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Träfflista för sökning "WFRF:(Rudqvist Nils) ;pers:(Ahlman Håkan 1947)"

Sökning: WFRF:(Rudqvist Nils) > Ahlman Håkan 1947

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1.
  • Dalmo, Johanna, et al. (författare)
  • Biodistribution of 177Lu-octreotate and 111In-minigastrin in female nude mice transplanted with human medullary thyroid carcinoma GOT2.
  • 2012
  • Ingår i: Oncology reports. - : Spandidos Publications. - 1791-2431 .- 1021-335X. ; 27:1, s. 174-181
  • Tidskriftsartikel (refereegranskat)abstract
    • To be able to evaluate new radiopharmaceuticals and optimize diagnostic and therapeutic procedures, relevant animal models are required. The aim of this study was to evaluate the medullary thyroid carcinoma GOT2 animal model by analyzing the biodistribution of 177Lu-octreotate and 111In-minigastrin (MG0). BALB/c nude mice, subcutaneously transplanted with GOT2, were intravenously injected with either 177Lu-octreotate or 111In-MG0, with or without excess of unlabeled human minigastrin simultaneously with 111In-MG0. Animals were sacrificed 1-7 days after injection in the 177Lu-octreotate study and 1h after injection of 111In-MG0. The activity concentrations in organs and tissues were determined and mean absorbed doses from 177Lu were calculated. There was a specific tumor uptake of either 177Lu-octreotate or 111In-MG0. 177Lu-octreotate samples showed high activity concentrations in tissues expressing somatostatin receptors (SSTR). For both radiopharmaceuticals the highest activity concentrations were found in the kidneys. Compared to results from similar studies in mice with another MTC cell line (TT) the biodistribution was favorable (higher tumor uptake) for the GOT2 model, while compared to other animal models expressing SSTR, the tumor uptake of 177Lu-octreotate was modest. In conclusion, the GOT2 animal model is a valuable model for evaluation and optimization of diagnostic and therapeutic procedures using radiolabeled somatostatin, CCK2 and gastrin analogues prior to clinical studies.
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  • Larsson, Maria, 1972, et al. (författare)
  • Kidney toxicity in mice treated with 177Lu-octreotate
  • 2012
  • Ingår i: 25th Annual Congress on European Association of Nuclear Medicine, Milano, Italy, October 27-31, 2012 . (European Journal of Nuclear Medicine and Molecular Imaging). - 1619-7070.
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)
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4.
  • Spetz, Johan, et al. (författare)
  • Effects of internal irradiation from 177Lu-octreotate on gene expression in GOT1 midgut carcinoid in nude mice
  • 2012
  • Ingår i: 58th Annual Meeting of the Radiation Research Society, San Juan, Puerto Rico, September 30 - October 3, 2012.
  • Konferensbidrag (övrigt vetenskapligt/konstnärligt)abstract
    • Radionuclide therapy using the somatostatin analog 177Lu-octreotate is promising for treatment of malignant neuroendocrine tumors, e.g. carcinoids and endocrine pancreatic tumors, with high expression of somatostatin receptors. Little is known about molecular mechanisms after irradiation of neuroendocrine tumors. The aim of this study was to investigate the regulation of gene expression in the human midgut carcinoma cell line GOT1. Female GOT1 bearing BALB/c nude mice were intravenously injected with 7 MBq 177Lu-octreotate. After 24 hours, all animals were sacrificed and tumors were excised. Radioactivity measurements were performed on the tumor tissues and absorbed doses were determined to about 2 Gy. Total RNA was extracted from the tumors and processed using Illumina MouseRef-8 Whole-Genome Expression Beadchips. Nexus Expression 2.0 was used for data analysis of both regulated genes and biological processes. The data was compared with that of a control group receiving only NaCl solution intravenously. Analysis revealed a strong up-regulation of four genes after irradiation, compared to controls. These genes were identified and classified using Gene Ontology terms. Two of the genes (CXCL9, encoding a cytokine and the SERPINA3, encoding a serpin peptidase inhibitor) were found to be associated with e.g. immune and inflammatory response, while the other two (ACTA1, encoding actin and MYL1, encoding myosin light chain 1/3) were associated with e.g. muscle contraction. ACTA1 was also found to be associated to cell growth. These preliminary results show that 177Lu-octreotate caused a significant impact on gene expression of a few genes in GOT1 tumors, especially on genes associated with immune response. These interesting results show that the effects of 177Lu-octreotate on tumor tissue needs to be studied further and studies on absorbed dose- and time relationships are ongoing.
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