Download Advances in Cancer Research, Vol. 49 by George Klein (ed.), Sidney Weinhouse (ed.) PDF

By George Klein (ed.), Sidney Weinhouse (ed.)

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Reo. Biophys. 8, 523-557. , Moscovici, M. , and Moscovici, C. (1985). Virology 144, 73-79. , and Shin, S. J. Cell Biol. 82, 1-8. , and Shin, S. (1981). In “The Immune System” (C. M. Steinberg and I. ), Vol. 2, pp. 417-424. Karger, Basel. , Smith, R. , and Weber, M. J. ]. Virot. 42,602611. , and Graf, T. (1984). Proc. Natl. Acad. Sci. 81, 7122-7126. , and Graf, T. (1986). Cell 45, 49-356. RETROVIRAL ONCOGENES AND MYOGENIC DIFFERENTIATION 27 Kingston, R. , Baldwin, A. , and Sharp, P. A. (1985). Cell 41, 3-5.

Nearly two score oncogenes have been identified, and the majority were garnered through the agency of retroviruses, which were first implicated in the formation of tumors at the turn of the century (Hunter, 1984; van Beveren and Verma, 1985). Peyton Rous used a similar procedure in 1911to isolate a different agent (now known as the Rous sarcoma virus) which produced sarcomas in chickens (Rous, 1911). Over the ensuing years filtrates from tumors of many different animal species were found to contain agents that could induce abnormal growths (Gross, 1951, 1953a,b, 1958; Friend, 1957).

1973). When the entire viral complex (FBJ-MLV and FBJ-MSV) was injected, parosteal tumors developed. In addition, when FBJ-MSV was combined with another helper virus, again parosteal tumors were produced. A titer of at least 1,000 focus-forming units (FFUs) is needed to reliably produce tumors. , 1973). It is generally assumed that a tumor which produces virus is not transplantable into an immunocompetent mouse because the viral antigens evoke a vigorous immune response and the tumor is destroyed.

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