A specific photoimmunotheranostics agent to detect and eliminate skin cancer cells expressing EGFR

Verena von Felbert, Dirk Bauerschlag, Nicolai Maass, Karen Bräutigam, Ivo Meinhold-Heerlein, Mira Woitok, Stefan Barth, Ahmad Fawzi Hussain*

*Korrespondierende/r Autor/-in für diese Arbeit
20 Zitate (Scopus)


Purpose: The term “theranostics” represents a new paradigm in medicine especially for cancer treatment. This term was coined by Funkhouser in 2002 and defines a reagent that combines therapeutic and diagnostic properties. It is widely believed that theranostics agents will have considerable impact on healthcare before, during, and after disease by improving cancer prognosis and management simultaneously. Current theranostics approaches still rely on passive tumor targeting strategies, which have scattergun effects and tend to damage both neoplastic and non-neoplastic cells. Methods: Here we describe a simple, controlled, and efficient method to generate homogeneous photoimmunotheranostics reagents. This method combines molecular optical imaging, photodynamic therapy, and immunotherapy using SNAP-tag technology. SNAP-tag is a derivative of the O(6)-alkylguanine-DNA alkyltransferase (AGT) which has the ability to efficiently conjugate to O(6)-benzylguanine (BG) molecules under physiological conditions depending on its folding pattern. Results: The theranostics agent was able to specifically recognize various epidermal growth factor receptor (EGFR)-expressing skin cancer cell lines using flow cytometry analysis and confocal microscopy and eliminate them at EC50’s of 32–55 nM. Conclusions: These experiments provide a framework for using SNAP-tag technology to generate homogeneous photoimmunotheranostics reagents with unified pharmacokinetic and therapeutic profiles. Furthermore, the reagent generated in this work could be used to simultaneously monitor and suppress the growth of skin squamous carcinoma and melanoma cells expressing EGFR.

ZeitschriftJournal of Cancer Research and Clinical Oncology
Seiten (von - bis)1003-1011
PublikationsstatusVeröffentlicht - 01.05.2016


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