RNA Aptamers Targeting Integrin α5β1 as Probes for Cyto- and Histofluorescence in Glioblastoma

Nucleic acid aptamers are often referred to as chemical antibodies. Because they possess several advantages, like their smaller size, temperature stability, ease of chemical modification, lack of immunogenicity and toxicity, and lower cost of production, aptamers are promising tools for clinical app...

Full description

Bibliographic Details
Main Authors: Pierre Fechter, Elisabete Cruz Da Silva, Marie-Cécile Mercier, Fanny Noulet, Nelly Etienne-Seloum, Dominique Guenot, Maxime Lehmann, Romain Vauchelles, Sophie Martin, Isabelle Lelong-Rebel, Anne-Marie Ray, Cendrine Seguin, Monique Dontenwill, Laurence Choulier
Format: Article
Language:English
Published: Elsevier 2019-09-01
Series:Molecular Therapy: Nucleic Acids
Online Access:http://www.sciencedirect.com/science/article/pii/S2162253119301362
_version_ 1818155379754795008
author Pierre Fechter
Elisabete Cruz Da Silva
Marie-Cécile Mercier
Fanny Noulet
Nelly Etienne-Seloum
Dominique Guenot
Maxime Lehmann
Romain Vauchelles
Sophie Martin
Isabelle Lelong-Rebel
Anne-Marie Ray
Cendrine Seguin
Monique Dontenwill
Laurence Choulier
author_facet Pierre Fechter
Elisabete Cruz Da Silva
Marie-Cécile Mercier
Fanny Noulet
Nelly Etienne-Seloum
Dominique Guenot
Maxime Lehmann
Romain Vauchelles
Sophie Martin
Isabelle Lelong-Rebel
Anne-Marie Ray
Cendrine Seguin
Monique Dontenwill
Laurence Choulier
author_sort Pierre Fechter
collection DOAJ
description Nucleic acid aptamers are often referred to as chemical antibodies. Because they possess several advantages, like their smaller size, temperature stability, ease of chemical modification, lack of immunogenicity and toxicity, and lower cost of production, aptamers are promising tools for clinical applications. Aptamers against cell surface protein biomarkers are of particular interest for cancer diagnosis and targeted therapy. In this study, we identified and characterized RNA aptamers targeting cells expressing integrin α5β1. This αβ heterodimeric cell surface receptor is implicated in tumor angiogenesis and solid tumor aggressiveness. In glioblastoma, integrin α5β1 expression is associated with an aggressive phenotype and a decrease in patient survival. We used a complex and original hybrid SELEX (selective evolution of ligands by exponential enrichment) strategy combining protein-SELEX cycles on the recombinant α5β1 protein, surrounded by cell-SELEX cycles using two different cell lines. We identified aptamer H02, able to differentiate, in cyto- and histofluorescence assays, glioblastoma cell lines, and tissues from patient-derived tumor xenografts according to their α5 expression levels. Aptamer H02 is therefore an interesting tool for glioblastoma tumor characterization. Keywords: integrin α5β1, aptamer, SELEX, glioblastoma, cell-surface biomarker, cytofluorescence, aptahistofluorescence, therapeutic payloads delivery
first_indexed 2024-12-11T14:41:28Z
format Article
id doaj.art-30a11660aa854869a73cb126015aaf9d
institution Directory Open Access Journal
issn 2162-2531
language English
last_indexed 2024-12-11T14:41:28Z
publishDate 2019-09-01
publisher Elsevier
record_format Article
series Molecular Therapy: Nucleic Acids
spelling doaj.art-30a11660aa854869a73cb126015aaf9d2022-12-22T01:01:54ZengElsevierMolecular Therapy: Nucleic Acids2162-25312019-09-01176377RNA Aptamers Targeting Integrin α5β1 as Probes for Cyto- and Histofluorescence in GlioblastomaPierre Fechter0Elisabete Cruz Da Silva1Marie-Cécile Mercier2Fanny Noulet3Nelly Etienne-Seloum4Dominique Guenot5Maxime Lehmann6Romain Vauchelles7Sophie Martin8Isabelle Lelong-Rebel9Anne-Marie Ray10Cendrine Seguin11Monique Dontenwill12Laurence Choulier13CNRS, UMR 7242, Biotechnologie et Signalisation Cellulaire, Institut de Recherche de l’Ecole de Biotechnologie de Strasbourg, Université de Strasbourg, 67400 Illkirch-Graffenstaden, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, France; Département de Pharmacie, Centre de Lutte Contre le Cancer Paul Strauss, 67000 Strasbourg, FranceEA 3430, Progression Tumorale et Micro-environnement, Approches Translationnelles et Épidémiologie, Université de Strasbourg, 67000 Strasbourg, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7199, Laboratoire de Conception et Application de Molécules Bioactives, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, FranceCNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, France; Corresponding author: L. Choulier, CNRS, UMR 7021, Laboratoire de Bioimagerie et Pathologies, Tumoral Signaling and Therapeutic Targets, Faculté de Pharmacie, Université de Strasbourg, 67401 Illkirch, France.Nucleic acid aptamers are often referred to as chemical antibodies. Because they possess several advantages, like their smaller size, temperature stability, ease of chemical modification, lack of immunogenicity and toxicity, and lower cost of production, aptamers are promising tools for clinical applications. Aptamers against cell surface protein biomarkers are of particular interest for cancer diagnosis and targeted therapy. In this study, we identified and characterized RNA aptamers targeting cells expressing integrin α5β1. This αβ heterodimeric cell surface receptor is implicated in tumor angiogenesis and solid tumor aggressiveness. In glioblastoma, integrin α5β1 expression is associated with an aggressive phenotype and a decrease in patient survival. We used a complex and original hybrid SELEX (selective evolution of ligands by exponential enrichment) strategy combining protein-SELEX cycles on the recombinant α5β1 protein, surrounded by cell-SELEX cycles using two different cell lines. We identified aptamer H02, able to differentiate, in cyto- and histofluorescence assays, glioblastoma cell lines, and tissues from patient-derived tumor xenografts according to their α5 expression levels. Aptamer H02 is therefore an interesting tool for glioblastoma tumor characterization. Keywords: integrin α5β1, aptamer, SELEX, glioblastoma, cell-surface biomarker, cytofluorescence, aptahistofluorescence, therapeutic payloads deliveryhttp://www.sciencedirect.com/science/article/pii/S2162253119301362
spellingShingle Pierre Fechter
Elisabete Cruz Da Silva
Marie-Cécile Mercier
Fanny Noulet
Nelly Etienne-Seloum
Dominique Guenot
Maxime Lehmann
Romain Vauchelles
Sophie Martin
Isabelle Lelong-Rebel
Anne-Marie Ray
Cendrine Seguin
Monique Dontenwill
Laurence Choulier
RNA Aptamers Targeting Integrin α5β1 as Probes for Cyto- and Histofluorescence in Glioblastoma
Molecular Therapy: Nucleic Acids
title RNA Aptamers Targeting Integrin α5β1 as Probes for Cyto- and Histofluorescence in Glioblastoma
title_full RNA Aptamers Targeting Integrin α5β1 as Probes for Cyto- and Histofluorescence in Glioblastoma
title_fullStr RNA Aptamers Targeting Integrin α5β1 as Probes for Cyto- and Histofluorescence in Glioblastoma
title_full_unstemmed RNA Aptamers Targeting Integrin α5β1 as Probes for Cyto- and Histofluorescence in Glioblastoma
title_short RNA Aptamers Targeting Integrin α5β1 as Probes for Cyto- and Histofluorescence in Glioblastoma
title_sort rna aptamers targeting integrin α5β1 as probes for cyto and histofluorescence in glioblastoma
url http://www.sciencedirect.com/science/article/pii/S2162253119301362
work_keys_str_mv AT pierrefechter rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT elisabetecruzdasilva rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT mariececilemercier rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT fannynoulet rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT nellyetienneseloum rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT dominiqueguenot rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT maximelehmann rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT romainvauchelles rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT sophiemartin rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT isabellelelongrebel rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT annemarieray rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT cendrineseguin rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT moniquedontenwill rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma
AT laurencechoulier rnaaptamerstargetingintegrina5b1asprobesforcytoandhistofluorescenceinglioblastoma