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Antitumor effects of (32)P-chromic-poly (L-lactide) brachytherapy in nude mice with human prostate cancer

The aim of the present study was to investigate the antitumor effects and tissue distribution of (32)P-chromic-poly (L-lactide) ((32)P-CP-PLLA) in nude mice with human prostate cancer. Tumor models were obtained by transplantation of PC-3M tumor cells into male BALB/c nude mice. Animals were randoml...

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Detalles Bibliográficos
Autores principales: SUN, LIUJING, ZHU, XISHAN, XU, LONGBAO, WANG, ZIZHENG, SHAO, GUOQIANG, ZHAO, JUN
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3789100/
https://www.ncbi.nlm.nih.gov/pubmed/24137391
http://dx.doi.org/10.3892/ol.2013.1443
Descripción
Sumario:The aim of the present study was to investigate the antitumor effects and tissue distribution of (32)P-chromic-poly (L-lactide) ((32)P-CP-PLLA) in nude mice with human prostate cancer. Tumor models were obtained by transplantation of PC-3M tumor cells into male BALB/c nude mice. Animals were randomly divided into control, (32)P-chromic phosphate ((32)P-CP) colloid and (32)P-CP-PLLA groups (all n=20). A series of indices were investigated, including apoptosis of tumor cells, rate of apoptosis, expression of caspase 3 and 8, biodistribution and intratumoral concentration of (32)P-CP-PLLA, intensity of radioactivity, tumor volume and microvessel density (MVD). Highly concentrated radioactivity of (32)P-CP-PLLA in the tumor mass was detected by single photon emission computed tomography (SPECT) scanning. The residual activities of the (32)P-CP-PLLA and (32)P-CP colloid groups were 3.02±0.32 and 1.76±0.31 MBq, respectively, on day 14 following treatment. The tumor inhibition rates were 67.24±3.55 and 55.92±7.65%, respectively (P<0.01). Necrotic changes, in conjunction with apoptosis, were observed in the treatment group. MVD values for the (32)P-CP-PLLA and (32)P-CP colloid groups were 28.24±10.07 and 36.15±11.06, respectively. (32)P-CP-PLLA showed an excellent capacity for killing tumor cells, inducing apoptosis and inhibiting angiogenesis.