Selection of a highly invasive neuroblastoma cell population through long-term human cytomegalovirus infection

• Published in: Oncogenesis (New York, NY) Vol. 1; no. 4; p. e10
• Main Authors: Michaelis, M, Barth, S, Breitling, R, Bruch, J, Steinberger, D, Rothweiler, F, Hackmann, K, Schröck, E, Doerr, H W, Griffin, D K, Cinatl, J
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 01.04.2012; Nature Publishing Group
• Subjects: 692/699/67/1858; 692/699/67/1922; Apoptosis; Cell Biology; Human cytomegalovirus; Human Genetics; Internal Medicine; Medicine; Medicine & Public Health; Oncology; Original; original-article; neuroblastoma; cancer cell malignancy; oncomodulation; human cytomegalovirus; long-term infection
• ISSN: 2157-9024; 2157-9024
• DOI: 10.1038/oncsis.2012.10

The human cytomegalovirus (HCMV) is suspected to increase tumour malignancy by infection of cancer and/or stroma cells (oncomodulation). So far, oncomodulatory mechanisms have been attributed to the presence of HCMV and direct action of its gene products on cancer cells. Here, we investigated whether the prolonged presence of HCMV can result in the irreversible selection of a cancer cell population with increased malignancy. The neuroblastoma cell line UKF-NB-4 was long-term (200 passages) infected with the HCMV strain Hi91 (UKF-NB-4 Hi ) before virus eradication using ganciclovir (UKF-NB-4 HiGCV ). Global gene expression profiling of UKF-NB-4, UKF-NB-4 Hi and UKF-NB-4 HiGCV cells and subsequent bioinformatic signal transduction pathway analysis revealed clear differences between UKF-NB-4 and UKF-NB-4 Hi , as well as between UKF-NB-4 and UKF-NB-4 HiGCV cells, but only minor differences between UKF-NB-4 Hi and UKF-NB-4 HiGCV cells. Investigation of the expression of a subset of five genes in different chronically HCMV-infected cell lines before and after virus eradication suggested that long-term HCMV infection reproducibly causes specific changes. Array comparative genomic hybridisation showed virtually the same genomic differences for the comparisons UKF-NB-4 Hi /UKF-NB-4 and UKF-NB-4 HiGCV /UKF-NB-4. UKF-NB-4 Hi cells are characterised by an increased invasive potential compared with UKF-NB-4 cells. This phenotype was completely retained in UKF-NB-4 HiGCV cells. Moreover, there was a substantial overlap in the signal transduction pathways that differed significantly between UKF-NB-4 Hi /UKF-NB-4 HiGCV and UKF-NB-4 cells and those differentially regulated between tumour tissues from neuroblastoma patients with favourable or poor outcome. In conclusion, we present the first experimental evidence that long-term HCMV infection can result in the selection of tumour cell populations with enhanced malignancy.