DNA polymerase activities in fractionated walker-256 tumor cell nuclei

1970 ◽  
Vol 40 (5) ◽  
pp. 1201-1208 ◽  
Author(s):  
N. Raghuveer Ballal ◽  
Michael S. Collins ◽  
Richard M. Halpern ◽  
Roberts A. Smith
2004 ◽  
Vol 68 (11) ◽  
pp. 2197-2206 ◽  
Author(s):  
Claudia B.L. Campos ◽  
Giovanna R. Degasperi ◽  
Denise S. Pacífico ◽  
Luciane C. Alberici ◽  
Raquel S. Carreira ◽  
...  

2011 ◽  
Vol 36 (4) ◽  
pp. 533-538 ◽  
Author(s):  
Carina de Lima ◽  
Luciana Alves ◽  
Fabíola Iagher ◽  
Andressa Franzoi Machado ◽  
Marcelo Kryczyk ◽  
...  

Physical activity has been used in cancer prevention and treatment. In this study, we investigated some of the mechanisms by which anaerobic exercise reduces tumor growth. To do so, rats were trained for 8 weeks. Training consisted of jumping in a swimming pool for ten 30-s sets, with a load that was 50% of body weight attached to the back, 4 times per week. At the sixth week, anaerobic exercise trained rats (EX group) were inoculated with a suspension of Walker 256 tumor cells. Tumor weight, apoptotic tumor cells, tumor Bax and Bcl-2 protein expression, tumor lipid peroxidation, and tumor cell proliferation ex vivo were evaluated. Tumor weight was significantly lower in the EX group (∼30%) than in rats that did not undergo training (sedentary group) (p < 0.05). Apoptosis in the tumor cells of EX rats was 2-fold higher than in the tumor cells of sedentary rats; in addition, Bax expression increased by 10% and Bcl-2 decreased by 13% in EX rats. Lipid peroxidation was 4-fold higher in the tumor cells of EX rats than in those of sedentary rats (p < 0.05). Tumor cell proliferation ex vivo was 29% lower in the EX group than in the sedentary group (p < 0.05). In conclusion, Walker 256 tumor-bearing exercised rats presented more tumor cell apoptosis, a higher tumor content of lipid peroxides, pro-apoptotic protein expression balance, and reduced tumor weight and cell proliferation ex vivo, compared with sedentary rats. These events, together, account for the lower tumor growth we observed in the EX rats.


2019 ◽  
Vol 71 (1) ◽  
pp. 111-117 ◽  
Author(s):  
Sérgio Ricardo de Brito Bello ◽  
Katya Naliwaiko ◽  
Mariana Scudeller Vicentini ◽  
Francini Xavier Rossetti ◽  
Luiz Claudio Fernandes ◽  
...  

1978 ◽  
Vol 173 (1) ◽  
pp. 309-314 ◽  
Author(s):  
T R Butt ◽  
W M Wood ◽  
E L McKay ◽  
R L P Adams

The effects on DNA synthesis in vitro in mouse L929-cell nuclei of differential extraction of DNA polymerases alpha and beta were studied. Removal of all measurable DNA polymerase alpha and 20% of DNA polymerase beta leads to a 40% fall in the replicative DNA synthesis. Removal of 70% of DNA polymerase beta inhibits replicative synthesis by 80%. In all cases the nuclear DNA synthesis is sensitive to N-ethylmaleimide and aCTP (arabinosylcytosine triphosphate), though less so than DNA polymerase alpha. Addition of deoxyribonuclease I to the nuclear incubation leads to synthesis of high-molecular-weight DNA in a repair reaction. This occurs equally in nuclei from non-growing or S-phase cells. The former nuclei lack DNA polymerase alpha and the reaction reflects the sensitivity of DNA polymerase beta to inhibiton by N-ethylmaleimide and aCTP.


1990 ◽  
Vol 258 (6) ◽  
pp. E1033-E1036 ◽  
Author(s):  
L. C. Fernandes ◽  
U. F. Machado ◽  
C. R. Nogueira ◽  
A. R. Carpinelli ◽  
R. Curi

The effect of cachexia on insulin secretion was examined in adult male rats. Isolated islets of Langerhans from Walker 256 tumor-bearing rats secreted less insulin by glucose stimuli as compared with the control group; this was accompanied by significant change in 45Ca2+ outflow rate. Reduced insulin secretion to glucose stimuli in tumor-bearing rats probably led to low insulinemia (one-third). These findings indicate that reduced insulin secretion is probably an important factor for the development of cachexia in Walker 256 tumor-bearing rats.


Life Sciences ◽  
2007 ◽  
Vol 80 (10) ◽  
pp. 950-958 ◽  
Author(s):  
Andréia Buffon ◽  
Vanessa B. Ribeiro ◽  
Márcia R. Wink ◽  
Emerson A. Casali ◽  
João J.F. Sarkis

Sign in / Sign up

Export Citation Format

Share Document