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Erschienen in: Journal of Cancer Research and Clinical Oncology 9/2009

01.09.2009 | Original Paper

Therapeutic effects of recombinant human endostatin adenovirus in a mouse model of malignant pleural effusion

verfasst von: Fang Fang, Ping Chen, Xin Wu, Li Yang, Xun Yang, Zhen-Xiang Xi, Bin-Wen Zhou, Xi-Kun Zhou, Zhi-Yong Qian, Bo Xiao, Yu-Quan Wei

Erschienen in: Journal of Cancer Research and Clinical Oncology | Ausgabe 9/2009

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Abstract

Purpose

Malignant pleural effusion (MPE) is a common clinical problem in patients with advanced cancer. Evidence suggests that tumor-mediated angiogenesis and enhanced vascular permeability in the pleural wall are due to high levels of vascular endothelial growth factor (VEGF), which plays an important role in the pathogenesis of MPE. The present study was designed to test whether the recombinant adenovirus-mediated delivery of human endostatin (Ad-hEndo), one of the potent inhibitors of angiogenesis, would inhibit the formation and progression of MPE.

Methods

We developed a novel mouse model of MPE by injecting Lewis lung carcinoma (LLC) cells directly into pleural cavity of C57BL/6 mice. To evaluate the therapeutic effects of endostatin in this MPE model, we injected the Ad-hEndo into the pleural cavity of MPE-bearing mice three times with the 3-day interval.

Results

We found that this treatment resulted in significant reduction in pleural effusion volume, the number of pleural tumor foci, microvessel density, and vascular permeability, while it significantly prolonged the survival time. In addition, VEGF level of MPE in the group administered with the Ad-hEndo was obviously decreased as compared with that in the two control groups administered with null-adenovirus (Ad-null) or normal saline.

Conclusions

Our work provides a rationale for future studies toward evaluating the effectiveness of the adenovirus-based endostatin therapy for MPE.
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Metadaten
Titel
Therapeutic effects of recombinant human endostatin adenovirus in a mouse model of malignant pleural effusion
verfasst von
Fang Fang
Ping Chen
Xin Wu
Li Yang
Xun Yang
Zhen-Xiang Xi
Bin-Wen Zhou
Xi-Kun Zhou
Zhi-Yong Qian
Bo Xiao
Yu-Quan Wei
Publikationsdatum
01.09.2009
Verlag
Springer-Verlag
Erschienen in
Journal of Cancer Research and Clinical Oncology / Ausgabe 9/2009
Print ISSN: 0171-5216
Elektronische ISSN: 1432-1335
DOI
https://doi.org/10.1007/s00432-009-0555-y

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