Brain tumors and polyomaviruses

S Croul, J Otte, K Khalili - Journal of neurovirology, 2003 - Taylor & Francis
S Croul, J Otte, K Khalili
Journal of neurovirology, 2003Taylor & Francis
Polyomaviruses, including JC virus (JCV), BK virus (BKV), and simian virus 40 (SV40) have
attracted much attention in the past decade due to their repeated isolation from various
human tumors, including those originating from the central nervous system (CNS). JCV and
BKV are considered to be ubiquitous human pathogens that become reactivated under
impaired physiological conditions such as immunosuppression. Productive replication of
JCV and BKV induces diseases such as progressive multifocal leukoencephalopathy in the …
Polyomaviruses, including JC virus (JCV), BK virus (BKV), and simian virus 40 (SV40) have attracted much attention in the past decade due to their repeated isolation from various human tumors, including those originating from the central nervous system (CNS). JCV and BKV are considered to be ubiquitous human pathogens that become reactivated under impaired physiological conditions such as immunosuppression. Productive replication of JCV and BKV induces diseases such as progressive multifocal leukoencephalopathy in the brain and hemorrhagic or nonhemorrhagic cystitis and nephritis in the kidney. JCV DNA sequences have been isolated from a number of human CNS tumors, including medulloblastoma, ependymoma, and a broad range of glial-origin neoplasms. SV40, once believed to be a monkey virus, has now been isolated from a variety of human cancer cells, including mesothelioma, ependymoma, and non-Hodgkin's lymphoma. In this mini-review, the authors focused their attention on the possible involvement of polyomaviruses, such as JCV, BKV, and SV40, with human brain tumors.
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