Cell cultures of Syrian hamster -embryo were treated for 7 days with selected chemicals. Certain cultures were morphologically transformed by three different chemical preparations and yielded cell lines that subsequently produced malignant tumors in hamsters.Although the cell lines were negative for infectious virus before inoculation into animals, hamster-specific C-type RNA virus was isolated from tumors or from cell lines derived from the tumors. Since infectious C-type viruses are usually not demonstrable in hamster tissues of normal or tumor origin, we conclude that the chemical treatment and activation of the viruses are related events.Infectious leukemia viruses (C-type, RNA) have been isolated many times from different strains of chickens, mice, and cats (1). In contrast, infectious viruses capable of serial propagation have been isolated from hamsters only on rare occasions, mainly from tumors induced by murine sarcoma viruses (2-5). These viruses, termed "hamster specific", have an altered host range and do not share envelope or groupspecific (gs) antigens with the murine C-type viruses (6, 7). Nonsarcomagenic C-type viruses, isolated from stocks of the hamster sarcoma virus by endpoint dilution (5) or cloning techniques (8), share a gs antigen (7) with a noninfectious hamster C-type virus that was detected in a spontaneous lymphoma (9). The above data were interpreted as indicating in vivo rescue of the murine sarcoma virus genome by a hamster-specific leukemia virus (HaLV). Leukemia or integrated state in hamsters, and if so, how prevalent is the viral genome? In this paper we present evidence that the latent or repressed HaLV genome may be widely disseminated in hamster colonies, but can be activated and isolated only under certain conditions.
PROCEDURES AND RESULTS Cell transformation and tumor inductionCell cultures prepared from an early passage of hamster (LSH and NIH strains)-embryo cells were treated for 7 days with 0.1 ug/ml of the chemical carcinogen 3-methylcholanthrene, or with 0.1 or 1.0 yg/ml of certain fractions of cigarette-smoke condensate (12) dissolved in acetone and diluted in Eagle's Minimal Essential Medium with 10% fetalcalf serum. After the initial 7-day treatment, the chemicals were removed permanently and the cultures were subdivided as needed. Complete details of culture derivation and chemical treatment have been published (13). As summarized in Table 1, six of the chemically treated cell lines became transformed, based on changes in growth rates and morphological alterations after 5-10 subcultures (Figs. 1 and 2). The control cell lines remained normal; however, there was a marked variation in the growth characteristics of the cell pools used, with the F695 control culture becoming terminal after a few passages, and the F559 and F839 control cultures continuing to grow for at least 30 passages. Due to their lack of growth in culture, large numbers of F695 control cells were not available for inoculation into newborn hamsters. On the other hand, F839 and F559 con...