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Monaldi Archives Of Chest Disease • April 1998<br />

The biological activities of simian virus 40<br />

large-T antigen and its possible oncogenic effects in humans<br />

Author information<br />

Matker CM1, Rizzo P, Pass HI, Di Resta I,<br />

Powers A, Mutti L, Kast WM, Carbone M.<br />

Cardinal Bernardin Cancer Center<br />

Loyola University of Chicago<br />

Maywood, IL 60153, USA<br />

Abstract<br />

Simian virus 40 (SV40) is an oncogenic virus which induces tumors in hamsters and transforms<br />

human cells in tissue culture. Between 1955 and 1963, polio vaccines and adenovaccines<br />

were contaminated with SV40; therefore, millions of people were exposed to this<br />

oncogenic virus. The SV40 proteins responsible for in vivo oncogenesis and in vitro cell<br />

transformation are encoded by the early region of the virus. These proteins are called T<br />

(tumor) antigens (Tags), because animals with tumors induced by SV40 have antibodies<br />

against these viral proteins. Recently, we and other research laboratories have found SV40<br />

in specific types of human tumors: mesothelioma, ependymoma and choroid plexus tumors,<br />

osteosarcoma and sarcoma. The same tumor types will develop in hamsters which have been<br />

injected systemically with SV40. SV40 causes cell transformation in tissue culture and tumors<br />

in animals, because SV40 Tag binds and inactivates the cellular tumor suppressor gene<br />

products, Rb and p53. We found that SV40 Tag binds p53 and Rb in human mesotheliomas,<br />

possibly contributing to the malignant phenotype.<br />

“Between 1955 and 1963,<br />

polio vaccines and adenovaccines<br />

were contaminated with SV40; therefore,<br />

millions of people were exposed<br />

to this oncogenic virus.”<br />

http://www.ncbi.nlm.nih.gov/pubmed/9689808

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