Advances in preclinical investigation of prostate cancer gene therapy

被引:20
作者
Figueiredo, Marxa L.
Kao, Chinghai
Wu, Lily
机构
[1] Univ Calif Los Angeles, Dept Urol, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Mol & Med Pharmacol, Los Angeles, CA USA
[3] Indiana Univ, Sch Med, Dept Urol, Indianapolis, IN USA
关键词
REPLICATION-COMPETENT ADENOVIRUS; VIRUS THYMIDINE KINASE; DOUBLE-SUICIDE GENE; POSITRON-EMISSION-TOMOGRAPHY; SODIUM-IODIDE SYMPORTER; TRANSCRIPTIONAL REGULATORY SEQUENCES; MEMBRANE ANTIGEN PROMOTER/ENHANCER; WILD-TYPE ADENOVIRUS; TRANSGENE EXPRESSION; PHASE-I;
D O I
10.1038/sj.mt.6300181
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
Treating recurrent prostate cancer poses a great challenge to clinicians. Research efforts in the last decade have shown that adenoviral vector-based gene therapy is a promising approach that could expand the arsenal against prostate cancer. This maturing field is at the stage of being able to translate many preclinical discoveries into clinical practices. At this juncture, it is important to highlight the promising strategies including prostate-targeted gene expression, the use of oncolytic vectors, therapy coupled to reporter gene imaging, and combined treatment modalities. In fact, the early stages of clinical investigation employing combined, multimodal gene therapy focused on loco-regional tumor eradication and showed promising results. Clinicians and scientists should seize the momentum of progress to push forward to improve the therapeutic outcome for the patients.
引用
收藏
页码:1053 / 1064
页数:12
相关论文
共 148 条
[11]   A novel TARP-promoter-based adenovirus against hormone-dependent and hormone-refractory prostate cancer [J].
Cheng, WS ;
Kraaij, R ;
Nilsson, B ;
van der Weel, L ;
de Ridder, CMA ;
Tötterman, TH ;
Essand, M .
MOLECULAR THERAPY, 2004, 10 (02) :355-364
[12]   In vivo imaging and radioiodine therapy following sodium iodide symporter gene transfer in animal model of intracerebral gliomas [J].
Cho, JY ;
Shen, DHY ;
Yang, W ;
Williams, B ;
Buckwalter, T ;
La Perle, KMD ;
Hinkle, G ;
Pozderac, R ;
Kloos, R ;
Nagaraja, H ;
Barth, RF ;
Jhiang, SM .
GENE THERAPY, 2002, 9 (17) :1139-1145
[13]  
Chung JK, 2002, J NUCL MED, V43, P1188
[14]   Molecular insights into prostate cancer progression: The missing link of tumor microenvironment [J].
Chung, LWK ;
Baseman, A ;
Assikis, V ;
Zhau, HE .
JOURNAL OF UROLOGY, 2005, 173 (01) :10-20
[15]  
CHUNG LWK, 1995, CANCER SURV, V23, P33
[16]   Two androgen response regions cooperate in steroid hormone regulated activity of the prostate-specific antigen promoter [J].
Cleutjens, KBJM ;
vanEekelen, CCEM ;
vanderKorput, HAGM ;
Brinkmann, AO ;
Trapman, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (11) :6379-6388
[17]   Cloning and characterization of the thyroid iodide transporter [J].
Dai, G ;
Levy, O ;
Carrasco, N .
NATURE, 1996, 379 (6564) :458-460
[18]  
DeWeese TL, 2001, CANCER RES, V61, P7464
[19]   Oncolytic adenovirus CG7870 in combination with radiation demonstrates synergistic enhancements of antitumor efficacy without loss of specificity [J].
Dilley, J ;
Reddy, S ;
Ko, D ;
Nguyen, N ;
Rojas, G ;
Working, P ;
Yu, DC .
CANCER GENE THERAPY, 2005, 12 (08) :715-722
[20]   Tissue-specific, tumor-selective, replication-competent adenovirus vector for cancer gene therapy [J].
Doronin, K ;
Kuppuswamy, M ;
Toth, K ;
Tollefson, AE ;
Krajcsi, P ;
Krougliak, V ;
Wold, WSM .
JOURNAL OF VIROLOGY, 2001, 75 (07) :3314-3324