Antitumor Agents LIV: The Effects of Daphnoretin on In Vitro Protein Synthesis of Ehrlich Ascites Carcinoma Cells and Other Tissues

1982 ◽  
Vol 71 (7) ◽  
pp. 745-749 ◽  
Author(s):  
Y.F. Liou ◽  
I.H. Hall ◽  
K.H. Lee
1965 ◽  
Vol 43 (7) ◽  
pp. 859-864 ◽  
Author(s):  
Shan-Ching Sung

The rate of DNA synthesis in Ehrlich ascites cells measured immediately after X-irradiation of 500 r for 6 minutes in vitro showed about 15% reduction. However, if X-irradiation was followed by preincubation of the cells, the subsequent synthesis of DNA in the X-irradiated cells was markedly inhibited. Under the same condition, the uptake of thymidine-2-C14, uridine-2-C14, adenine-8-C14, and glycine-1-C14, and protein synthesis in the X-irradiated cells were found to be almost the same as those in the non-irradiated control. RNA synthesis measured as total RNA was only slightly inhibited.


1995 ◽  
Vol 15 (3) ◽  
pp. 429-437 ◽  
Author(s):  
Y.M. Kwon ◽  
K.N. Heo ◽  
Y.J. Choi ◽  
I.K. Han ◽  
J.H. Woo

1965 ◽  
Vol 43 (2) ◽  
pp. 209-224 ◽  
Author(s):  
B. I. Uppin ◽  
P. G. Scholefield

Studies have been made of the effects of metabolic inhibitors on the oxidation and incorporation of radioactivity into nucleotides of glucose labelled in the 1, 2, and 6 positions. The results indicate that in Ehrlich ascites carcinoma cells the predominant oxidative pathway is the hexosemonophosphate shunt. Investigation of the time courses of oxidation of the labelled glucose molecules confirms this conclusion. The pattern of incorporation of radioactivity initially suggests that nucleotide ribose is not formed via this pathway. However, it is shown that the coupling of an active transketolase system with the other enzymes of the hexosemonophosphate shunt provides a sufficient explanation of all the experimental observations. The conclusion is reached that pentose is formed by oxidation of glucose through the shunt but that the labelling pattern is largely established as the result of the exchange reaction catalyzed by transketolase.


Author(s):  
Michael J. Leibowitz ◽  
Francis P. Barbone ◽  
Denise E. Georgopoulos

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