| Literature DB >> 28371343 |
Christoph Englert1,2, Michael Pröhl1,2, Justyna A Czaplewska1,2, Carolin Fritzsche1,2, Elisabeth Preußger1,2, Ulrich S Schubert1,2, Anja Traeger1,2, Michael Gottschaldt1,2.
Abstract
The high affinity of GLUT5 transporter for d-fructose in breast cancer cells has been discussed intensely. In this contribution, high molar mass linear poly(ethylene imine) (LPEI) is functionalized with d-fructose moieties to combine the selectivity for the GLUT5 transporter with the delivery potential of PEI for genetic material. The four-step synthesis of a thiol-group bearing d-fructose enables the decoration of a cationic polymer backbone with d-fructose via thiol-ene photoaddition. The functionalization of LPEI is confirmed by 2D NMR techniques, elemental analysis, and size exclusion chromatography. Importantly, a d-fructose decoration of 16% renders the polymers water-soluble and eliminates the cytotoxicity of PEI in noncancer L929 cells, accompanied by a reduced unspecific cellular uptake of the genetic material. In contrast, the cytotoxicity as well as the cell specific uptake is increased for triple negative MDA-MB-231 breast cancer cells. Therefore, the introduction of d-fructose shows superior potential for cell targeting, which can be assumed to be GLUT5 dependent.Entities:
Keywords: cell-type specific uptake; d-fructose, poly(ethylene imine); nonviral gene delivery; triple-negative MDA-MB-231 breast cancer
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Year: 2017 PMID: 28371343 DOI: 10.1002/mabi.201600502
Source DB: PubMed Journal: Macromol Biosci ISSN: 1616-5187 Impact factor: 4.979