Uncovering the Anticancer Potential of Murine Cytomegalovirus against Human Colon Cancer Cells

被引:3
|
作者
Massara, Layal [1 ,2 ]
Khairallah, Camille [1 ]
Yared, Nathalie [1 ]
Pitard, Vincent [1 ,2 ,3 ]
Rousseau, Benoit [4 ]
Izotte, Julien [4 ]
Giese, Alban [5 ]
Dubus, Pierre [5 ]
Gauthereau, Xavier [6 ]
Dechanet-Merville, Julie [1 ,2 ,3 ]
Capone, Myriam [1 ,2 ,6 ]
机构
[1] Univ Bordeaux, ImmunoConcEpT, CNRS, UMR 5164, F-33076 Bordeaux, France
[2] Equipe Labellisee Ligue Canc, Toulouse, France
[3] Univ Bordeaux, Plateforme Cytometrie, TBM Core, INSERM,CNRS,UMS 3427, F-33076 Bordeaux, France
[4] Univ Bordeaux, Serv Commun Animaleries, Animalerie A2, F-33076 Bordeaux, France
[5] Univ Bordeaux, Histol & Pathol Mol Tumeurs EA2406, F-33076 Bordeaux, France
[6] Univ Bordeaux, Plateforme PCR Quantitat, TBM Core, INSERM,CNRS,UMS 3427, F-33076 Bordeaux, France
来源
关键词
RELAPSE RISK EVIDENCE; EARLY GENE-EXPRESSION; DELTA-T-CELLS; COLORECTAL-CANCER; INTRATUMORAL INFECTION; CMV REACTIVATION; APOPTOSIS; TRANSPLANTATION; INTERFERON; GLIOBLASTOMA;
D O I
10.1016/j.omto.2020.01.007
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human cytomegalovirus (HCMV) components are often found in tumors, but the precise relationship between HCMV and cancer remains a matter of debate. Pro-tumor functions of HCMV were described in several studies, but an association between HCMV seropositivity and reduced cancer risk was also evidenced, presumably relying on recognition and killing of cancer cells by HCMV-induced lymphocytes. This study aimed at deciphering whether CMV influences cancer development in an immune-independent manner. Using immunodeficient mice, we showed that systemic infection with murine CMV (MCMV) inhibited the growth of murine carcinomas. Surprisingly, MCMV, but not HCMV, also reduced human colon carcinoma development in vivo. In vitro, both viruses infected human cancer cells. Expression of human interferon-beta (IFN-beta) and nuclear domain (ND10) were induced in MCMV-infected, but not in HCMV-infected human colon cancer cells. These results suggest a decreased capacity of MCMV to counteract intrinsic defenses in the human cellular host. Finally, immunodeficient mice receiving peri-tumoral MCMV therapy showed a reduction of human colon cancer cell growth, albeit no clinical sign of systemic virus dissemination was evidenced. Our study, which describes a selective advantage of MCMV over HCMV to control human colon cancer, could pave the way for the development of CMV-based therapies against cancer.
引用
收藏
页码:250 / 261
页数:12
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