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 <front>
  <journal-meta>
   <journal-id journal-id-type="publisher-id">Russian Journal of Biological Physics and Chemisrty</journal-id>
   <journal-title-group>
    <journal-title xml:lang="en">Russian Journal of Biological Physics and Chemisrty</journal-title>
    <trans-title-group xml:lang="ru">
     <trans-title>АКТУАЛЬНЫЕ ВОПРОСЫ БИОЛОГИЧЕСКОЙ ФИЗИКИ И ХИМИИ</trans-title>
    </trans-title-group>
   </journal-title-group>
   <issn publication-format="print">2499-9962</issn>
  </journal-meta>
  <article-meta>
   <article-id pub-id-type="publisher-id">54332</article-id>
   <article-categories>
    <subj-group subj-group-type="toc-heading" xml:lang="ru">
     <subject>МЕДИЦИНСКАЯ БИОФИЗИКА И БИОФИЗИЧЕСКАЯ ХИМИЯ</subject>
    </subj-group>
    <subj-group subj-group-type="toc-heading" xml:lang="en">
     <subject>MEDICAL BIOPHYSICS AND BIOPHYSICAL CHEMISTRY</subject>
    </subj-group>
    <subj-group>
     <subject>МЕДИЦИНСКАЯ БИОФИЗИКА И БИОФИЗИЧЕСКАЯ ХИМИЯ</subject>
    </subj-group>
   </article-categories>
   <title-group>
    <article-title xml:lang="en">THE FEATURES OF TUMORAL 2-DEOXY-D-RIBOSE-1-PHOSPHATE GENERATION, ASSOCIATION WITH PRODUCTION OF REACTIVE OXYGEN SPECIES</article-title>
    <trans-title-group xml:lang="ru">
     <trans-title>ОСОБЕННОСТИ ГЕНЕРАЦИИ 2-ДЕЗОКСИ-D-РИБОЗО-1-ФОСФАТА ОПУХОЛЬЮ, СВЯЗЬ С ПРОДУКЦИЕЙ АКТИВНЫХ ФОРМ КИСЛОРОДА</trans-title>
    </trans-title-group>
   </title-group>
   <contrib-group content-type="authors">
    <contrib contrib-type="author">
     <name-alternatives>
      <name xml:lang="ru">
       <surname>Бакурова</surname>
       <given-names>Е. М.</given-names>
      </name>
      <name xml:lang="en">
       <surname>Bakurova</surname>
       <given-names>E. M.</given-names>
      </name>
     </name-alternatives>
     <email>32023@mail.ru</email>
     <xref ref-type="aff" rid="aff-1"/>
    </contrib>
   </contrib-group>
   <aff-alternatives id="aff-1">
    <aff>
     <institution xml:lang="ru">Донецкий национальный медицинский университет им. М. Горького</institution>
     <city>Донецк</city>
     <country>Россия</country>
    </aff>
    <aff>
     <institution xml:lang="en">Maksim Gorky National Medical University</institution>
     <city>Donetsk</city>
     <country>Russian Federation</country>
    </aff>
   </aff-alternatives>
   <pub-date publication-format="print" date-type="pub" iso-8601-date="2018-09-25T20:22:29+03:00">
    <day>25</day>
    <month>09</month>
    <year>2018</year>
   </pub-date>
   <pub-date publication-format="electronic" date-type="pub" iso-8601-date="2018-09-25T20:22:29+03:00">
    <day>25</day>
    <month>09</month>
    <year>2018</year>
   </pub-date>
   <volume>3</volume>
   <issue>3</issue>
   <fpage>584</fpage>
   <lpage>587</lpage>
   <history>
    <date date-type="received" iso-8601-date="2018-09-20T20:22:29+03:00">
     <day>20</day>
     <month>09</month>
     <year>2018</year>
    </date>
    <date date-type="accepted" iso-8601-date="2018-09-20T20:22:29+03:00">
     <day>20</day>
     <month>09</month>
     <year>2018</year>
    </date>
   </history>
   <self-uri xlink:href="https://rusjbpc.ru/en/nauka/article/54332/view">https://rusjbpc.ru/en/nauka/article/54332/view</self-uri>
   <abstract xml:lang="ru">
    <p>Выполнено сравнительное исследование активности ферментов обмена тимидина, аденозина и антиоксидантной системы в 44 образцах тканей эпителиальных опухолей распространенного рака желудка и кишечника (ЖКТ), немелкоклеточного рака легких (НМКРЛ). В качестве индивидуального контроля использовали нетрансформированные ткани края резекции. Выявлено повышение опухолевой активности тимидинфосфорилазы (ТФ) в 1,8 раза (p = 0,002) и аденозиндезаминазы (АДА) в 1,7 - 1,9 раз (p = 0,001); установлена корреляция трансферазной активности ТФ и АДА (ρ = 0,704; р &lt; 0,001). Это обеспечивает как продукцию 2-дезокси-D-рибозо-1-фосфата (2-д-D-Риб-1-Ф), так и ресинтез дезокситимидина, необходимого для синтеза дезокситимидилата по «запасному пути». При этом снижение активности глутатионпероксидазы способствует как усилению процессов гликирования в опухолях избыточной 2-д-D-Риб, так и повышению уровней Н2О2. Сделан вывод, что данные особенности обмена способствуют резонированию эффектов гликативного и оксидативного стрессов, сопровождающих опухолевую прогрессию.</p>
   </abstract>
   <trans-abstract xml:lang="en">
    <p>A comparative study of the enzymes activity of thymidine, adenosine metabolism and the activity of antioxidant defense enzymes in tumors of different localizations was carried out. Aim: to evaluate the relevance of thymidine phosphorylase (TP), adenosine deaminase (ADA) in 2-deoxy-D-ribose (2-d-D-R-1-P) formation and their association with superoxide dismutase, glutathione peroxidase activity in tumors. We demonstrated that tumor TP activity is higher by 1,8 times (p = 0,002), ADA activity is higher by 1,7-1,9 times (p = 0,001) as compared to non-neoplastic tissues of resection margin. The positive correlation between the intensity of TP and ADA activity was shown (the index of Spearman’s rank correlation, i.e. ρ = 0,704; р &lt; 0,001). So, tumors can increase the levels of 2-deoxy-D-ribose (2-d-D-R) and can stimulate of deoxythymidilate synthesis by the «salvage pathway» in one time. The nucleoside enzymes activity changes being accompanied by decrease of glutathione peroxidase activity in the tumors. Conclusion: It could be suggested that in cancers of different localizations the glycation by 2-d-D-R being associated with hydrogen peroxide formation. Here, we provide evidence on the impact and cooperation of glycative stress and oxidative stress in promoting human cancer progression.</p>
   </trans-abstract>
   <kwd-group xml:lang="ru">
    <kwd>ферменты</kwd>
    <kwd>2-дезокси-D-рибоза</kwd>
    <kwd>перекись водорода</kwd>
    <kwd>опухоль</kwd>
   </kwd-group>
   <kwd-group xml:lang="en">
    <kwd>enzymes</kwd>
    <kwd>2-deoxy-D-ribose</kwd>
    <kwd>hydrogen peroxide</kwd>
    <kwd>cancer</kwd>
   </kwd-group>
  </article-meta>
 </front>
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