Effect of chemically modified polyamine analogues on biosynthesis of polyamines and putrescine in cell-free system of rat hepatoma

Nine novel chemically modified polyamine analogues were synthesized as potential antitumor agents and evaluated for their capacity to inhibit biosynthesis of polyamines in cell-free system of rat hepatoma G-27. All analogues (numbers I-IX) were used in a final concentration of 10 -4 M. Compounds I-VI modified by adenosine demonstrated activation both ODC activity (except substance I) and polyamine synthesis. The degree of activation depended on the length and quantity of methylene groups in the structure of the analogues. Compound I inhibited ODC activity stronger than its known inhibitor DFMO. On the other hand, substances VII-IX modified by two uracils significantly reduced polyamine levels as well as inhibited the ODC activity more effectively than DFMO. These results indicate that in cell-free system of rat hepatoma G-27 new analogues I and VII-IX are capable of to some extent inhibiting biosynthesis of polyamines. These drugs might also be useful both as experimental approaches for investigation of pecularities of polyamine metabolism, and possible application of these substances as antineoplastic agents.

Авторы
Fedoronchuk T.V. 1 , Syatkin S.P. 1 , Lulle Zh.I. , Yanson Ya.Ya. , Lidak Yu.M. , Berezov T.T. 1
Редакторы
-
Издательство
-
Номер выпуска
9
Язык
Русский
Страницы
256-258
Статус
Опубликовано
Подразделение
-
DOI
-
Номер
-
Том
116
Год
1993
Организации
  • 1 Department of Biochemistry, Russian People's Friendship Univ., Moscow, Russian Federation
Ключевые слова
eflornithine; ornithine decarboxylase; polyamine derivative; putrescine; antineoplastic agent; polyamine; spermidine; spermine; animal cell; antineoplastic activity; article; drug activity; drug synthesis; enzyme activity; liver cell carcinoma; nonhuman; polyamine metabolism; rat; animal; biosynthesis; cell free system; comparative study; drug effect; liver tumor; male; metabolism; structure activity relation; Animal; Antineoplastic Agents; Biogenic Polyamines; Cell-Free System; Comparative Study; Eflornithine; English Abstract; Liver Neoplasms, Experimental; Male; Ornithine Decarboxylase; Polyamines; Putrescine; Rats; Spermidine; Spermine; Structure-Activity Relationship
Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/973/