Please use this identifier to cite or link to this item: https://rep.polessu.by/handle/123456789/33380
Title: Комплексный характер влияния полициклических ароматических углеводородов на метаболические процессы как важный фактор, определяющий особенности их канцерогенной активации
Other Titles: Complex nature of the influence of polycyclic aromatic hydrocarbons on the metabolic processes as an important determinant of their carcinogenic activation
Authors: Сыса, А.Г.
Панибрат, О.В.
Бабенко, А.С.
Шабуня, П.С.
Фатыхова, С.А.
Киселев, П.А.
Sysa, A.G.
Panibrat, O.V.
Babenko, A.S.
Shabunya, P.S.
Fatykhova, S.A.
Kiselev, P.A.
Keywords: полициклические ароматические углеводороды
канцерогенные свойства
опухолевая клеточная линия А549
Issue Date: 2014
Citation: Комплексный характер влияния полициклических ароматических углеводородов на метаболические процессы как важный фактор, определяющий особенности их канцерогенной активации / А. Г. Сыса, О. В. Панибрат, А. С. Бабенко [и др.] // Доклады Национальной академии наук Беларуси. ‒ 2014. ‒ Т. 58, № 1. ‒ С. 53‒56.
Abstract: In the article, the contribution of the monooxygenase component to the carcinogenic activation of a key procarcinogenic derivative of benzo(a)pyrene – 7,8-benzo(a)pyrenediol in lung adenocarcinoma cell line A549 was evaluated. It is shown that the contribution of the monooxygenase process under the experimental conditions in A549 cells is only 13%, which corresponds to a relatively low level of the constitutive expression of CYP1A1 and CYP1B1. The situation changes significantly when cells are exposed to 20-methylcholanthrene. In this case, the monooxygenase component in the carcinogenic activation of 7,8-benzo(a)pyrenediol has reached 25%. Moreover, 90% is accounted for a “complete” carcinogen – diolepoxide-2. As 20-methylcholanthrene is a polycyclic aromatic compound and exists with a benzo(a)pyrene in the tobacco smoke, this suggests that the entry into the body a whole pool of polycyclic aromatic hydrocarbons may significantly affect not only the level but also the direction of the carcinogenic PAH activation of individual compounds.
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