide rapid and specific labeling of B-cell lymphoma, and that developing aptamer-based labeling approaches could simplify tissue staining and drastically reduce time to histopathological diagnoses compared with IHC-based methods. We propose that switchable aptamers could enhance expeditious, accurate intraoperative decision-making.

MeSH terms

  • Animals
  • Aptamers, Nucleotide / chemistry*
  • Astrocytoma / chemistry
  • Astrocytoma / genetics
  • Astrocytoma / metabolism
  • Cell Line, Tumor
  • Central Nervous System Neoplasms / chemistry
  • Central Nervous System Neoplasms / diagnosis*
  • Central Nervous System Neoplasms / surgery
  • Flow Cytometry
  • Fluorescent Dyes / chemistry
  • Fluorometry
  • Humans
  • Intraoperative Period
  • Luminescent Proteins / genetics
  • Luminescent Proteins / metabolism
  • Lymphoma, B-Cell / chemistry
  • Lymphoma, B-Cell / diagnosis*
  • Lymphoma, B-Cell / surgery
  • Microscopy, Confocal
  • Molecular Diagnostic Techniques / methods
  • Nucleic Acid Conformation*
  • Rats, Nude
  • Red Fluorescent Protein
  • Reproducibility of Results
  • Sensitivity and Specificity
  • Transplantation, Heterologous

Substances

  • Aptamers, Nucleotide
  • Fluorescent Dyes
  • Luminescent Proteins

Grants and funding

These authors have no support or funding to report.