首页 | 本学科首页   官方微博 | 高级检索  
     


Multifunctional targeted therapy system based on 99mTc/177Lu‐labeled gold nanoparticles‐Tat(49–57)‐Lys3‐bombesin internalized in nuclei of prostate cancer cells
Authors:Nallely Jiménez‐Mancilla  Guillermina Ferro‐Flores  Clara Santos‐Cuevas  Blanca Ocampo‐García  Myrna Luna‐Gutiérrez  Erika Azorín‐Vega  Keila Isaac‐Olivé  Miguel Camacho‐López  Eugenio Torres‐García
Affiliation:1. Departamento de Materiales Radiactivos, Instituto Nacional de Investigaciones Nucleares, , Estado de México, Mexico;2. Facultad de Medicina, Universidad Autónoma del Estado de México, , Estado de México, Mexico
Abstract:Radiolabeled gold nanoparticles may function simultaneously as radiotherapy and thermal ablation systems. The gastrin‐releasing peptide receptor (GRP‐r) is overexpressed in prostate cancer, and Lys3‐bombesin is a peptide that binds with high affinity to the GRP‐r. HIV Tat(49–57) is a cell‐penetrating peptide that reaches the DNA. In cancer cells, 177Lu shows efficient crossfire effect, whereas 99mTc that is internalized in the cancer cell nuclei acts as an effective system of targeted radiotherapy because of the biological Auger effect. The aim of this research was to evaluate the in vitro potential of 99mTc‐labeled and 177Lu‐labeled gold nanoparticles conjugated to Tat(49–57)‐Lys3‐bombesin peptides (99mTc/177Lu‐AuNP‐Tat‐BN) as a plasmonic photothermal therapy and targeted radiotherapy system in PC3 prostate cancer cells. Peptides were conjugated to AuNPs (5 nm) by spontaneous reaction with the thiol group of cysteine (Cys). The effect on PC3 cell viability after laser heating of the AuNP‐Tat‐BN incubated with the cancer cells was conducted using an Nd:YAG laser pulsed for 5 ns at 532 nm (0.65 W/cm2). For the 99mTc/177Lu‐AuNP‐Tat‐BN to be obtained, the 177Lu‐DOTA‐Gly‐Gly‐Cys and 99mTc‐HYNIC‐octreotide radiopeptides were first prepared and added simultaneously to a solution of AuNP‐Tat‐BN. 99mTc/177Lu‐AuNP‐Tat‐BN (20 Bq/cell) was incubated with PC3 cells, and the effect on the cell proliferation was evaluated after 3 days. Fluorescence images of 99mTc/177Lu‐AuNP‐Tat‐BN internalized in nuclei of PC3 were also obtained. After laser irradiation, the presence of AuNP‐Tat‐BN caused a significant increase in the temperature of the medium (46.4 vs 39.5 °C of that without AuNP) resulting in a significant decrease in PC3 cell viability down to 1.3%. After treatment with 99mTc/177Lu‐AuNP‐Tat‐BN, the PC3 cell proliferation was inhibited. The nanosystem exhibited properties suitable for plasmonic photothermal therapy and targeted radiotherapy in the treatment of prostate cancer.
Keywords:gold nanoparticles  radiolabeled nanoparticles  Lys3‐bombesin  radiolabeled peptides  nanoparticle‐peptide  Tat peptide  lutetium‐177  technetium‐99m
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号