Combined effects of radiotherapy and angiostatin gene therapy in glioma tumor model

被引:103
作者
Griscelli, F
Li, H
Cheong, C
Opolon, P
Bennaceur-Griscelli, A
Vassal, G
Soria, J
Soria, C
Lu, H
Perricaudet, M
Yeh, P
机构
[1] Inst Gustave Roussy, CNRS, UMR 1582, Rhone Poulenc Gencell, F-94805 Villejuif, France
[2] Inst Gustave Roussy, Lab Hematol Biol, F-94805 Villejuif, France
[3] Inst Gustave Roussy, UMR 8532, F-94805 Villejuif, France
[4] Hotel Dieu, Biochim Lab, F-75004 Paris, France
[5] Fac Med, DIFEMA, F-76000 Rouen, France
[6] Hop St Louis, INSERM, U353, F-75010 Paris, France
关键词
angiogenesis; recombinant adenovirus; cancer;
D O I
10.1073/pnas.110134297
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
The objective of the present study was to evaluate the antitumor effect of a defective adenovirus expressing a secretable angiostatin-like molecule (AdK3) in combination with radiotherapy in rat C6 gliomas s.c. preestablished into athymic mice. In vitro, the combination regimen was significantly (P < 0.001) more cytotoxic for human microcapillary endothelial cells than either treatment alone, whereas survival of C6 glioma cells was not affected in the conditions used. Radiotherapy and AdK3 gene delivery was then studied on well established C6 xenografts (165 +/- 70 mm(3)). In these tumors, AdK3 intratumoral injections had only a marginal effect. Interestingly, when experimental radiotherapy was added, significantly higher (P < 0.005), and possibly synergistic, antitumoral effects were observed that tightly correlated a marked decrease of intratumoral vascularization. The combination of radiotherapy and AdK3 intratumoral injections also revealed a significant (P < 0.05) inhibition of tumor growth as compared with either treatment alone for larger tumors (467 +/- 120 mm(3)). Altogether, these data emphasize the potential of combining a destructive strategy directed against the tumor cells with an anti-angiogenic approach to fight cancer.
引用
收藏
页码:6698 / 6703
页数:6
相关论文
共 30 条
  • [1] Effects of angiogenesis inhibitors on multistage carcinogenesis in mice
    Bergers, G
    Javaherian, K
    Lo, KM
    Folkman, J
    Hanahan, D
    [J]. SCIENCE, 1999, 284 (5415) : 808 - 812
  • [2] BRAIN-TUMORS .2.
    BLACK, PM
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1991, 324 (22) : 1555 - 1564
  • [3] BRANDES A, 1991, ANTICANCER RES, V11, P719
  • [4] THE CURRENT STATUS OF TARGETING TUMOR VASCULATURE AS A MEANS OF CANCER-THERAPY - AN OVERVIEW
    DENEKAMP, J
    [J]. INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1991, 60 (1-2) : 401 - 408
  • [5] CHARACTERISTICS OF A HUMAN CELL LINE TRANSFORMED BY DNA FROM HUMAN ADENOVIRUS TYPE-5
    GRAHAM, FL
    SMILEY, J
    RUSSELL, WC
    NAIRN, R
    [J]. JOURNAL OF GENERAL VIROLOGY, 1977, 36 (JUL) : 59 - 72
  • [6] Gridley DS, 1998, INT J ONCOL, V13, P1093
  • [7] Angiostatin gene transfer:: Inhibition of tumor growth in vivo by blockage of endothelial cell proliferation associated with a mitosis arrest
    Griscelli, F
    Li, H
    Bennaceur-Griscelli, A
    Soria, J
    Opolon, P
    Soria, C
    Perricaudet, M
    Yeh, P
    Lu, H
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (11) : 6367 - 6372
  • [8] Patterns and emerging mechanisms of the angiogenic switch during tumorigenesis
    Hanahan, D
    Folkman, J
    [J]. CELL, 1996, 86 (03) : 353 - 364
  • [9] In vivo experimental evidence that the nitric oxide pathway is involved in the X-ray-induced antiangiogenicity
    Hatjikondi, O
    Ravazoula, P
    Kardamakis, D
    Dimopoulos, J
    Papaioannou, S
    [J]. BRITISH JOURNAL OF CANCER, 1996, 74 (12) : 1916 - 1923
  • [10] TUMOR MICROVASCULATURE FOLLOWING FRACTIONATED X-IRRADIATION
    HILMAS, DE
    GILLETTE, EL
    [J]. RADIOLOGY, 1975, 116 (01) : 165 - 169