Advances in Cancer Research, Vol. 15 - download pdf or read online

By George Klein, Sidney Weinhouse, Alexander Haddow (Eds.)

ISBN-10: 0120066157

ISBN-13: 9780120066155

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Jensen and Defendi (1968) used the same technique to demonstrate the absence of SV40 TSTA in simian cells transformed by ultraviolet light-irradiated defective SV40 (PARA), However, it should be pointed out that these latter cells were not tested for their ability to immunize hamsters against challenge with an immunosensitive SV40 tumor cell line. This is an important point, since Lausch et al. (1968) showed that hamster cells transformed by defective SV40 (PARA) were not effective at preventing SV40 tumorigenesis, yet were rejected by SV40-immunized hamsters.

Extrachromosomal copies of the virus may exist, and these may be detected in the virus recovery attempts. Rescue experiments to date have not succeeded in eliciting infectious virus from more than a minor proportion of a transformed cell population. One type of PAPOVAVIRUS SV40 35 evidence which would be supportive would be the isolation of specialized transducing particles containing a portion of the viral genome linked to a region of the host cell DNA. Such particles would be analogous to Xdg (Campbell, 1957) and would arise as a result of excision a t the LLwrong’’ sites on the chromosome.

The biological function of T-antigen remains obscure. , 1969). This antigen has been localized in the perinuclear region of cells infected with a strain of adenovirus type 2 carrying a defective SV40 genome (AdB'ND,). Sera from monkeys immunized with cells infected with Ad2+ND, react with an intranuclear antigen present in both SV40-transformed and SV40infected cells (Lewis and Rowe, 1971). Antibody to U-antigen is also detected in sera from SV40 tumor-bearing hamsters. I n contrast to Tantigen, U-antigen is heat-stable.

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Advances in Cancer Research, Vol. 15 by George Klein, Sidney Weinhouse, Alexander Haddow (Eds.)

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