Recombinant adenovirus encoding vasohibin prevents tumor angiogenesis and inhibits tumor growth

被引:29
作者
Li, Dajiang [2 ]
Zhou, Kun [1 ]
Wang, Shuguang [2 ]
Shi, Zhong [1 ]
Yang, Zhao [1 ]
机构
[1] Third Mil Med Univ, Xinqiao Hosp, Dept Emergency, Chongqing, Peoples R China
[2] Third Mil Med Univ, SW Hosp, Inst Hepatobiliary Surg, Chongqing, Peoples R China
关键词
NEGATIVE FEEDBACK REGULATOR; COLORECTAL-CANCER; BLOOD-VESSELS; CELLS; TARGET; STRATEGY; VASCULATURE; THERAPY; THROMBOSPONDIN-1; ENDOTHELIUM;
D O I
10.1111/j.1349-7006.2009.01388.x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Numerous lines of evidence have shown that angiogenesis plays a pivotal role in the development of tumors. Therefore anti-angiogenesis therapy represents a potentially promising approach to cancer therapy. Recently, a new inhibitor called vasohibin was discovered to operate as an intrinsic and highly specific feedback inhibitor in the process of angiogenesis. However, to date, reports on the antitumor and anti-angiogenic properties of vasohibin have been very limited. To explore the potential of vasohibin as an anti-angiogenesis therapeutic, we constructed a recombinant adenovirus encoding vasohibin. Our data showed that the recombinant adenovirus encoding vasohibin could prevent tumor angiogenesis and tumor growth. Notably, angiogenesis in the tumors was prevented without any apparent side-effects. Therefore, the findings suggested that the recombinant adenovirus encoding vasohibin might be valuable as a potential strategy for antitumor angiogenesis therapy in the clinic. (Cancer Sci 2010; 101: 448-452)
引用
收藏
页码:448 / 452
页数:5
相关论文
共 34 条
[1]   Bystander cell killing spreading from endothelial to tumor cells in a three-dimensional multicellular nodule model after Escherichia coli nitroreductase gene delivery [J].
Benouchan, M ;
Do Nascimento, F ;
Sebbah-Louriki, M ;
Salzmann, JL ;
Crépin, M ;
Perret, GY ;
Colombo, BM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 311 (04) :822-828
[2]  
Casas A, 2006, INT J ONCOL, V29, P397
[3]   CONTROL OF ANGIOGENESIS IN FIBROBLASTS BY P53 REGULATION OF THROMBOSPONDIN-1 [J].
DAMERON, KM ;
VOLPERT, OV ;
TAINSKY, MA ;
BOUCK, N .
SCIENCE, 1994, 265 (5178) :1582-1584
[4]   Microsatellite instability in tumor and nonneoplastic colorectal cells from hereditary non-polyposis colorectal cancer and sporadic high microsatellite-instable tumor patients [J].
Dietmaier, W ;
Gänsbauer, S ;
Beyser, K ;
Renke, B ;
Hartmann, A ;
Rümmele, P ;
Jauch, KW ;
Hofstädter, F ;
Rüschoff, J .
PATHOBIOLOGY, 2000, 68 (4-5) :227-231
[5]   Pigment epithelium-derived factor regulates the vasculature and mass of the prostate and pancreas [J].
Doll, JA ;
Stellmach, VM ;
Bouck, NP ;
Bergh, ARJ ;
Lee, C ;
Abramson, LP ;
Cornwell, ML ;
Pins, MR ;
Borensztajn, J ;
Crawford, SE .
NATURE MEDICINE, 2003, 9 (06) :774-780
[6]  
Dome Balazs, 2008, Magy Onkol, V52, P247, DOI 10.1556/MOnkol.52.2008.3.2
[7]  
Eberhard A, 2000, CANCER RES, V60, P1388
[8]   VEGF and the quest for tumour angiogenesis factors [J].
Ferrara, N .
NATURE REVIEWS CANCER, 2002, 2 (10) :795-803
[9]   Discovery and development of bevacizumab, an anti-VEGF antibody for treating cancer [J].
Ferrara, N ;
Hillan, KJ ;
Gerber, HP ;
Novotny, W .
NATURE REVIEWS DRUG DISCOVERY, 2004, 3 (05) :391-400
[10]   Role of angiogenesis in tumor growth and metastasis [J].
Folkman, J .
SEMINARS IN ONCOLOGY, 2002, 29 (06) :15-18