Use of an oncolytic vaccinia virus for the treatment of canine breast cancer in nude mice: preclinical development of a therapeutic agent

被引:40
作者
Gentschev, I. [1 ,2 ]
Stritzker, J. [1 ,2 ]
Hofmann, E. [2 ]
Weibel, S. [2 ]
Yu, Y. A. [1 ]
Chen, N. [1 ]
Zhang, Q. [1 ]
Bullerdiek, J. [3 ,4 ]
Nolte, I. [4 ]
Szalay, A. A. [1 ,2 ,5 ,6 ]
机构
[1] Genelux Corp, San Diego Sci Ctr, San Diego, CA 92109 USA
[2] Univ Wurzburg, Dept Biochem, Wurzburg, Germany
[3] Univ Bremen, Ctr Human Genet, Bremen, Germany
[4] Univ Vet Med, Small Anim Clin, Hannover, Germany
[5] Univ Wurzburg, Virchow Ctr Expt Biomed, Wurzburg, Germany
[6] Univ Wurzburg, Inst Mol Infect Biol, Wurzburg, Germany
关键词
oncolytic virotherapy; vaccinia virus; canine cancer therapy; MAMMARY-GLAND TUMORS; HERPES-SIMPLEX-VIRUS; ANTITUMOR-ACTIVITY; SYSTEMIC DELIVERY; DOGS; MICROENVIRONMENT; XENOGRAFTS; IMMUNITY; VECTORS; CELLS;
D O I
10.1038/cgt.2008.87
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
Mammary cancers together with cancers of the skin account for about 60% of the total cancers occurring in dogs. The veterinary options for therapeutic management of canine mammary cancer are limited and prognosis for such patients is poor. In this study, we analyzed the functionality of the oncolytic vaccinia virus strain GLV-1h68 as a possible therapeutic agent for canine mammary cancer. Cell culture data demonstrated that GLV-1h68 efficiently infected and destroyed cells of the canine mammary adenoma cell line ZMTH3. Furthermore, after systemic administration this attenuated vaccinia virus strain primarily replicated in canine tumor xenografts in nude mice. The efficient tumor colonization process resulted in inhibition of tumor growth and drastic reduction of tumor size. This is the first report demonstrating that vaccinia virus is an effective tool for the therapy of canine mammary cancers, which might next be applied to dogs with breast tumors.
引用
收藏
页码:320 / 328
页数:9
相关论文
共 37 条
[31]   Enhanced treatment of breast cancer brain metastases with oncolytic virus expressing anti-CD47 antibody and temozolomide [J].
Wang, Jing ;
Tian, Lei ;
Barr, Tasha ;
Jin, Lewei ;
Chen, Yuqing ;
Li, Zhiyao ;
Wang, Ge ;
Liu, Jian-Chang ;
Wang, Li-Shu ;
Zhang, Jianying ;
Hsu, David ;
Feng, Mingye ;
Caligiuri, Michael A. ;
Yu, Jianhua .
MOLECULAR THERAPY ONCOLOGY, 2024, 32 (03)
[32]   New Therapeutic Possibilities of Combined Treatment of Radiotherapy with Oxaliplatin and its Liposomal Formulation, Lipoxal™, in Rectal Cancer Using Xenograft in Nude Mice [J].
Tippayamontri, Thititip ;
Kotb, Rami ;
Sanche, Leon ;
Paquette, Benoit .
ANTICANCER RESEARCH, 2014, 34 (10) :5303-5312
[33]   Development of the oncolytic virus, CF33, and its derivatives for peritoneal-directed treatment of gastric cancer peritoneal metastases [J].
Yang, Annie ;
Zhang, Zhifang ;
Chaurasiya, Shyambabu ;
Park, Anthony K. ;
Jung, Audrey ;
Lu, Jianming ;
Kim, Sang-In ;
Priceman, Saul ;
Fong, Yuman ;
Woo, Yanghee .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2023, 11 (04)
[34]   A new therapeutic strategy for luminal A-breast cancer treatment: vulpinic acid as an anti-neoplastic agent induces ferroptosis and apoptosis mechanisms [J].
Alkan, Ayse Hale ;
Ensoy, Mine ;
Cansaran-Duman, Demet .
MEDICAL ONCOLOGY, 2024, 41 (09)
[35]   Therapeutic Potential of the Natural Compound S-Adenosylmethionine as a Chemoprotective Synergistic Agent in Breast, and Head and Neck Cancer Treatment: Current Status of Research [J].
Mosca, Laura ;
Vitiello, Francesca ;
Coppola, Alessandra ;
Borzacchiello, Luigi ;
Ilisso, Concetta Paola ;
Pagano, Martina ;
Caraglia, Michele ;
Cacciapuoti, Giovanna ;
Porcelli, Marina .
INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2020, 21 (22) :1-15
[36]   Preclinical rationale for combined use of endocrine therapy and 5-fluorouracil but neither doxorubicin nor paclitaxel in the treatment of endocrine-responsive breast cancer [J].
Kurebayashi, Junichi ;
Nukatsuka, Mamoru ;
Sonoo, Hiroshi ;
Uchida, Junji ;
Kiniwa, Mamoru .
CANCER CHEMOTHERAPY AND PHARMACOLOGY, 2010, 65 (02) :219-225
[37]   Mutant p53 as a therapeutic target for the treatment of triple-negative breast cancer: Preclinical investigation with the anti-p53 drug, PK11007 [J].
Synnott, Naoise C. ;
Bauer, Matthias R. ;
Madden, Stephen ;
Murray, Alyson ;
Klinger, Rut ;
O'Donovan, Norma ;
O'Connor, Darran ;
Gallagher, William M. ;
Crown, John ;
Fersht, Alan R. ;
Duffy, Michael J. .
CANCER LETTERS, 2018, 414 :99-106