The RVP3 cell line established from an in vivo passaged RVP3 tumour, which originally arose in RSV-injected mice, was analyzed at different passage levels and characterized virologically and cytogenetically. The RVP3 cell line is characterized by the presence of 2 to 5 medium-sized to large metacentric chromosomes, the majority of the mitoses contain about 1 subtelocentric chromosome, and in addition, every mitosis contains several chromosomal structures corresponding to the group called m-ms that comprises both minute chromatin bodies and microchromosomes. In three monocellular clones derived from the RVP3 cell line with a similar karyological picture it was established that the number of m-ms increased proportionally to the total number of chromosomes in individual metaphases. It was verified that: the RVP3 cell population does not contain any transmissible agent producing chromosomal changes in mouse cells; RVP3 cells are highly malignant; no RSV could be rescued from the clone tested. The significance of m-ms is discussed.

The full recovery of mice (Mus Musculus C57BL/6 strain) from virus-induced sarcoma after treatment with a complex of DDMC delivery system and sncRNAs