Dose Rate Effects on the Selective Radiosensitization of Prostate Cells by GRPR-Targeted Gold Nanoparticles

被引:11
作者
Marques, Ana [1 ,2 ]
Belchior, Ana [2 ]
Silva, Francisco [2 ]
Marques, Fernanda [2 ,3 ]
Campello, Maria Paula Cabral [2 ,3 ]
Pinheiro, Teresa [3 ,4 ]
Santos, Pedro [2 ]
Santos, Luis [5 ]
Matos, Antonio P. A. [6 ]
Paulo, Antonio [2 ,3 ]
机构
[1] Univ Lisbon, Inst Super Tecn, Dept Fis, Ave Rovisco Pais, P-1049001 Lisbon, Portugal
[2] Univ Lisbon, Inst Super Tecn, Ctr Ciencias Tecnol Nucl, Campus Tecnol Nucl,Estrada Nacl 10 Km 1397, P-2695066 Bobadela, Portugal
[3] Univ Lisbon, Inst Super Tecn, Dept Engn & Ciencias Nucl, Av Rovisco Pais 1, P-1049001 Lisbon, Portugal
[4] Univ Lisbon, Inst Bioengn Biociencias, Inst Super Tecn, Ave Rovisco Pais 1, P-1049001 Lisbon, Portugal
[5] Univ Lisbon, Inst Super Tecn, Lab Metrol, Av. Rovisco Pais 1, P-1049001 Lisbon, Portugal
[6] Ctr Invest Interdisciplinar Egas Moniz, Campus Univ, P-2829511 Caparica, Portugal
关键词
radiotherapy; radiosensitizer; gold nanoparticles; prostate cancer; CALCIUM MOBILIZATION; CANCER; MECHANISMS; IRRADIATION; SIZE; RADIOTHERAPY; SURVIVAL;
D O I
10.3390/ijms23095279
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
For a while, gold nanoparticles (AuNPs) have been recognized as potential radiosensitizers in cancer radiation therapy, mainly due to their physical properties, making them appealing for medical applications. Nevertheless, the performance of AuNPs as radiosensitizers still raises important questions that need further investigation. Searching for selective prostate (PCa) radiosensitizing agents, we studied the radiosensitization capability of the target-specific AuNP-BBN in cancer versus non-cancerous prostate cells, including the evaluation of dose rate effects in comparison with non-targeted counterparts (AuNP-TDOTA). PCa cells were found to exhibit increased AuNP uptake when compared to non-tumoral ones, leading to a significant loss of cellular proliferation ability and complex DNA damage, evidenced by the occurrence of multiple micronucleus per binucleated cell, in the case of PC3 cells irradiated with 2 Gy of gamma-rays, after incubation with AuNP-BBN. Remarkably, the treatment of the PC3 cells with AuNP-BBN led to a much stronger influence of the dose rate on the cellular survival upon gamma-photon irradiation, as well as on their genomic instability. Overall, AuNP-BBN emerged in this study as a very promising nanotool for the efficient and selective radiosensitization of human prostate cancer PC3 cells, therefore deserving further preclinical evaluation in adequate animal models for prostate cancer radiotherapy.
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页数:18
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