Antiangiogenic gene therapy targeting the endothelium-specific receptor tyrosine kinase Tie2

被引:302
作者
Lin, PN
Buxton, JA
Acheson, A
Radziejewski, C
Maisonpierre, PC
Yancopoulos, GD
Channon, KM
Hale, LP
Dewhirst, MW
George, SE
Peters, KG
机构
[1] Duke Univ, Med Ctr, Dept Med, Durham, NC 27710 USA
[2] Duke Univ, Med Ctr, Dept Radiat Oncol, Durham, NC 27710 USA
[3] Duke Univ, Med Ctr, Dept Pharmacol, Durham, NC 27710 USA
[4] Duke Univ, Med Ctr, Dept Pathol, Durham, NC 27710 USA
[5] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
关键词
cancer; adenovirus; soluble receptor; tumor angiogenesis;
D O I
10.1073/pnas.95.15.8829
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Angiogenesis is required for tumor growth and metastasis, and inhibition of angiogenesis is a promising approach for anticancer therapy, Tie2 (a.k.a Tek) is an endothelium-specific receptor tyrosine kinase known to play a role in tumor angiogenesis, To explore the therapeutic potential of blocking the Tie2 pathway, an adenoviral vector was constructed to deliver a recombinant, soluble Tie2 receptor (AdExTek) capable of blocking Tie2 activation. Two days after i.v. injection of AdExTek, the plasma concentration of ExTek exceeded 1 mg/ml and was maintained for about 8 days. Administration of AdExTek to mice with two different well established primary tumors, a murine mammary carcinoma (4T1) or a murine melanoma (B16F10.9), significantly inhibited the growth rate of both tumors (64% and 47%, respectively), To study the effect of ExTek on tumor metastasis, both tumor cell lines were coinjected i.v. with either AdExTek or a control virus. Mice coinjected with control virus developed numerous large, well vascularized lung metastases, In contrast, mice coinjected with AdExTek virus developed few, if any, grossly apparent metastases, and histologic examination revealed only small avascular clusters of tumor cells, Administration of AdExTek also inhibited tumor metastasis when delivered at the time of surgical excision of primary tumors in a clinically relevant model of tumor metastasis. This study demonstrates the potential utility of gene therapy for systemic delivery of an antiangiogenic agent targeting an endothelium-specific receptor, Tie2.
引用
收藏
页码:8829 / 8834
页数:6
相关论文
共 42 条
[31]   Adeno-associated virus-mediated gene transfer into rat carotid arteries [J].
Rolling, F ;
Nong, Z ;
Pisvin, S ;
Collen, D .
GENE THERAPY, 1997, 4 (08) :757-761
[32]   DISTINCT ROLES OF THE RECEPTOR TYROSINE KINASES TIE-1 AND TIE-2 IN BLOOD-VESSEL FORMATION [J].
SATO, TN ;
TOZAWA, Y ;
DEUTSCH, U ;
WOLBURGBUCHHOLZ, K ;
FUJIWARA, Y ;
GENDRONMAGUIRE, M ;
GRIDLEY, T ;
WOLBURG, H ;
RISAU, W ;
QIN, Y .
NATURE, 1995, 376 (6535) :70-74
[33]  
SCHNURCH H, 1993, DEVELOPMENT, V119, P957
[34]   Persistent and therapeutic concentrations of human factor IX in mice after hepatic gene transfer of recombinant AAV vectors [J].
Snyder, RO ;
Miao, CH ;
Patijn, GA ;
Spratt, SK ;
Danos, O ;
Nagy, D ;
Gown, AM ;
Winther, B ;
Meuse, L ;
Cohen, LK ;
Thompson, AR ;
Kay, MA .
NATURE GENETICS, 1997, 16 (03) :270-276
[35]   TUMOR ANGIOGENESIS IS AN INDEPENDENT PROGNOSTIC INDICATOR IN PRIMARY BREAST-CARCINOMA [J].
TOI, M ;
KASHITANI, J ;
TOMINAGA, T .
INTERNATIONAL JOURNAL OF CANCER, 1993, 55 (03) :371-374
[36]   INDUCTION OF ANTITUMOR IMMUNITY BY INTERLEUKIN-2 GENE-TRANSDUCED MOUSE MAMMARY-TUMOR CELLS VERSUS TRANSDUCED MAMMARY STROMAL FIBROBLASTS [J].
TSAI, SCJ ;
GANSBACHER, B ;
TAIT, L ;
MILLER, FR ;
HEPPNER, GH .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (07) :546-553
[37]   Gene therapy - promises, problems and prospects [J].
Verma, IM ;
Somia, N .
NATURE, 1997, 389 (6648) :239-242
[38]   TUMOR ANGIOGENESIS - A NEW SIGNIFICANT AND INDEPENDENT PROGNOSTIC INDICATOR IN EARLY-STAGE BREAST-CARCINOMA [J].
WEIDNER, N ;
FOLKMAN, J ;
POZZA, F ;
BEVILACQUA, P ;
ALLRED, EN ;
MOORE, DH ;
MELI, S ;
GASPARINI, G .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1992, 84 (24) :1875-1887
[39]   TUMOR ANGIOGENESIS AND METASTASIS - CORRELATION IN INVASIVE BREAST-CARCINOMA [J].
WEIDNER, N ;
SEMPLE, JP ;
WELCH, WR ;
FOLKMAN, J .
NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (01) :1-8
[40]  
WEIDNER N, 1993, AM J PATHOL, V143, P401