Intensity of free-radical reactions in metastasizing cervical cancer.

2021 ◽  
Vol 39 (15_suppl) ◽  
pp. e17508-e17508
Author(s):  
Natalia V. Chernikova ◽  
Irina A. Goroshinskaya ◽  
Elena M. Frantsiyants ◽  
Ekaterina V. Verenikina ◽  
Yuriy A. Poryvaev ◽  
...  

e17508 Background: Cervical cancer (CC) is one of the main causes of death among patients with gynecological tumors. As a rule, patients die from relapses and metastases which rates reach 30-45%. According to research data, treatment of patients with distant metastases is ineffective, and half of them die within 9.7 months, while the average survival is 15.9±0.26 months. The development of many pathological processes is considered to be associated with an increase in free-radical reactions leading to oxidative damage to various biomolecules. The purpose of the study was to analyze some characteristics of the free-radical oxidation and antioxidant defence in metastasizing CC. Methods: The study included 56 patients aged 29-73 years with stage IIB-IV CC after antitumor treatment. The main group – 27 patients who developed metastases within 4 months to 8 years after the CC diagnosis; controls – 29 patients with non-metastatic CC; donors – 19 healthy women aged 27-61 years. The accumulation of carbonyl derivatives in blood plasma proteins was detected in the reaction with 2, 4-dinitrophenylhydrazine. The induced oxidative modification of proteins was stimulated with Fenton's reagent. Free-radical processes was evaluated by the intensity of peroxide-induced luminol-dependent plasma chemiluminescence and the content of nitric oxide metabolites; the intensity of lipid peroxidation - by the content of malondialdehyde (MDA); the activity of catalase and ceruloplasmin was also studied. Results: CC progression was accompanied by increasing lipid peroxidation and spontaneous oxidation of blood plasma proteins. MDA levels in patients with metastases increased by 57.8% compared to donors and by 34.3% compared to patients without metastases (p < 0.05). The concentration of 2, 4-dinitrophenylhydrozones increased on average by 4 times compared to donors and by almost 2 times compared to patients without metastases. Patients with metastasizing CC demonstrated elevated levels of products of the interaction of nitric oxide and its derivatives with proteins and peptides - 3-nitrotyrosine and nitrosoglutathione, compared to both donors (by 31.4% and 55.3%) and patients in remission (by 38.1% and 34.5%). Chemiluminescence activity increased by 54.5% compared to donors (p < 0.05) and by 93% (p < 0.01) compared to controls. Catalase activity in the blood plasma of patients with metastases increased by 54.1% compared to donors, but was lower than the values in the control group (by 22.1%). Ceruloplasmin activity was increased only in patients without metastases (by 33%). Conclusions: The process of CC metastasis is accompanied by a greater intensity of oxidative processes of both proteins and lipids, as well as depletion of the adaptive capabilities of the body's antioxidant system.

2007 ◽  
Vol 415 (1) ◽  
pp. 222-224 ◽  
Author(s):  
M. Ia. Akhalaia ◽  
A. A. Baizhumanov ◽  
N. A. Brazhe ◽  
O. G. Luneva ◽  
I. V. Mikhailov ◽  
...  

1982 ◽  
Vol 57 (2) ◽  
pp. 247-253 ◽  
Author(s):  
Edward D. Hall ◽  
J. Mark Braughler

✓ The present study was undertaken to examine the ability of a single large intravenous dose of methylprednisolone (15, 30, or 60 mg/kg) to attenuate lipid peroxidation and enhance (Na+ + K+)-ATPase activity during the 1st hour after a 400 gm-cm injury to the cat spinal cord. The contusion injury was associated with a rise in the concentration of fluorescent lipid peroxy products in the injured segment at 1 hour. In addition, the accumulation of cyclic guanosine 3″,5″-monophosphate (cyclic GMP), which was used as a new index of injury-induced free radical reactions, in the injured spinal segment was twice control levels. The injury-induced increase in fluorescence and cyclic GMP content in the contused spinal segment at 1 hour was completely prevented by the administration of 15 or 30 mg/kg of methylprednisolone at 30 minutes after injury. A 60-mg/kg dose, however, did not prevent the elevation in cyclic GMP. A concomitant examination of the acute effects of glucocorticoid administration on (Na+ + K+)-ATPase activity in the injured cord revealed a striking increase of enzyme activity after the 30-mg/kg dose, but a depression in activity with the 60-mg/kg dose. These results demonstrate that a single massive dose of methylprednisolone can beneficially reduce free-radical reactions and lipid peroxidation as well as enhance the activity of neuronal (Na+ + K+)-ATPase during the early phase after spinal cord contusion. The requirement for doses to be in the range of 15 to 30 mg/kg in order to produce these neurochemical changes is consistent with other studies that have demonstrated significantly greater recovery and tissue preservation in spinal cord-injured animals treated with comparable doses of methylprednisolone soon after injury. These findings suggest the need for a rigorous approach to glucocorticoid therapy in central nervous system trauma.


1998 ◽  
Vol 19 (4-5) ◽  
pp. 221-357 ◽  
Author(s):  
Jason P. Eiserich ◽  
Rakesh P. Patel ◽  
Valerie B. O’Donnell

1978 ◽  
Vol 56 (20) ◽  
pp. 2665-2672 ◽  
Author(s):  
L. Ross C. Barclay ◽  
Derek Leigh Carson ◽  
Jean A. Gray ◽  
Michael Grossman ◽  
Prabhaker G. Khazanie ◽  
...  

Ultraviolet irradiation of hydrocarbon solutions of 2,4,6-tri-tert-butylnitrosobenzene (1) formed [Formula: see text] The initial products were 2-methyl-1-nitroso-2-(3,5-di-tert-butyl)-phenylpropane (Ar—C(CH3)2CH2NO)2 (3) and a mixed dimer (4). Secondary and minor photoproducts isolated included 2-methyl-2-(3,5-di-tert-butyl)phenylpropanal oxime (5), 2-methyl-2-(3,5-di-tert-butyl)phenylpropanal (6) derived from 5, and 1,3,5-tri-tert-butylbenzene (7). The initial products are explained by formation of a tri-tert-butylphenyl radical (15), rearrangement of a hydrogen atom from an orthotert-butyl to the ring in 15, and rapid recombination of the neophyl radical with nitric oxide. Photolysis of 2,5-di-tert-butylnitrosobenzene (2) initially gave [Formula: see text] (10). Product analysis indicated a comparatively complex mixture including 1,4-di-tert-butylbenzene (11), 2,5-di-tert-butylphenol (12), and 2,5-di-tert-butylanilino-p-(2,5-di-tert-butyl)quinone (13). Evidence indicates that 12 and 13 form from free radical reactions involving 10 and the 2,5-di-tert-butylphenyl radical. The different photochemistry of 1 and 2 is discussed in terms of differential steric and conformational effects on the nitroso function which also is evident in their ultraviolet spectra.


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