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Pharmaceuticals 2016, 9(2), 29;

Improved Aptamers for the Diagnosis and Potential Treatment of HER2-Positive Cancer

Radiobiology Unit, Belgian Nuclear Research Centre (SCK•CEN), 2400 Mol, Belgium
Cyclotron Research Centre, University of Liège, 4000 Liège, Belgium
NeoVentures Biotechnology Inc., London, N6A 1A1 ON, Canada
Author to whom correspondence should be addressed.
Academic Editor: Alfredo Berzal-Herranz
Received: 20 February 2016 / Revised: 9 May 2016 / Accepted: 10 May 2016 / Published: 19 May 2016
(This article belongs to the Special Issue Aptamers: Biomedical Interest and Applications)
View Full-Text   |   Download PDF [4066 KB, uploaded 19 May 2016]   |  


Aptamers provide a potential source of alternative targeting molecules for existing antibody diagnostics and therapeutics. In this work, we selected novel DNA aptamers targeting the HER2 receptor by an adherent whole-cell SELEX approach. Individual aptamers were identified by next generation sequencing and bioinformatics analysis. Two aptamers, HeA2_1 and HeA2_3, were shown to bind the HER2 protein with affinities in the nanomolar range. In addition, both aptamers were able to bind with high specificity to HER2-overexpressing cells and HER2-positive tumor tissue samples. Furthermore, we demonstrated that aptamer HeA2_3 is being internalized into cancer cells and has an inhibitory effect on cancer cell growth and viability. In the end, we selected novel DNA aptamers with great potential for the diagnosis and possible treatment of HER2-positive cancer. View Full-Text
Keywords: aptamer; DNA; HER2; diagnosis; therapeutics; cancer aptamer; DNA; HER2; diagnosis; therapeutics; cancer

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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

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Gijs, M.; Penner, G.; Blackler, G.B.; Impens, N.R.; Baatout, S.; Luxen, A.; Aerts, A.M. Improved Aptamers for the Diagnosis and Potential Treatment of HER2-Positive Cancer. Pharmaceuticals 2016, 9, 29.

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