Institut des Biomolécules Max Mousseron, UMR 5247 CNRS, UM 1, UM 2-Faculté de Pharmacie, 15 Avenue Charles Flahault, 34093 Montpellier cedex 05 (France).
Angew Chem Int Ed Engl. 2015 May 11;54(20):5952-6. doi: 10.1002/anie.201500286. Epub 2015 Mar 20.
The development of personalized and non-invasive cancer therapies based on new targets combined with nanodevices is a major challenge in nanomedicine. In this work, the over-expression of a membrane lectin, the cation-independent mannose 6-phosphate receptor (M6PR), was specifically demonstrated in prostate cancer cell lines and tissues. To efficiently target this lectin a mannose-6-phosphate analogue was synthesized in six steps and grafted onto the surface of functionalized mesoporous silica nanoparticles (MSNs). These MSNs were used for in vitro and ex vivo photodynamic therapy to treat prostate cancer cell lines and primary cell cultures prepared from patient biopsies. The results demonstrated the efficiency of M6PR targeting for prostate cancer theranostic.
基于新靶点与纳米器件相结合的个体化与非侵入性癌症疗法的发展是纳米医学的一大挑战。在这项工作中,在前列腺癌细胞系和组织中特异性地证实了一种膜凝集素,即阳离子非依赖性甘露糖 6-磷酸受体(M6PR)的过度表达。为了有效地靶向该凝集素,我们通过六步合成了甘露糖-6-磷酸类似物,并将其接枝到功能化介孔硅纳米粒子(MSNs)的表面上。这些 MSNs 用于体外和离体光动力疗法,以治疗前列腺癌细胞系和从患者活检制备的原代细胞培养物。结果表明,M6PR 靶向前列腺癌治疗具有疗效。