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 |
|
|