Oncolytic virotherapy for urological cancers

被引:17
|
作者
Delwar, Zahid [1 ]
Zhang, Kaixin [2 ]
Rennie, Paul S. [3 ]
Jia, William [1 ]
机构
[1] Univ British Columbia, Dept Surg, 2211 Wesbrook Mall, Vancouver, BC V6T 2B5, Canada
[2] Univ British Columbia, Dept Urol, Level 6,2775 Laurel St, Vancouver, BC V5Z 1M9, Canada
[3] Vancouver Gen Hosp, Prostate Res Ctr, 2660 Oak St, Vancouver, BC V6H 3Z6, Canada
关键词
HERPES-SIMPLEX-VIRUS; VESICULAR STOMATITIS-VIRUS; PHASE-I TRIAL; NEWCASTLE-DISEASE VIRUS; STEM-CELL ANTIGEN; CONDITIONALLY REPLICATIVE ADENOVIRUS; SYNERGISTIC ANTITUMOR-ACTIVITY; DECAY-ACCELERATING FACTOR; BACILLUS-CALMETTE-GUERIN; SUICIDE GENE-THERAPY;
D O I
10.1038/nrurol.2016.84
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Oncolytic virotherapy is a cancer treatment in which replication-competent viruses are used that specifically infect, replicate in and lyse malignant tumour cells, while minimizing harm to normal cells. Anecdotal evidence of the effectiveness of this strategy has existed since the late nineteenth century, but advances and innovations in biotechnological methods in the 1980s and 1990s led to a renewed interest in this type of therapy. Multiple clinical trials investigating the use of agents constructed from a wide range of viruses have since been performed, and several of these enrolled patients with urological malignancies. Data from these clinical trials and from preclinical studies revealed a number of challenges to the effectiveness of oncolytic virotherapy that have prompted the development of further sophisticated strategies. Urological cancers have a range of distinctive features, such as specific genetic mutations and cell surface markers, which enable improving both effectiveness and safety of oncolytic virus treatments. The strategies employed in creating advanced oncolytic agents include alteration of the virus tropism, regulating transcription and translation of viral genes, combination with chemotherapy, radiotherapy or gene therapy, arming viruses with factors that stimulate the immune response against tumour cells and delivery technologies to ensure that the viral agent reaches its target tissue.
引用
收藏
页码:334 / 352
页数:19
相关论文
共 50 条
  • [21] Advances in oncolytic virotherapy
    Stephen J. Russell
    John C. Bell
    Christine E. Engeland
    Grant McFadden
    Communications Medicine, 2
  • [22] Personalizing oncolytic virotherapy?
    Kaur, Balveen
    Chiocca, E. Antonio
    MOLECULAR THERAPY, 2007, 15 (01) : 6 - 7
  • [23] Poxvirus oncolytic virotherapy
    Torres-Dominguez, Lino E.
    McFadden, Grant
    EXPERT OPINION ON BIOLOGICAL THERAPY, 2019, 19 (06) : 561 - 573
  • [24] Oncolytic virotherapy: the questions and the promise
    Aurelian, Laure
    ONCOLYTIC VIROTHERAPY, 2013, 2 : 19 - 29
  • [25] The combination therapy of oncolytic virotherapy
    Wang, Yue
    Zhu, Mengying
    Chi, Huanyu
    Liu, Yang
    Yu, Guilin
    FRONTIERS IN PHARMACOLOGY, 2024, 15
  • [26] Oncolytic Virotherapy and the Tumor Microenvironment
    Berkey, Sara E.
    Thorne, Steve H.
    Bartlett, David L.
    TUMOR IMMUNE MICROENVIRONMENT IN CANCER PROGRESSION AND CANCER THERAPY, 2017, 1036 : 157 - 172
  • [27] Oncolytic virotherapy for ovarian cancer
    Li, Shoudong
    Tong, Jessica
    Rahman, Masmudur M.
    Shepherd, Trevor G.
    McFadden, Grant
    ONCOLYTIC VIROTHERAPY, 2012, 1 : 1 - 21
  • [28] Cancer virotherapy with oncolytic adenoviruses
    Alemany, R.
    HUMAN GENE THERAPY, 2016, 27 (11) : A20 - A20
  • [29] Oncolytic Virotherapy for Hematological Malignancies
    Bais, Swarna
    Bartee, Eric
    Rahman, Masmudur M.
    McFadden, Grant
    Cogle, Christopher R.
    ADVANCES IN VIROLOGY, 2012, 2012
  • [30] Immunotherapeutic potential of oncolytic virotherapy
    Prestwich, Robin J.
    Harrington, Kevin J.
    Vile, Richard G.
    Melcher, Alan A.
    LANCET ONCOLOGY, 2008, 9 (07): : 610 - 612