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Aerosolized BC-819 Inhibits Primary but Not Secondary Lung Cancer Growth

Despite numerous efforts, drug based treatments for patients suffering from lung cancer remains poor. As a promising alternative, we investigated the therapeutic potential of BC-819 for the treatment of lung cancer in mouse tumor models. BC-819 is a novel plasmid DNA which encodes for the A-fragment...

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Autores principales: Hasenpusch, Günther, Pfeifer, Corinna, Aneja, Manish Kumar, Wagner, Kai, Reinhardt, Dietrich, Gilon, Michal, Ohana, Patricia, Hochberg, Avraham, Rudolph, Carsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3110766/
https://www.ncbi.nlm.nih.gov/pubmed/21687669
http://dx.doi.org/10.1371/journal.pone.0020760
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author Hasenpusch, Günther
Pfeifer, Corinna
Aneja, Manish Kumar
Wagner, Kai
Reinhardt, Dietrich
Gilon, Michal
Ohana, Patricia
Hochberg, Avraham
Rudolph, Carsten
author_facet Hasenpusch, Günther
Pfeifer, Corinna
Aneja, Manish Kumar
Wagner, Kai
Reinhardt, Dietrich
Gilon, Michal
Ohana, Patricia
Hochberg, Avraham
Rudolph, Carsten
author_sort Hasenpusch, Günther
collection PubMed
description Despite numerous efforts, drug based treatments for patients suffering from lung cancer remains poor. As a promising alternative, we investigated the therapeutic potential of BC-819 for the treatment of lung cancer in mouse tumor models. BC-819 is a novel plasmid DNA which encodes for the A-fragment of Diphtheria toxin and has previously been shown to successfully inhibit tumor growth in human clinical study of bladder carcinoma. In a first set of experiments, we examined in vitro efficacy of BC-819 in human lung cancer cell-lines NCI-H460, NCI-H358 and A549, which revealed >90% reduction of cell growth. In vivo efficacy was examined in an orthotopic mouse xenograft lung cancer model and in a lung metastasis model using luminescent A549-C8-luc adenocarcinoma cells. These cells resulted in peri- and intra-bronchiolar tumors upon intrabronchial application and parenchymal tumors upon intravenous injection, respectively. Mice suffering from these lung tumors were treated with BC-819, complexed to branched polyethylenimine (PEI) and aerosolized to the mice once per week for a period of 10 weeks. Using this regimen, growth of intrabronchially induced lung tumors was significantly inhibited (p = 0.01), whereas no effect could be observed in mice suffering from lung metastasis. In summary, we suggest that aerosolized PEI/BC-819 is capable of reducing growth only in tumors arising from the luminal part of the airways and are therefore directly accessible for inhaled BC-819.
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spelling pubmed-31107662011-06-16 Aerosolized BC-819 Inhibits Primary but Not Secondary Lung Cancer Growth Hasenpusch, Günther Pfeifer, Corinna Aneja, Manish Kumar Wagner, Kai Reinhardt, Dietrich Gilon, Michal Ohana, Patricia Hochberg, Avraham Rudolph, Carsten PLoS One Research Article Despite numerous efforts, drug based treatments for patients suffering from lung cancer remains poor. As a promising alternative, we investigated the therapeutic potential of BC-819 for the treatment of lung cancer in mouse tumor models. BC-819 is a novel plasmid DNA which encodes for the A-fragment of Diphtheria toxin and has previously been shown to successfully inhibit tumor growth in human clinical study of bladder carcinoma. In a first set of experiments, we examined in vitro efficacy of BC-819 in human lung cancer cell-lines NCI-H460, NCI-H358 and A549, which revealed >90% reduction of cell growth. In vivo efficacy was examined in an orthotopic mouse xenograft lung cancer model and in a lung metastasis model using luminescent A549-C8-luc adenocarcinoma cells. These cells resulted in peri- and intra-bronchiolar tumors upon intrabronchial application and parenchymal tumors upon intravenous injection, respectively. Mice suffering from these lung tumors were treated with BC-819, complexed to branched polyethylenimine (PEI) and aerosolized to the mice once per week for a period of 10 weeks. Using this regimen, growth of intrabronchially induced lung tumors was significantly inhibited (p = 0.01), whereas no effect could be observed in mice suffering from lung metastasis. In summary, we suggest that aerosolized PEI/BC-819 is capable of reducing growth only in tumors arising from the luminal part of the airways and are therefore directly accessible for inhaled BC-819. Public Library of Science 2011-06-08 /pmc/articles/PMC3110766/ /pubmed/21687669 http://dx.doi.org/10.1371/journal.pone.0020760 Text en Hasenpusch et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Hasenpusch, Günther
Pfeifer, Corinna
Aneja, Manish Kumar
Wagner, Kai
Reinhardt, Dietrich
Gilon, Michal
Ohana, Patricia
Hochberg, Avraham
Rudolph, Carsten
Aerosolized BC-819 Inhibits Primary but Not Secondary Lung Cancer Growth
title Aerosolized BC-819 Inhibits Primary but Not Secondary Lung Cancer Growth
title_full Aerosolized BC-819 Inhibits Primary but Not Secondary Lung Cancer Growth
title_fullStr Aerosolized BC-819 Inhibits Primary but Not Secondary Lung Cancer Growth
title_full_unstemmed Aerosolized BC-819 Inhibits Primary but Not Secondary Lung Cancer Growth
title_short Aerosolized BC-819 Inhibits Primary but Not Secondary Lung Cancer Growth
title_sort aerosolized bc-819 inhibits primary but not secondary lung cancer growth
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3110766/
https://www.ncbi.nlm.nih.gov/pubmed/21687669
http://dx.doi.org/10.1371/journal.pone.0020760
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