Chlorin e6 Conjugated Interleukin-6 Receptor Aptamers Selectively Kill Target Cells Upon Irradiation

Photodynamic therapy (PDT) uses the therapeutic properties of light in combination with certain chemicals, called photosensitizers, to successfully treat brain, breast, prostate, and skin cancers. To improve PDT, current research focuses on the development of photosensitizers to specifically target...

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Main Authors: Sven Kruspe, Cindy Meyer, Ulrich Hahn
Format: Article
Language:English
Published: Elsevier 2014-01-01
Series:Molecular Therapy: Nucleic Acids
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2162253116302827
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spelling doaj-00cc80d683e149f4bc2237b18cfdbf432020-11-25T02:02:30ZengElsevierMolecular Therapy: Nucleic Acids2162-25312014-01-013C10.1038/mtna.2013.70Chlorin e6 Conjugated Interleukin-6 Receptor Aptamers Selectively Kill Target Cells Upon IrradiationSven Kruspe0Cindy Meyer1Ulrich Hahn2Chemistry Department, MIN-Faculty, Institute for Biochemistry and Molecular Biology, Hamburg University, Hamburg, GermanyCurrent address: Howard Hughes Medical Institute, Laboratory of RNA Molecular Biology, The Rockefeller University, New York, USAChemistry Department, MIN-Faculty, Institute for Biochemistry and Molecular Biology, Hamburg University, Hamburg, GermanyPhotodynamic therapy (PDT) uses the therapeutic properties of light in combination with certain chemicals, called photosensitizers, to successfully treat brain, breast, prostate, and skin cancers. To improve PDT, current research focuses on the development of photosensitizers to specifically target cancer cells. In the past few years, aptamers have been developed to directly deliver cargo molecules into target cells. We conjugated the photosensitizer chlorin e6 (ce6) with a human interleukin-6 receptor (IL-6R) binding RNA aptamer, AIR-3A yielding AIR-3A-ce6 for application in high efficient PDT. AIR-3A-ce6 was rapidly and specifically internalized by IL-6R presenting (IL-6R+) cells. Upon light irradiation, targeted cells were selectively killed, while free ce6 did not show any toxic effect. Cells lacking the IL-6R were also not affected by AIR-3A-ce6. With this approach, we improved the target specificity of ce6-mediated PDT. In the future, other tumor-specific aptamers might be used to selectively localize photosensitizers into cells of interest and improve the efficacy and specificity of PDT in cancer and other diseases.http://www.sciencedirect.com/science/article/pii/S2162253116302827aptamershuman interleukin-6 receptorphotodynamic therapyreceptor mediated endocytosis
collection DOAJ
language English
format Article
sources DOAJ
author Sven Kruspe
Cindy Meyer
Ulrich Hahn
spellingShingle Sven Kruspe
Cindy Meyer
Ulrich Hahn
Chlorin e6 Conjugated Interleukin-6 Receptor Aptamers Selectively Kill Target Cells Upon Irradiation
Molecular Therapy: Nucleic Acids
aptamers
human interleukin-6 receptor
photodynamic therapy
receptor mediated endocytosis
author_facet Sven Kruspe
Cindy Meyer
Ulrich Hahn
author_sort Sven Kruspe
title Chlorin e6 Conjugated Interleukin-6 Receptor Aptamers Selectively Kill Target Cells Upon Irradiation
title_short Chlorin e6 Conjugated Interleukin-6 Receptor Aptamers Selectively Kill Target Cells Upon Irradiation
title_full Chlorin e6 Conjugated Interleukin-6 Receptor Aptamers Selectively Kill Target Cells Upon Irradiation
title_fullStr Chlorin e6 Conjugated Interleukin-6 Receptor Aptamers Selectively Kill Target Cells Upon Irradiation
title_full_unstemmed Chlorin e6 Conjugated Interleukin-6 Receptor Aptamers Selectively Kill Target Cells Upon Irradiation
title_sort chlorin e6 conjugated interleukin-6 receptor aptamers selectively kill target cells upon irradiation
publisher Elsevier
series Molecular Therapy: Nucleic Acids
issn 2162-2531
publishDate 2014-01-01
description Photodynamic therapy (PDT) uses the therapeutic properties of light in combination with certain chemicals, called photosensitizers, to successfully treat brain, breast, prostate, and skin cancers. To improve PDT, current research focuses on the development of photosensitizers to specifically target cancer cells. In the past few years, aptamers have been developed to directly deliver cargo molecules into target cells. We conjugated the photosensitizer chlorin e6 (ce6) with a human interleukin-6 receptor (IL-6R) binding RNA aptamer, AIR-3A yielding AIR-3A-ce6 for application in high efficient PDT. AIR-3A-ce6 was rapidly and specifically internalized by IL-6R presenting (IL-6R+) cells. Upon light irradiation, targeted cells were selectively killed, while free ce6 did not show any toxic effect. Cells lacking the IL-6R were also not affected by AIR-3A-ce6. With this approach, we improved the target specificity of ce6-mediated PDT. In the future, other tumor-specific aptamers might be used to selectively localize photosensitizers into cells of interest and improve the efficacy and specificity of PDT in cancer and other diseases.
topic aptamers
human interleukin-6 receptor
photodynamic therapy
receptor mediated endocytosis
url http://www.sciencedirect.com/science/article/pii/S2162253116302827
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