Inhibition of human lung cancer growth following adenovirus-mediated mda-7 gene expression in vivo

被引:0
|
作者
Tomoyuki Saeki
Abner Mhashilkar
Xin Swanson
X Helena Zou-Yang
Kerry Sieger
Shinichiro Kawabe
Cynthia D Branch
Louis Zumstein
Raymond E Meyn
Jack A Roth
Sunil Chada
Rajagopal Ramesh
机构
[1] Section of Thoracic Molecular Oncology,Department of Thoracic and Cardiovascular Surgery
[2] The University of Texas MD Anderson Cancer Center,Department of Experimental Radiation Oncology
[3] The University of Texas MD Anderson Cancer Center,undefined
[4] Introgen Therapeutics Inc.,undefined
来源
Oncogene | 2002年 / 21卷
关键词
MDA-7; TRAIL; CD31; apoptosis; gene therapy; antiangiogenesis;
D O I
暂无
中图分类号
学科分类号
摘要
Overexpression of the melanoma differentiation associated gene-7 (mda-7) in vitro results in suppression of lung cancer cell proliferation. However, the ability of MDA-7 to suppress lung cancer in vivo has not been previously demonstrated. In this study, we investigated the possibility of inducing overexpression of the mda-7 gene in human non-small cell lung carcinoma cells in vivo and its effects on tumor growth. Adenovirus-mediated overexpression of MDA-7 in p53-wild-type A549 and p53-null H1299 subcutaneous tumors resulted in significant tumor growth inhibition through induction of apoptosis. In addition, decreased CD31/PECAM expression and upregulation of APO2/TRAIL were observed in tumors expressing MDA-7. In vivo studies correlated well with in vitro inhibition of lung tumor cell proliferation and endothelial cell differentiation mediated by Ad-mda7. These data demonstrate that Ad-mda7 functions as a multi-modality anti-cancer agent, possessing both, pro-apoptotic and anti-angiogenic properties. We demonstrate for the first time the potential therapeutic effects of Ad-mda7 in human lung cancer.
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页码:4558 / 4566
页数:8
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