Replication-selective oncolytic viruses in the treatment of cancer

被引:132
作者
Everts, B
van der Poel, HG
机构
[1] Netherlands Canc Inst, Dept Urol, NL-1066 CX Amsterdam, Netherlands
[2] Univ Amsterdam, Dept Biomed Sci, NL-1098 SM Amsterdam, Netherlands
关键词
oncolysis; tumors; replication competent virus; clinical trials;
D O I
10.1038/sj.cgt.7700771
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
In the search for novel strategies, oncolytic virotherapy has recently emerged as a viable approach to specifically kill tumor cells. Unlike conventional gene therapy, it uses replication competent viruses that are able to spread through tumor tissue by virtue of viral replication and concomitant cell lysis. Recent advances in molecular biology have allowed the design of several genetically modified viruses, such as adenovirus and herpes simplex virus that specifically replicate in, and kill tumor cells. On the other hand, viruses with intrinsic oncolytic capacity are also being evaluated for therapeutic purposes. In this review, an overview is given of the general mechanisms and genetic modifications by which these viruses achieve tumor cell-specific replication and antitumor efficacy. However, although generally the oncolytic efficacy of these approaches has been demonstrated in preclinical studies the therapeutic efficacy in clinical trails is still not optimal. Therefore, strategies are evaluated that could further enhance the oncolytic potential of conditionally replicating viruses. In this respect, the use of tumor-selective viruses in conjunction with other standard therapies seems most promising. However, still several hurdles regarding clinical limitations and safety issues should be overcome before this mode of therapy can become of clinical relevance.
引用
收藏
页码:141 / 161
页数:21
相关论文
共 172 条
[1]  
Adachi Y, 2001, CANCER RES, V61, P7882
[2]   Enhancement of replication of genetically engineered herpes simplex viruses by ionizing radiation: a new paradigm for destruction of therapeutically intractable tumors [J].
Advani, SJ ;
Sibley, GS ;
Song, PY ;
Hallahan, DE ;
Kataoka, Y ;
Roizman, B ;
Weichselbaum, RR .
GENE THERAPY, 1998, 5 (02) :160-165
[3]  
Aghi M, 1999, CANCER RES, V59, P3861
[4]   Reovirus therapy of lymphoid malignancies [J].
Alain, T ;
Hirasawa, K ;
Pon, KJ ;
Nishikawa, SG ;
Urbanski, SJ ;
Auer, Y ;
Luider, J ;
Martin, A ;
Johnston, RN ;
Janowska-Wieczorek, A ;
Lee, PWK ;
Kossakowska, AE .
BLOOD, 2002, 100 (12) :4146-4153
[5]   Treatment of intracranial gliomas in immunocompetent mice using herpes simplex viruses that express murine interleukins [J].
Andreansky, S ;
He, B ;
van Cott, J ;
McGhee, J ;
Markert, JM ;
Gillespie, GY ;
Roizman, B ;
Whitley, RJ .
GENE THERAPY, 1998, 5 (01) :121-130
[6]  
[Anonymous], INT J CANCER, DOI DOI 10.1038/nrc1750
[7]  
ASADA T, 1974, CANCER, V34, P1907, DOI 10.1002/1097-0142(197412)34:6<1907::AID-CNCR2820340609>3.0.CO
[8]  
2-4
[9]  
Banerjee NS, 2004, MOL CANCER THER, V3, P437
[10]   Combined transcriptional and transductional targeting improves the specificity and efficacy of adenoviral gene delivery to ovarian carcinoma [J].
Barker, SD ;
Dmitriev, IP ;
Nettelbeck, DM ;
Liu, B ;
Rivera, AA ;
Alvarez, RD ;
Curiel, DT ;
Hemminki, A .
GENE THERAPY, 2003, 10 (14) :1198-1204