Backbone modified TBA analogues endowed with antiproliferative activity

Biochim Biophys Acta Gen Subj. 2017 May;1861(5 Pt B):1213-1221. doi: 10.1016/j.bbagen.2016.09.019. Epub 2016 Sep 20.

Abstract

Background: The thrombin binding aptamer (TBA) is endowed with antiproliferative properties but its potential development is counteracted by the concomitant anticoagulant activity.

Methods: Five oligonucleotides (ODNs) based on TBA sequence (GGTTGGTGTGGTTGG) and containing l-residues or both l-residues and inversion of polarity sites have been investigated by NMR and CD techniques for their ability to form G-quadruplex structures. Furthermore, their anticoagulant (PT assay) and antiproliferative properties (MTT assay), and their resistance in fetal bovine serum have been tested.

Results: CD and NMR data suggest that the investigated ODNs are able to form right- and left-handed G-quadruplex structures. All ODNs do not retain the anticoagulant activity characteristic of TBA but are endowed with a significant antiproliferative activity against two cancerous cell lines. Their resistance in biological environment after six days is variable, depending on the ODN.

Conclusions: A comparison between results and literature data suggests that the antiproliferative activity of the TBA analogues investigated could depends on two factors: a) biological pathways and targets different from those already identified or proposed for other antiproliferative G-quadruplex aptamers, and b) the contribution of the guanine-based degradation products.

General significance: Modified TBA analogues containing l-residues and inversion of polarity sites lose the anticoagulant activity but gain antiproliferative properties against two cancer cell lines. This article is part of a Special Issue entitled "G-quadruplex" Guest Editor: Dr. Concetta Giancola and Dr. Daniela Montesarchio.

Keywords: Antiproliferative activity; Aptamers; G-quadruplex; TBA analogues.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anticoagulants / chemistry
  • Anticoagulants / metabolism
  • Anticoagulants / pharmacology
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / pharmacology*
  • Aptamers, Nucleotide / chemistry
  • Aptamers, Nucleotide / metabolism
  • Aptamers, Nucleotide / pharmacology*
  • Base Sequence
  • Blood Coagulation / drug effects
  • Cell Proliferation / drug effects*
  • Circular Dichroism
  • Drug Stability
  • Esterases / chemistry
  • G-Quadruplexes
  • HCT116 Cells
  • Humans
  • Magnetic Resonance Spectroscopy
  • Models, Molecular
  • Neoplasms / drug therapy*
  • Neoplasms / pathology
  • Protein Binding
  • Structure-Activity Relationship
  • Thrombin / analogs & derivatives
  • Thrombin / chemistry
  • Thrombin / metabolism
  • Thrombin / pharmacology*
  • Time Factors

Substances

  • Anticoagulants
  • Antineoplastic Agents
  • Aptamers, Nucleotide
  • thrombin aptamer
  • Esterases
  • Thrombin