Literature DB >> 8509217

Biodistribution study of 99mTc-labeled LDL in B16-melanoma-bearing mice. Visualization of a preferential uptake by the tumor.

E Ponty1, G Favre, R Benaniba, A Boneu, H Lucot, M Carton, G Soula.   

Abstract

Since there is strong evidence of a preferential LDL accumulation in tumor cells, LDL might be of interest for tumor imaging. We have tested the ability of 99mTc-LDL in tumor imaging with B16-melanoma-bearing mice as a model for further applications in human studies. The LDL fixation rate was higher with 99mTc-labeled LDL than with 125I labeled LDL. Since technetium-99m remains trapped in the cells, 99mTc-LDL is a well-adapted radioligand because of information given by this radiotracer on the receptor metabolism. We observed that, at early growth stages, the tumor took up the LDL at a maximal rate, suggesting differences in cholesterol metabolism as a function of tumor growth. Accumulation of label in the tumor area was perfectly observable in tumor-bearing mice on scintigraphic images. Computerized quantification of the regions of interest (as well as biodistribution studies including killing of the animals) showed a 1.81-fold increase in uptake by the tumor as compared to the liver and a 28-fold increase as compared with corresponding normal tissue (muscle of the left leg) at day 8 of tumor growth. These data give strong support to the value of this non-invasive method in visualizing and quantifying the tissue LDL uptake in vivo, including the precise information provided by nuclear scintigraphy on the distribution of the radiolabeled LDL in the different tissues. 99mTc-LDL could be an efficient tool for further diagnostic or therapeutic exploration in cancer patients.

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Year:  1993        PMID: 8509217     DOI: 10.1002/ijc.2910540311

Source DB:  PubMed          Journal:  Int J Cancer        ISSN: 0020-7136            Impact factor:   7.396


  8 in total

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Authors:  Jean-Pierre Daziano; Wolfgang H H Günther; Marianne Krieg; Ichiro Tsujino; Kiyoko Miyagi; Gregory S Anderson; Reynée W Sampson; Martin D Ostrowski; Sarah A Muir; Raymond J Bula; Fritz Sieber
Journal:  Photochem Photobiol       Date:  2012-01-31       Impact factor: 3.421

2.  Low-density lipoprotein nanoparticles as magnetic resonance imaging contrast agents.

Authors:  Ian R Corbin; Hui Li; Juan Chen; Sissel Lund-Katz; Rong Zhou; Jerry D Glickson; Gang Zheng
Journal:  Neoplasia       Date:  2006-06       Impact factor: 5.715

3.  Selective uptake of boronated low-density lipoprotein in melanoma xenografts achieved by diet supplementation.

Authors:  Y Setiawan; D E Moore; B J Allen
Journal:  Br J Cancer       Date:  1996-12       Impact factor: 7.640

4.  ELEMENTAL SELENIUM GENERATED BY THE PHOTOBLEACHING OF SELENOMEROCYANINE PHOTOSENSITIZERS FORMS CONJUGATES WITH SERUM MACROMOLECULES THAT ARE TOXIC TO TUMOR CELLS.

Authors:  Fritz Sieber; Jean-Pierre Daziano; Wolfgang H H Günther; Marianne Krieg; Kiyoko Miyagi; Reynée W Sampson; Martin D Ostrowski; Gregory S Anderson; Ichiro Tsujino; Raymond J Bula
Journal:  Phosphorus Sulfur Silicon Relat Elem       Date:  2005

Review 5.  Lipoprotein-inspired nanoparticles for cancer theranostics.

Authors:  Kenneth K Ng; Jonathan F Lovell; Gang Zheng
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6.  Receptor-mediated uptake of low-density lipoprotein by B16 melanoma cells in vitro and in vivo in mice.

Authors:  A J Versluis; P J van Geel; H Oppelaar; T J van Berkel; M K Bijsterbosch
Journal:  Br J Cancer       Date:  1996-08       Impact factor: 7.640

7.  Low-density lipoprotein receptor-mediated delivery of a lipophilic daunorubicin derivative to B16 tumours in mice using apolipoprotein E-enriched liposomes.

Authors:  A J Versluis; P C Rensen; E T Rump; T J Van Berkel; M K Bijsterbosch
Journal:  Br J Cancer       Date:  1998-12       Impact factor: 7.640

Review 8.  Lipoprotein-Related and Apolipoprotein-Mediated Delivery Systems for Drug Targeting and Imaging.

Authors:  Gunter Almer; Harald Mangge; Andreas Zimmer; Ruth Prassl
Journal:  Curr Med Chem       Date:  2015       Impact factor: 4.530

  8 in total

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