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DDMC-p53 gene therapy with or without cisplatin and microwave ablation

Lung cancer remains the leading cause of death in cancer patients. Severe treatment side effects and late stage of disease at diagnosis continue to be an issue. We investigated whether local treatment using 2-diethylaminoethyl-dextran methyl methacrylate copolymer with p53 (DDMC-p53) with or without...

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Autores principales: Hohenforst-Schmidt, Wolfgang, Zarogoulidis, Paul, Stopek, Joshua, Vogl, Thomas, Hübner, Frank, Turner, J Francis, Browning, Robert, Zarogoulidis, Konstantinos, Drevelegas, Antonis, Drevelegas, Konstantinos, Darwiche, Kaid, Freitag, Lutz, Rittger, Harald
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446017/
https://www.ncbi.nlm.nih.gov/pubmed/26056480
http://dx.doi.org/10.2147/OTT.S83794
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author Hohenforst-Schmidt, Wolfgang
Zarogoulidis, Paul
Stopek, Joshua
Vogl, Thomas
Hübner, Frank
Turner, J Francis
Browning, Robert
Zarogoulidis, Konstantinos
Drevelegas, Antonis
Drevelegas, Konstantinos
Darwiche, Kaid
Freitag, Lutz
Rittger, Harald
author_facet Hohenforst-Schmidt, Wolfgang
Zarogoulidis, Paul
Stopek, Joshua
Vogl, Thomas
Hübner, Frank
Turner, J Francis
Browning, Robert
Zarogoulidis, Konstantinos
Drevelegas, Antonis
Drevelegas, Konstantinos
Darwiche, Kaid
Freitag, Lutz
Rittger, Harald
author_sort Hohenforst-Schmidt, Wolfgang
collection PubMed
description Lung cancer remains the leading cause of death in cancer patients. Severe treatment side effects and late stage of disease at diagnosis continue to be an issue. We investigated whether local treatment using 2-diethylaminoethyl-dextran methyl methacrylate copolymer with p53 (DDMC-p53) with or without cisplatin and/or microwave ablation enhances disease control in BALBC mice. We used a Lewis lung carcinoma cell line to inoculate 140 BALBC mice, which were divided into the following seven groups; control, cisplatin, microwave ablation, DDMC-p53, DDMC-p53 plus cisplatin, DDMC-p53 plus microwave, and DDMC-p53 plus cisplatin plus microwave. Microwave ablation energy was administered at 20 W for 10 minutes. Cisplatin was administered as 1 mL/mg and the DDMC-p53 complex delivered was 0.5 mL. Increased toxicity was observed in the group receiving DDMC-p53 plus cisplatin plus microwave followed by the group receiving DDMC-p53 plus cisplatin. Infection after repeated treatment administration was a major issue. We conclude that a combination of gene therapy using DDMC-p53 with or without cisplatin and microwave is an alternative method for local disease control. However, more experiments are required in a larger model to identify the appropriate dosage profile.
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spelling pubmed-44460172015-06-08 DDMC-p53 gene therapy with or without cisplatin and microwave ablation Hohenforst-Schmidt, Wolfgang Zarogoulidis, Paul Stopek, Joshua Vogl, Thomas Hübner, Frank Turner, J Francis Browning, Robert Zarogoulidis, Konstantinos Drevelegas, Antonis Drevelegas, Konstantinos Darwiche, Kaid Freitag, Lutz Rittger, Harald Onco Targets Ther Original Research Lung cancer remains the leading cause of death in cancer patients. Severe treatment side effects and late stage of disease at diagnosis continue to be an issue. We investigated whether local treatment using 2-diethylaminoethyl-dextran methyl methacrylate copolymer with p53 (DDMC-p53) with or without cisplatin and/or microwave ablation enhances disease control in BALBC mice. We used a Lewis lung carcinoma cell line to inoculate 140 BALBC mice, which were divided into the following seven groups; control, cisplatin, microwave ablation, DDMC-p53, DDMC-p53 plus cisplatin, DDMC-p53 plus microwave, and DDMC-p53 plus cisplatin plus microwave. Microwave ablation energy was administered at 20 W for 10 minutes. Cisplatin was administered as 1 mL/mg and the DDMC-p53 complex delivered was 0.5 mL. Increased toxicity was observed in the group receiving DDMC-p53 plus cisplatin plus microwave followed by the group receiving DDMC-p53 plus cisplatin. Infection after repeated treatment administration was a major issue. We conclude that a combination of gene therapy using DDMC-p53 with or without cisplatin and microwave is an alternative method for local disease control. However, more experiments are required in a larger model to identify the appropriate dosage profile. Dove Medical Press 2015-05-20 /pmc/articles/PMC4446017/ /pubmed/26056480 http://dx.doi.org/10.2147/OTT.S83794 Text en © 2015 Hohenforst-Schmidt et al. This work is published by Dove Medical Press Limited, and licensed under Creative Commons Attribution – Non Commercial (unported, v3.0) License The full terms of the License are available at http://creativecommons.org/licenses/by-nc/3.0/. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Hohenforst-Schmidt, Wolfgang
Zarogoulidis, Paul
Stopek, Joshua
Vogl, Thomas
Hübner, Frank
Turner, J Francis
Browning, Robert
Zarogoulidis, Konstantinos
Drevelegas, Antonis
Drevelegas, Konstantinos
Darwiche, Kaid
Freitag, Lutz
Rittger, Harald
DDMC-p53 gene therapy with or without cisplatin and microwave ablation
title DDMC-p53 gene therapy with or without cisplatin and microwave ablation
title_full DDMC-p53 gene therapy with or without cisplatin and microwave ablation
title_fullStr DDMC-p53 gene therapy with or without cisplatin and microwave ablation
title_full_unstemmed DDMC-p53 gene therapy with or without cisplatin and microwave ablation
title_short DDMC-p53 gene therapy with or without cisplatin and microwave ablation
title_sort ddmc-p53 gene therapy with or without cisplatin and microwave ablation
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4446017/
https://www.ncbi.nlm.nih.gov/pubmed/26056480
http://dx.doi.org/10.2147/OTT.S83794
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