Mounting a strategic offense: fighting tumor vasculature with oncolytic viruses

被引:33
作者
Angarita, Fernando A. [1 ,2 ]
Acuna, Sergio A. [1 ]
Ottolino-Perry, Kathryn [1 ,2 ]
Zerhouni, Siham [1 ,2 ,3 ]
McCart, J. Andrea [1 ,2 ,4 ,5 ]
机构
[1] Univ Hlth Network, Toronto Gen Res Inst, Div Expt Therapeut, Toronto, ON M5G 2M1, Canada
[2] Univ Toronto, Inst Med Sci, Toronto, ON M5S 1A8, Canada
[3] Univ British Columbia, Dept Surg, Vancouver, BC V5Z 4E3, Canada
[4] Mt Sinai Hosp, Dept Surg, Toronto, ON M5G 1X5, Canada
[5] Univ Toronto, Dept Surg, Toronto, ON M5G 1L5, Canada
基金
加拿大健康研究院;
关键词
oncolytic virotherapy; oncolytic virus; tumor vasculature; antivascular therapy; angiogenesis inhibitors; vascular disruption; HERPES-SIMPLEX-VIRUS; POTENT ANTITUMOR EFFICACY; VACCINIA VIRUS; PHASE-I; ANGIOGENESIS INHIBITION; THERAPEUTIC-EFFICACY; ENDOTHELIAL-CELLS; CANCER; ADENOVIRUS; GROWTH;
D O I
10.1016/j.molmed.2013.02.008
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
Blood supply within a tumor drives progression and ultimately allows for metastasis. Many anticancer therapies target tumor vasculature, but their individual effectiveness is limited because they induce indirect cell death. Agents that disrupt nascent and/or established tumor vasculature while simultaneously killing cancer cells would certainly have a greater impact. Oncolytic virotherapy utilizes attenuated viruses that replicate specifically within a tumor. They induce cytotoxicity through a combination of direct cell lysis, antitumor immune stimulation, and recently identified antitumor vascular effects. This review summarizes the novel preclinical and clinical evidence regarding the antitumor vascular effects of oncolytic viruses, which include infection and lysis of tumor endothelial cells, natural or genetically engineered antiangiogenic properties, and combination therapy with clinically approved antivascular agents.
引用
收藏
页码:378 / 392
页数:15
相关论文
共 108 条
[1]   Angiogenic response caused by oncolytic herpes simplex virus-induced reduced thrombospondin expression can be prevented by specific viral mutations or by administering a thrombospondin-derived peptide [J].
Aghi, Manish ;
Rabkin, Samuel D. ;
Martuza, Robert L. .
CANCER RESEARCH, 2007, 67 (02) :440-444
[2]   Hypoxia Enhances the Replication of Oncolytic Herpes Simplex Virus [J].
Aghi, Manish K. ;
Liu, Ta-Chiang ;
Rabkin, Samuel ;
Martuza, Robert L. .
MOLECULAR THERAPY, 2009, 17 (01) :51-56
[3]   Oncolytic HSV exerts direct antiangiogenic activity in ovarian carcinoma [J].
Benencia, F ;
Courreges, MC ;
Conejo-García, JR ;
Buckanovich, RJ ;
Zhang, L ;
Carroll, RH ;
Morgan, MA ;
Coukos, G .
HUMAN GENE THERAPY, 2005, 16 (06) :765-778
[4]   Tumorigenesis and the angiogenic switch [J].
Bergers, G ;
Benjamin, LE .
NATURE REVIEWS CANCER, 2003, 3 (06) :401-410
[5]   Modes of resistance to anti-angiogenic therapy [J].
Bergers, Gabriele ;
Hanahan, Douglas .
NATURE REVIEWS CANCER, 2008, 8 (08) :592-603
[6]   p53 inhibits hypoxia-inducible factor-stimulated transcription [J].
Blagosklonny, MV ;
An, WG ;
Romanova, LY ;
Trepel, J ;
Fojo, T ;
Neckers, L .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (20) :11995-11998
[7]   Targeted inflammation during oncolytic virus therapy severely compromises tumor blood flow [J].
Breitbach, Caroline J. ;
Paterson, Jennifer M. ;
Lemay, Chantal G. ;
Falls, Theresa J. ;
McGuire, Allison ;
Parato, Kelley A. ;
Stojdl, David F. ;
Daneshmand, Manijeh ;
Speth, Kelly ;
Kirn, David ;
McCart, J. Andrea ;
Atkins, Harold ;
Bell, John C. .
MOLECULAR THERAPY, 2007, 15 (09) :1686-1693
[8]   Oncolytic Vaccinia Virus Disrupts Tumor-Associated Vasculature in Humans [J].
Breitbach, Caroline J. ;
Arulanandam, Rozanne ;
De Silva, Naomi ;
Thorne, Steve H. ;
Patt, Richard ;
Daneshmand, Manijeh ;
Moon, Anne ;
Ilkow, Carolina ;
Burke, James ;
Hwang, Tae-Ho ;
Heo, Jeong ;
Cho, Mong ;
Chen, Hannah ;
Angarita, Fernando A. ;
Addison, Christina ;
McCart, J. Andrea ;
Bell, John C. ;
Kirn, David H. .
CANCER RESEARCH, 2013, 73 (04) :1265-1275
[9]   Targeting Tumor Vasculature With an Oncolytic Virus [J].
Breitbach, Caroline J. ;
De Silva, Naomi S. ;
Falls, Theresa J. ;
Aladl, Usaf ;
Evgin, Laura ;
Paterson, Jennifer ;
Sun, Yang Yang ;
Roy, Dominic G. ;
Rintoul, Julia L. ;
Daneshmand, Manijeh ;
Parato, Kelley ;
Stanford, Marianne M. ;
Lichty, Brian D. ;
Fenster, Aaron ;
Kirn, David ;
Atkins, Harold ;
Bell, John C. .
MOLECULAR THERAPY, 2011, 19 (05) :886-894
[10]  
Chaplin DJ, 1999, ANTICANCER RES, V19, P189