Developing Oncolytic Viruses for the Treatment of Cervical Cancer

被引:8
作者
Kalafati, Eleni [1 ]
Drakopoulou, Ekati [1 ]
Anagnou, Nicholas P. [1 ]
Pappa, Kalliopi I. [1 ,2 ]
机构
[1] Acad Athens BRFAA, Biomed Res Fdn, Ctr Basic Res, Lab Cell & Gene Therapy, Athens 11527, Greece
[2] Univ Athens, Sch Med, Dept Obstet & Gynecol 1, Athens 11528, Greece
关键词
oncolytic viruses; cervical cancer; virotherapy; viral vectors; cancer immunotherapy; innate immunity; adaptive immunity; CONDITIONALLY-REPLICATIVE ADENOVIRUS; CELL CARCINOMA ANTIGEN-2; PHASE-I; MEASLES-VIRUS; GENE-THERAPY; TUMOR-CELLS; SYNERGISTIC COMBINATION; ANTITUMOR VACCINATION; VIRAL REPLICATION; SINDBIS-VIRUS;
D O I
10.3390/cells12141838
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cervical cancer represents one of the most important malignancies among women worldwide. Current therapeutic approaches for cervical cancer are reported not only to be inadequate for metastatic cervical cancer, but are also considered as cytotoxic for several patients leading to serious side effects, which can have negative implications on the quality of life of women. Therefore, there is an urgent need for the development of innovative and effective treatment options. Oncolytic viruses can eventually become effective biological agents, since they preferentially infect and kill cancer cells, while leaving the normal tissue unaffected. Moreover, they are also able to leverage the host immune system response to limit tumor growth. This review aims to systematically describe and discuss the different types of oncolytic viruses generated for targeting cervical cancer cells, as well as the outcome of the combination of virotherapy with conventional therapies. Although many preclinical studies have evaluated the therapeutic efficacy of oncolytic viruses in cervical cancer, the number of clinical trials so far is limited, while their oncolytic properties are currently being tested in clinical trials for the treatment of other malignancies.
引用
收藏
页数:20
相关论文
共 111 条
[1]  
Arvin A, 2007, HUMAN HERPESVIRUSES: BIOLOGY, THERAPY, AND IMMUNOPROPHYLAXIS, P700
[2]   Evaluation of a selectively oncolytic adenovirus for local and systemic treatment of cervical cancer [J].
Bauerschmitz, GJ ;
Kanerva, A ;
Wang, MH ;
Herrmann, I ;
Shaw, DR ;
Strong, TV ;
Desmond, R ;
Rein, DT ;
Dall, P ;
Curiel, DT ;
Hemminki, A .
INTERNATIONAL JOURNAL OF CANCER, 2004, 111 (02) :303-309
[3]  
Bauerschmitz GJ, 2002, INT J ONCOL, V21, P1161
[4]   Adenovirus E1B 55-Kilodalton Protein: Multiple Roles in Viral Infection and Cell Transformation [J].
Blackford, Andrew N. ;
Grand, Roger J. A. .
JOURNAL OF VIROLOGY, 2009, 83 (09) :4000-4012
[5]   Replication-selective herpes simplex virus type 1 mutant therapy of cervical cancer is enhanced by low-dose radiation [J].
Blank, SV ;
Rubin, SC ;
Coukos, G ;
Amin, KM ;
Albelda, SM ;
Molnar-Kimber, KL .
HUMAN GENE THERAPY, 2002, 13 (05) :627-639
[6]   Talimogene Laherparepvec (T-VEC) and Other Oncolytic Viruses for the Treatment of Melanoma [J].
Bommareddy, Praveen K. ;
Patel, Anand ;
Hossain, Saamia ;
Kaufman, Howard L. .
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2017, 18 (01) :1-15
[7]   Cathelicidin bovine myeloid antimicrobial peptide (BMAP) 28 is involved in the inflammatory response against alpha-herpesviruses in the bovine nervous system [J].
Burucua, M. M. ;
Perez, S. E. ;
Odeon, A. C. ;
Cobo, E. R. ;
Quintana, S. ;
Marin, M. S. .
MOLECULAR IMMUNOLOGY, 2020, 122 :148-155
[8]  
Callaway HM, 2019, J VIROL, V93, DOI [10.1128/jvi.01542-18, 10.1128/JVI.01542-18]
[9]   ONCOLYTIC HERPES SIMPLEX VIRUS 1 (HSV-1) VECTORS: INCREASING TREATMENT EFFICACY AND RANGE THROUGH STRATEGIC VIRUS DESIGN [J].
Carson, J. ;
Haddad, D. ;
Bressman, M. ;
Fong, Y. .
DRUGS OF THE FUTURE, 2010, 35 (03) :183-195
[10]   A Phase I study of KH901, a conditionally replicating granulocyte-macrophage colony-stimulating factor Armed oncolytic adenovirus for the treatment of head and neck cancers [J].
Chang, Jianhua ;
Zhao, Xiaoying ;
Wu, Xianghua ;
Guo, Ye ;
Guo, Haiyi ;
Cao, Junnin ;
Guo, Yong ;
Lou, Delun ;
Yu, Dechao ;
Li, Jin .
CANCER BIOLOGY & THERAPY, 2009, 8 (08) :676-682