Strategy of Cancer Targeting Gene-Viro-Therapy (CTGVT) a Trend in Both Cancer Gene Therapy and Cancer Virotherapy

被引:11
作者
Liu, Xin-Yuan [1 ,2 ]
Li, Hua-Guang [1 ]
Zhang, Kang-Jian [1 ]
Gu, Jin-Fa [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Biol Sci, Inst Biochem & Cell Biol, Mol Cell Biol Lab, Shanghai 200031, Peoples R China
[2] Zhejiang Sci Tech Univ, Xin Yuan Inst Med & Biotechnol, Coll Life Sci, Hangzhou 310018, Zhejiang, Peoples R China
关键词
Cancer therapy; Cancer targeting; Gene Viro-Therapy; Trend of gene therapy; Trend of virotherapy; DIFFERENTIATION-ASSOCIATED GENE; INCREASES ANTITUMOR-ACTIVITY; ARMED ONCOLYTIC ADENOVIRUS; APOPTOSIS-INDUCING LIGAND; STEM-CELLS; MELANOMA DIFFERENTIATION; COLORECTAL-CANCER; MICE; ANTIBODY; TRAIL;
D O I
10.2174/138920112800958869
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cancer Targeting Gene-Viro-Therapy (CTGVT) and Gene Armed Oncolytic Virus Therapy (GAOVT) both are identical by inserting an antitumor gene into an oncolytic virus. This approach has gradually become a hot topic in cancer therapy, because that CTGVT (GAOVT) has much higher antitumor than that of either gene therapy alone or oncolytic virotherapy alone. We proposed the CTGVT strategy in 1999-2001, insisted it as a long term systematic approach to be examined over 10 years and have published 68 SCI papers some in good Journals. The CD gene armed oncolytic adenovirus therapy (GAOVT) for cancer treatment with potent antitumor effect was also named in our laboratory in 2003. Several modifications to CTGVT will be carried out by our group and will be introduced briefly in this paper. Most importantly, the modifications of CTGVT usually resulted in complete eradication of xenograft tumors in nude mice. In future best antitumor drugs may emerge from the modified CTGVT strategy and not from either gene therapy or virotherapy alone.
引用
收藏
页码:1761 / 1767
页数:7
相关论文
共 34 条
[11]   Stable antibody expression at therapeutic levels using the 2A peptide [J].
Fang, JM ;
Qian, JJ ;
Yi, SL ;
Harding, TC ;
Tu, GH ;
VanRoey, M ;
Jooss, K .
NATURE BIOTECHNOLOGY, 2005, 23 (05) :584-590
[12]   Is mda-7/IL-24 a "magic bullet" for cancer? [J].
Fisher, PB .
CANCER RESEARCH, 2005, 65 (22) :10128-10138
[14]   Examination of the therapeutic potential of Delta-24-RGD in brain tumor stem cells: Role of autophagic, cell death [J].
Jiang, Hong ;
Gomez-Manzano, Candelaria ;
Aoki, Hiroshi ;
Alonso, Marta M. ;
Kondo, Seiji ;
McCormick, Frank ;
Xu, Jing ;
Kondo, Yasuko ;
Bekele, B. Nebiyou ;
Colman, Howard ;
Lang, Frederick F. ;
Fueyo, Juan .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2007, 99 (18) :1410-1414
[15]  
Jiang HP, 1995, ONCOGENE, V11, P2477
[16]   The melanoma differentiation associated gene mda-7 suppresses cancer cell growth [J].
Jiang, HP ;
Su, ZZ ;
Lin, JJ ;
Goldstein, NI ;
Young, CSH ;
Fisher, PB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (17) :9160-9165
[17]   Gene therapy using adenovirus-mediated full-length anti-HER-2 antibody for HER-2 overexpression cancers [J].
Jiang, Minghong ;
Shi, Wenfang ;
Zhang, Qi ;
Wang, Xinhua ;
Guo, Minggao ;
Cui, Zhenfu ;
Su, Changqin ;
Yang, Qing ;
Li, Yuemin ;
Sham, Jonathan ;
Liu, Xinyuan ;
Wu, Mengchao ;
Qian, Qijun .
CLINICAL CANCER RESEARCH, 2006, 12 (20) :6179-6185
[18]   A CELL INITIATING HUMAN ACUTE MYELOID-LEUKEMIA AFTER TRANSPLANTATION INTO SCID MICE [J].
LAPIDOT, T ;
SIRARD, C ;
VORMOOR, J ;
MURDOCH, B ;
HOANG, T ;
CACERESCORTES, J ;
MINDEN, M ;
PATERSON, B ;
CALIGIURI, MA ;
DICK, JE .
NATURE, 1994, 367 (6464) :645-648
[19]  
Liu X.R, J CELLULAR MOL MED
[20]   Effective gene-virotherapy tumor mediated by the for complete eradication of combination of hTRAIL (TNFSF10) and plasminogen k5 [J].
Liu, XY ;
Qiu, SB ;
Zou, WG ;
Pei, ZF ;
Gu, JF ;
Luo, CX ;
Ruan, HM ;
Chen, Y ;
Qi, YP ;
Qian, C .
MOLECULAR THERAPY, 2005, 11 (04) :531-541