Initiation of DNA synthesis in Ehrlich ascites tumor cells in their plateau phase of growth.
Burns Er
Abstract
Burns Er
Abstract
The E2 hypotetraploid Ehrlich ascites tumor reached its peak size at 1 × 109 cells on the 14th day after i.p. inoculation of 0.30 × 106 cells. During this period the % nonviable Ehrlich ascites tumor cells did not change. Autoradiographic studies during the first 14 days of Ehrlich ascites tumor growth demonstrated no decrease in the % tumor cells incorporating tritiated uridine, proline, phenylalanine, or leucine. The % Ehrlich ascites tumor cells in DNA synthesis (thymidine-3H incorporation), however, decreased with increasing tumor age. Aspiration of most of the tumorous ascitic fluid from a 14-day-old Ehrlich ascites tumor host resulted in recurrent growth of the remaining Ehrlich ascites tumor. Recurrent growth of the Ehrlich ascites tumor was characterized by a significant increase in the thymidine index (% Ehrlich ascites tumor cells incorporating thymdine-3H in 20 min). The peak thymidine index of recurrent growth, 51.8%, occurred between the 14th and 24th (19th) hr after aspiration of most of the 14-day-old tumorous ascitic fluid. During recurrent growth of the Ehrlich ascites tumor a lag period of at least 4 hr occurred between the time of ascites removal and the increase in the thymidine index. Thymidine index determinations made after transplantation of saline-washed 14-day-old Ehrlich ascites tumor cells to new hosts also demonstrated ( a ) a 4 hr lag period before the thymidine index began to increase and ( b ) a peak thymidine index, 56.1%, 19 hr after inoculation. The data are discussed in relation to the events in the cell cycle.
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The E2 hypotetraploid Ehrlich ascites tumor reached its peak size at 1 × 109 cells on the 14th day after i.p. inoculation of 0.30 × 106 cells. During this period the % nonviable Ehrlich ascites tumor cells did not change. Autoradiographic studies during the first 14 days of Ehrlich ascites tumor growth demonstrated no decrease in the % tumor cells incorporating tritiated uridine, proline, phenylalanine, or leucine. The % Ehrlich ascites tumor cells in DNA synthesis (thymidine-3H incorporation), however, decreased with increasing tumor age. Aspiration of most of the tumorous ascitic fluid from a 14-day-old Ehrlich ascites tumor host resulted in recurrent growth of the remaining Ehrlich ascites tumor. Recurrent growth of the Ehrlich ascites tumor was characterized by a significant increase in the thymidine index (% Ehrlich ascites tumor cells incorporating thymdine-3H in 20 min). The peak thymidine index of recurrent growth, 51.8%, occurred between the 14th and 24th (19th) hr after aspiration of most of the 14-day-old tumorous ascitic fluid. During recurrent growth of the Ehrlich ascites tumor a lag period of at least 4 hr occurred between the time of ascites removal and the increase in the thymidine index. Thymidine index determinations made after transplantation of saline-washed 14-day-old Ehrlich ascites tumor cells to new hosts also demonstrated ( a ) a 4 hr lag period before the thymidine index began to increase and ( b ) a peak thymidine index, 56.1%, 19 hr after inoculation. The data are discussed in relation to the events in the cell cycle.
Key concepts: Thymidine, Ascites, Ehrlich ascites, DNA synthesis, Neoplasm, Biology, Mitotic index, Tumor cells