Serum-stable RNA aptamers to urokinase-type plasminogen activator blocking receptor binding.

Abstract

The serine proteinase urokinase-type plasminogen activator (uPA) is widely recognized as a potential target for anticancer therapy. Its association with cell surfaces through the uPA receptor (uPAR) is central to its function and plays an important role in cancer invasion and metastasis. In the current study, we used systematic evolution of ligands by exponential enrichment (SELEX) to select serum-stable 2'-fluoro-pyrimidine-modified RNA aptamers specifically targeting human uPA and blocking the interaction to its receptor at low nanomolar concentrations. In agreement with the inhibitory function of the aptamers, binding was found to be dependent on the presence of the growth factor domain of uPA, which mediates uPAR binding. One of the most potent uPA aptamers, upanap-12, was analyzed in more detail and could be reduced significantly in size without severe loss of its inhibitory activity. Finally, we show that the uPA-scavenging effect of the aptamers can reduce uPAR-dependent endocytosis of the uPA-PAI-1 complex and cell-surface associated plasminogen activation in cell culture experiments. uPA-scavenging 2'-fluoro-pyrimidine-modified RNA aptamers represent a novel promising principle for interfering with the pathological functions of the uPA system.

• Authors: Daniel Miotto Dupont, Jeppe Buur Madsen, Roland Karl Hartmann, Bertrand Tavitian, Frédéric Ducongé, Jørgen Kjems, Peter André Andreasen
• Journal: RNA (New York, N.Y.) (RNA) Vol. 16 Issue 12 Pg. 2360-9 (Dec 2010) ISSN: 1469-9001 [Electronic] United States
• PMID: 20962041 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)

Chemical References

• Antineoplastic Agents
• Aptamers, Nucleotide
• Multiprotein Complexes
• Plasminogen Activator Inhibitor 1
• Receptors, Urokinase Plasminogen Activator
• Urokinase-Type Plasminogen Activator

Topics

• Antineoplastic Agents (chemical synthesis, pharmacology)
• Aptamers, Nucleotide (chemical synthesis, pharmacology)
• Base Sequence
• Drug Screening Assays, Antitumor
• Drug Stability
• Endocytosis (drug effects, physiology)
• Humans
• Molecular Sequence Data
• Multiprotein Complexes (antagonists & inhibitors, metabolism)
• Plasminogen Activator Inhibitor 1 (metabolism)
• Protein Binding (drug effects)
• Protein Structure, Tertiary
• Receptors, Urokinase Plasminogen Activator (metabolism)
• Serum (metabolism)
• Substrate Specificity
• Urokinase-Type Plasminogen Activator (antagonists & inhibitors, chemistry, genetics, metabolism)