Bifidobacterium longum as a delivery system for cancer gene therapy:: Selective localization and growth in hypoxic tumors

被引:178
作者
Yazawa, K
Fujimori, M
Amano, J
Kano, Y
Taniguchi, S
机构
[1] Shinshu Univ, Sch Med, Dept Surg, Angio Aging Res Div,Res Ctr Aging & Adaptat, Matsumoto, Nagano 3908621, Japan
[2] Shinshu Univ, Sch Med, Dept Mol Oncol & Angiol, Angio Aging Res Div,Res Ctr Aging & Adaptat, Matsumoto, Nagano 3908621, Japan
[3] Kyoto Pharmaceut Univ, Dept Mol Genet, Inst Mol & Cellular Biol Pharmaceut Sci, Yamashina Ku, Misasagi, Kyoto, Japan
关键词
Bifidobacterium longum; anaerobic bacteria; vector; cancer gene therapy; tumor targeting; hypoxia;
D O I
10.1038/sj.cgt.7700122
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A fundamental obstacle in gene therapy for cancer is the specific delivery of an anticancer gene product to a solid tumor, and yet no systemic delivery system that specifically targets solid tumors currently exists. A strain of domestic bacteria, Bifidobacterium longum, which is nonpathogenic and anaerobic, selectively localized and proliferated in several types of. mouse solid tumors after systemic application. In this report, we further describe a novel approach to cancer gene therapy in which genetically engineered Bifidobacterium is used as a tumor-specific vector. Similarly to wild-type B. longum, genetically engineered B. longum could be detected in tumor tissue only and was not found in a large survey of normal mouse tissues after intravenous injection. This finding strongly suggests that obligate anaerobic bacteria such as Bifidobacterium can be used as highly specific gene delivery vectors for cancer gene therapy.
引用
收藏
页码:269 / 274
页数:6
相关论文
共 24 条
  • [1] A convenient and reproducible method to genetically transform bacteria of the genus Bifidobacterium
    Argnani, A
    Leer, RJ
    vanLuijk, N
    Pouwels, PH
    [J]. MICROBIOLOGY-UK, 1996, 142 : 109 - 114
  • [2] THE CLASSIFICATION OF LACTOBACILLI BY MEANS OF PHYSIOLOGICAL TESTS
    BRIGGS, M
    [J]. JOURNAL OF GENERAL MICROBIOLOGY, 1953, 9 (02): : 234 - 248
  • [3] CAREY R. W., 1967, EUR J CANCER, V3, P37, DOI 10.1016/0014-2964(67)90060-6
  • [4] Targeting gene expression to hypoxic tumor cells
    Dachs, GU
    Patterson, AV
    Firth, JD
    Ratcliffe, PJ
    Townsend, KMS
    Stratford, IJ
    Harris, AL
    [J]. NATURE MEDICINE, 1997, 3 (05) : 515 - 520
  • [5] DRASAR BS, 1969, GASTROENTEROLOGY, V56, P71
  • [6] Fox ME, 1996, GENE THER, V3, P173
  • [7] GORBACH SL, 1967, GASTROENTEROLOGY, V53, P856
  • [8] EVALUATION IN VOLUNTEERS OF A CANDIDATE LIVE ORAL ATTENUATED SALMONELLA-TYPHI VECTOR VACCINE
    HONE, DM
    TACKET, CO
    HARRIS, AM
    KAY, B
    LOSONSKY, G
    LEVINE, MM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (02) : 412 - 420
  • [9] KIMURA NT, 1980, CANCER RES, V40, P2061
  • [10] Anaerobic bacteria as a gene delivery system that is controlled by the tumor microenvironment
    Lemmon, MJ
    vanZijl, P
    Fox, ME
    Mauchline, ML
    Giaccia, AJ
    Minton, NP
    Brown, JM
    [J]. GENE THERAPY, 1997, 4 (08) : 791 - 796