Aptamer selection and applications for breast cancer diagnostics and therapy

J Nanobiotechnology. 2017 Nov 13;15(1):81. doi: 10.1186/s12951-017-0311-4.

Abstract

Aptamers are short non-coding, single-stranded oligonucleotides (RNA or DNA) developed through Systematic Evolution of Ligands by Exponential enrichment (SELEX) in vitro. Similar to antibodies, aptamers can bind to specific targets with high affinity, and are considered promising therapeutic agents as they have several advantages over antibodies, including high specificity, stability, and non-immunogenicity. Furthermore, aptamers can be produced at a low cost and easily modified, and are, therefore, called "chemical antibodies". In the past years, a variety of aptamers specifically bound to both breast cancer biomarkers and cells had been selected. Besides, taking advantage of nanomaterials, there were a number of aptamer-nanomaterial conjugates been developed and widely investigated for diagnostics and targeted therapy of breast cancer. In this short review, we first present a systematical review of various aptamer selection methods. Then, various aptamer-based diagnostic and therapeutic strategies of breast cancer were provided. Finally, the current problems, challenges, and future perspectives in the field were thoroughly discussed.

Keywords: Aptamer; Breast cancer; Diagnosis; SELEX; Targeted therapy.

Publication types

  • Review

MeSH terms

  • Antibiotics, Antineoplastic / chemistry
  • Antibiotics, Antineoplastic / therapeutic use
  • Aptamers, Nucleotide / chemical synthesis
  • Aptamers, Nucleotide / pharmacokinetics
  • Aptamers, Nucleotide / therapeutic use*
  • Biomarkers, Tumor / genetics*
  • Biomarkers, Tumor / metabolism
  • Breast Neoplasms / diagnosis*
  • Breast Neoplasms / genetics
  • Breast Neoplasms / pathology
  • Breast Neoplasms / therapy*
  • Cell Line, Tumor
  • Doxorubicin / chemistry
  • Doxorubicin / therapeutic use*
  • Epithelial Cell Adhesion Molecule / genetics
  • Epithelial Cell Adhesion Molecule / metabolism
  • Estrogen Receptor alpha / genetics
  • Estrogen Receptor alpha / metabolism
  • Female
  • Gene Expression
  • Humans
  • Ligands
  • Molecular Targeted Therapy / methods
  • Nanotubes
  • Protein Binding
  • Receptor, ErbB-2 / genetics
  • Receptor, ErbB-2 / metabolism
  • SELEX Aptamer Technique*

Substances

  • Antibiotics, Antineoplastic
  • Aptamers, Nucleotide
  • Biomarkers, Tumor
  • EPCAM protein, human
  • ESR1 protein, human
  • Epithelial Cell Adhesion Molecule
  • Estrogen Receptor alpha
  • Ligands
  • Doxorubicin
  • ERBB2 protein, human
  • Receptor, ErbB-2