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Cancer Targeted Gene Therapy of BikDD Inhibits Orthotopic Lung Cancer Growth and Improves Long-term Survival
Lung cancer is a leading cause of cancer death due to the high incidence of metastasis; therefore novel and effective treatments are urgently needed. A current strategy is cancer specific targeted gene therapy. While many identified cancer specific promoters are highly specific, they tend to have lo...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2763377/ https://www.ncbi.nlm.nih.gov/pubmed/19597463 http://dx.doi.org/10.1038/onc.2009.187 |
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author | Sher, Yuh-Pyng Tzeng, Tz-Fei Kan, Shu-Fen Hsu, Jennifer Xie, Xiaoming Han, Zhenbo Lin, Wen-Chuan Li, Long-Yuan Hung, Mien-Chie |
author_facet | Sher, Yuh-Pyng Tzeng, Tz-Fei Kan, Shu-Fen Hsu, Jennifer Xie, Xiaoming Han, Zhenbo Lin, Wen-Chuan Li, Long-Yuan Hung, Mien-Chie |
author_sort | Sher, Yuh-Pyng |
collection | PubMed |
description | Lung cancer is a leading cause of cancer death due to the high incidence of metastasis; therefore novel and effective treatments are urgently needed. A current strategy is cancer specific targeted gene therapy. While many identified cancer specific promoters are highly specific, they tend to have low activity compared to the ubiquitous CMV promoter, limiting their application. We developed a targeted gene therapy expression system for lung cancer that is highly specific with strong activity. Our expression vector uses the survivin promoter, highly expressed in many cancers but not normal adult tissues. We enhanced the survivin promoter activity comparable to the CMV promoter in lung cancer cell lines using an established platform technology, while the survivin promoter remained weak in normal cells. In mouse models, the transgene was specifically expressed in the lung tumor tissue, compared with the CMV promoter that was expressed in both normal and tumor tissues. Additionally, the therapeutic gene BikDD, a mutant form of pro-apoptotic Bik, induced cell killing in vitro, and inhibited cell growth and prolonged mouse survival in vivo. Importantly, there was virtually no toxicity when BikDD was expressed with our expression system. Thus, the current report provides a therapeutic efficacy and safe strategy worthy of development in clinical trials treating lung cancer. |
format | Text |
id | pubmed-2763377 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
record_format | MEDLINE/PubMed |
spelling | pubmed-27633772010-03-17 Cancer Targeted Gene Therapy of BikDD Inhibits Orthotopic Lung Cancer Growth and Improves Long-term Survival Sher, Yuh-Pyng Tzeng, Tz-Fei Kan, Shu-Fen Hsu, Jennifer Xie, Xiaoming Han, Zhenbo Lin, Wen-Chuan Li, Long-Yuan Hung, Mien-Chie Oncogene Article Lung cancer is a leading cause of cancer death due to the high incidence of metastasis; therefore novel and effective treatments are urgently needed. A current strategy is cancer specific targeted gene therapy. While many identified cancer specific promoters are highly specific, they tend to have low activity compared to the ubiquitous CMV promoter, limiting their application. We developed a targeted gene therapy expression system for lung cancer that is highly specific with strong activity. Our expression vector uses the survivin promoter, highly expressed in many cancers but not normal adult tissues. We enhanced the survivin promoter activity comparable to the CMV promoter in lung cancer cell lines using an established platform technology, while the survivin promoter remained weak in normal cells. In mouse models, the transgene was specifically expressed in the lung tumor tissue, compared with the CMV promoter that was expressed in both normal and tumor tissues. Additionally, the therapeutic gene BikDD, a mutant form of pro-apoptotic Bik, induced cell killing in vitro, and inhibited cell growth and prolonged mouse survival in vivo. Importantly, there was virtually no toxicity when BikDD was expressed with our expression system. Thus, the current report provides a therapeutic efficacy and safe strategy worthy of development in clinical trials treating lung cancer. 2009-07-13 2009-09-17 /pmc/articles/PMC2763377/ /pubmed/19597463 http://dx.doi.org/10.1038/onc.2009.187 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Sher, Yuh-Pyng Tzeng, Tz-Fei Kan, Shu-Fen Hsu, Jennifer Xie, Xiaoming Han, Zhenbo Lin, Wen-Chuan Li, Long-Yuan Hung, Mien-Chie Cancer Targeted Gene Therapy of BikDD Inhibits Orthotopic Lung Cancer Growth and Improves Long-term Survival |
title | Cancer Targeted Gene Therapy of BikDD Inhibits Orthotopic Lung Cancer Growth and Improves Long-term Survival |
title_full | Cancer Targeted Gene Therapy of BikDD Inhibits Orthotopic Lung Cancer Growth and Improves Long-term Survival |
title_fullStr | Cancer Targeted Gene Therapy of BikDD Inhibits Orthotopic Lung Cancer Growth and Improves Long-term Survival |
title_full_unstemmed | Cancer Targeted Gene Therapy of BikDD Inhibits Orthotopic Lung Cancer Growth and Improves Long-term Survival |
title_short | Cancer Targeted Gene Therapy of BikDD Inhibits Orthotopic Lung Cancer Growth and Improves Long-term Survival |
title_sort | cancer targeted gene therapy of bikdd inhibits orthotopic lung cancer growth and improves long-term survival |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2763377/ https://www.ncbi.nlm.nih.gov/pubmed/19597463 http://dx.doi.org/10.1038/onc.2009.187 |
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