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[Cancer Research 28, 1191-1196, June 1, 1968]
© 1968 American Association for Cancer Research

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Initiation of DNA Synthesis in Ehrlich Ascites Tumor Cells in Their Plateau Phase of Growth1

E. Robert Burns2,3

Department of Anatomy, Tulane University, New Orleans, Louisiana 70112

The E2 hypotetraploid Ehrlich ascites tumor reached its peak size at 1 x 109 cells on the 14th day after i.p. inoculation of 0.30 x 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.

1 Prepared in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Anatomy at Tulane University.

2 This work was done while the author was a Public Health Service Predoctoral Trainee. Part of this work was supported by National Science Foundation Grant G 23866 administered by Dr. S. Meryl Rose and a Greater New Orleans American Cancer Society Grant administered by Dr. Ralph N. Baillif.

3 Present address: Department of Anatomy, The University of Arkansas Medical Center, Little Rock, Arkansas 72201.

Received 7/21/67. Accepted 3/ 1/68.







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Copyright © 1968 by the American Association for Cancer Research.