| Literature DB >> 31454552 |
Maha Hafsi1, Sandra Preveral2, Christopher Hoog3, Joel Hérault4, Géraldine Adryanczyk Perrier2, Christopher T Lefèvre2, Hervé Michel5, David Pignol2, Jérôme Doyen4, Thierry Pourcher6, Olivier Humbert7, Juliette Thariat8, Béatrice Cambien9.
Abstract
Although chemically synthesized ferro/ferrimagnetic nanoparticles have attracted great attention in cancer theranostics, they lack radio-enhancement efficacy due to low targeting and internalization ability. Herein, we investigated the potential of RGD-tagged magnetosomes, bacterial biogenic magnetic nanoparticles naturally coated with a biological membrane and genetically engineered to express an RGD peptide, as tumor radioenhancers for conventional radiotherapy and proton therapy. Although native and RGD-magnetosomes similarly enhanced radiation-induced damage to plasmid DNA, RGD-magnetoprobes were able to boost the efficacy of radiotherapy to a much larger extent than native magnetosomes both on cancer cells and in tumors. Combined to magnetosomes@RGD, proton therapy exceeded the efficacy of X-rays at equivalent doses. Also, increased secondary emissions were measured after irradiation of magnetosomes with protons versus photons. Our results indicate the therapeutic advantage of using functionalized magnetoparticles to sensitize tumors to both X-rays and protons and strengthen the case for developing biogenic magnetoparticles for multimodal nanomedicine in cancer therapy. Published by Elsevier Inc.Entities:
Keywords: Proton therapy; RGD functionalized magnetosome; Radioenhancement; Radiotherapy
Year: 2019 PMID: 31454552 DOI: 10.1016/j.nano.2019.102084
Source DB: PubMed Journal: Nanomedicine ISSN: 1549-9634 Impact factor: 5.307