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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Oncology</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Oncology</journal-title><trans-title-group xml:lang="ru"><trans-title>Российский онкологический журнал</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1028-9984</issn><issn publication-format="electronic">2412-9119</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">40408</article-id><article-id pub-id-type="doi">10.18821/1028-9984-2017-22-3-149-152</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">TISSUE GROWTH FACTORS OF VEGF FAMILY IN DYNAMICS OF THE DEVELOPMENT OF OVARIAN CANCER</article-title><trans-title-group xml:lang="ru"><trans-title>ТКАНЕВЫЕ ФАКТОРЫ РОСТА СЕМЕЙСТВА VEGF В ДИНАМИКЕ РАЗВИТИЯ РАКА ЯИЧНИКОВ</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kit</surname><given-names>O. I</given-names></name><name xml:lang="ru"><surname>Кит</surname><given-names>О. И</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Frantsiyants</surname><given-names>E. M</given-names></name><name xml:lang="ru"><surname>Франциянц</surname><given-names>Е. М</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Moiseenko</surname><given-names>T. I</given-names></name><name xml:lang="ru"><surname>Моисеенко</surname><given-names>Т. И</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Verenikina</surname><given-names>E. V</given-names></name><name xml:lang="ru"><surname>Вереникина</surname><given-names>Е. В</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Cheryarina</surname><given-names>N. D</given-names></name><name xml:lang="ru"><surname>Черярина</surname><given-names>Н. Д</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kozlova</surname><given-names>Larisa S.</given-names></name><name xml:lang="ru"><surname>Козлова</surname><given-names>Лариса Степановна</given-names></name></name-alternatives><bio xml:lang="en"><p>MD, PhD, Senior Researcher, Rostov-on-Don, 344037, Russian Federation.</p></bio><bio xml:lang="ru"><p>канд. биол. наук, доцент, старший научный сотрудник; 344037, г. Ростов-на-Дону, ул. 14-я линия, д. 63.</p></bio><email>super.gormon@ya.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Pogorelova</surname><given-names>Yu. A</given-names></name><name xml:lang="ru"><surname>Погорелова</surname><given-names>Ю. А</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Rosenko</surname><given-names>L. Ya</given-names></name><name xml:lang="ru"><surname>Розенко</surname><given-names>Л. Я</given-names></name></name-alternatives><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Rostov Research Institute of Oncology</institution></aff><aff><institution xml:lang="ru">ФГБУ «Ростовский научно-исследовательский онкологический институт» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2017-06-15" publication-format="electronic"><day>15</day><month>06</month><year>2017</year></pub-date><volume>22</volume><issue>3</issue><issue-title xml:lang="en">VOL 22, NO3 (2017)</issue-title><issue-title xml:lang="ru">ТОМ 22, №3 (2017)</issue-title><fpage>149</fpage><lpage>152</lpage><history><date date-type="received" iso-8601-date="2020-07-22"><day>22</day><month>07</month><year>2020</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2017, Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2017, ООО "Эко-Вектор"</copyright-statement><copyright-year>2017</copyright-year><copyright-holder xml:lang="en">Eco-Vector</copyright-holder><copyright-holder xml:lang="ru">ООО "Эко-Вектор"</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://rjonco.com/1028-9984/article/view/40408">https://rjonco.com/1028-9984/article/view/40408</self-uri><abstract xml:lang="en"><p>Ovarian carcinoma is the leading cause of death from gynecological cancer. Aim of the study is to reveal the role of VEGF-C comparing to VEGF-А in the progression of ovarian cancer. Material and methods. Tissue samples obtained from 76 patients with epithelial ovarian cancer (serous cystadenocarcinoma: T1N0M0; T2N0M0; T3NxM0; T4Nx-1M0) and 47 patients with cystadenoma were studied. Histological control was performed in all cases. Ovaries of 20 patients obtained during the surgery for uterine myoma were used as the intact tissue. All patients were 50.9 ± 2.9 years old. Levels of the growth factor as VEGF-A and its receptor VEGF-R1, as well VEGF-С and its receptor sVEGF-R3 - were measured by ELISA with the use of standard test systems. Results. VEGF-А levels in cystadenomas and intact tissue were similar, while in cystadenocarcinomas VEGF-А was significantly higher at all stages of the tumor development. sVEGF-R1 receptor in cystadenomas was lower in comparison with the intact tissue, in the contralateral ovary in T1N0M0 and in the tumorous ovary in T4Nx-1M0. VEGF-С level was higher significantly in all tumors, in cystadenocarcinomas it was higher if compared to cystadenomas. Its increase in the contralateral ovary in T1N0M0 differed from other tissue values being average. sVEGF-R3 receptor increased significantly at the later stages of ovarian cancer - T3NxM0 and T4Nx-1M0; its level was low only in the contralateral ovary in T1N0M0, and the values in other tissues were similar to the intact ones. Conclusion. The results show a high rate of lymphatic vessel formation in benign tumors at all stages of the development of the malignant tumor. The significant increase in VEGF-C level in the contralateral (non-tumorous) ovaries, compared to the intact tissue, allows considering VEGF-C, along with VEGF-А, as a pathogenetic factor of ovarian tumor development.</p></abstract><trans-abstract xml:lang="ru"><p>Карцинома яичника является ведущей причиной смерти от гинекологических опухолей. Цель исследования: выяснение роли VEGF-C в сравнительном аспекте с VEGF-А в прогрессировании рака яичников. Материал и методы. Исследовали образцы тканей от 76 больных эпителиальным раком яичников (серозная цистаденокарцинома: T1N0M0; T2N0M0; T3NxM0; T4Nx-1M0) и 47 больных цистаденомой. Гистологический контроль выполняли во всех случаях. В качестве условноинтактной ткани использовали яичники, удаленные во время оперативного вмешательства по поводу миомы матки (n = 20). Возраст больных составлял 50,9 ± 2,9 года. Методом иммуноферментного анализа со стандартными тест-системами определяли уровень ростовых факторов VEGF-A и его рецептора sVEGF-R1, VEGF-C и его рецептора sVEGF-R3. Результаты. Установлено, что по VEGF-А в цистаденомах не было достоверных различий с условноинтактными яичниками, а в ткани цистаденокарциномы его уровень возрастал на порядок на всех стадиях ее развития. Рецептор sVEGF-R1 относительно условноинтактной ткани яичника был снижен в цистаденоме, контралатеральном яичнике при T1N0M0 и пораженном яичнике при T4Nx-1M0. Уровень VEGF-С достоверно повышался в тканях всех новообразований, однако во всех стадиях цистаденокарциномы он был достоверно выше, чем в ткани цистаденомы. В контралатеральном яичнике при T1N0M0 его повышение оказалось на промежуточном уровне, достоверно отличаясь от всех остальных тканей. Растворимый рецептор sVEGF-R3 был достоверно повышен в поздних стадиях рака яичников T3NxM0 и T4Nx-1M0, понижен только в контралатеральном яичнике при T1N0M0, в остальных тканях не отличался от условноинтактных. Заключение. Результаты свидетельствуют о высокой активности образования лимфатических сосудов в доброкачественных опухолях и во всех стадиях развития злокачественных. Достоверное увеличение уровня VEGF-C в контралатеральном, не пораженном опухолью яичнике относительно ткани интактных яичников дает основание рассматривать VEGF-C наряду с VEGF-А в качестве патогенетического фактора развития новообразований яичников.</p></trans-abstract><kwd-group xml:lang="en"><kwd>VEGF family</kwd><kwd>cystadenoma</kwd><kwd>stages of the development of cystadenocarcinoma</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>семейство VEGF</kwd><kwd>цистаденома</kwd><kwd>стадии развития цистаденокарциномы</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Kathleen R.C., Ie-Ming S. Ovarian cancer. Annu. Rev. Pathol. 2009; (4): 287-313. DOI: 10.1146/annurev.pathol.4.110807.092246</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Lynch H.T., Casey M.J., Snyder C.L., Bewtra C., Lynch J.F., Butts M., Godwin A.K. Hereditary ovarian cancer: molecular genetics, pathology, management and heterogeneity. 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