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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="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Infection and Immunity</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Infection and Immunity</journal-title><trans-title-group xml:lang="ru"><trans-title>Инфекция и иммунитет</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2220-7619</issn><issn publication-format="electronic">2313-7398</issn><publisher><publisher-name xml:lang="en">SPb RAACI</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">17585</article-id><article-id pub-id-type="doi">10.15789/2220-7619-TRO-17585</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">The role of RNA viruses in human cancers</article-title><trans-title-group xml:lang="ru"><trans-title>Роль РНК-вирусов в онкогенезе человека</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Fazlalipour</surname><given-names>M.</given-names></name><name xml:lang="ru"><surname>Фазлалипур</surname><given-names>М.</given-names></name></name-alternatives><address><country country="IR">Iran, Islamic Republic of</country></address><bio xml:lang="en"><p>PhD in Virology; PhD in Virology; Assistant Professor, WHO Collaborating Center for Reference and Research on Rabies; Assistant Professor, Research Center for Emerging and Reemerging Infectious Diseases</p></bio><bio xml:lang="ru"><p>кандидат наук по вирусологии, ассистент, Сотрудничающего центра ВОЗ по стандартам и исследованиям бешенства; ассистент Исследовательского центра новых и вновь возникающих инфекционных заболеваний</p></bio><email>mfp.virology@gmail.com</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Mollaei</surname><given-names>H.R.</given-names></name><name xml:lang="ru"><surname>Моллаи</surname><given-names>Х.Р.</given-names></name></name-alternatives><address><country country="IR">Iran, Islamic Republic of</country></address><bio xml:lang="en"><p>PhD in Virology; Assistant Professor</p></bio><bio xml:lang="ru"><p>кандидат наук по вирусологии, ассистент</p></bio><email>mfp.virology@gmail.com</email><xref ref-type="aff" rid="aff2"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Pasteur Institute of Iran</institution></aff><aff><institution xml:lang="ru">Институт Пастера Ирана</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">Kerman University of Medical Sciences</institution></aff><aff><institution xml:lang="ru">Керманский университет медицинских наук</institution></aff></aff-alternatives><pub-date date-type="preprint" iso-8601-date="2024-05-28" publication-format="electronic"><day>28</day><month>05</month><year>2024</year></pub-date><pub-date date-type="pub" iso-8601-date="2024-06-05" publication-format="electronic"><day>05</day><month>06</month><year>2024</year></pub-date><volume>14</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>209</fpage><lpage>226</lpage><history><date date-type="received" iso-8601-date="2024-01-31"><day>31</day><month>01</month><year>2024</year></date><date date-type="accepted" iso-8601-date="2024-05-14"><day>14</day><month>05</month><year>2024</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, Fazlalipour M., Mollaei H.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, Фазлалипур М., Моллаи Х.</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">Fazlalipour M., Mollaei H.</copyright-holder><copyright-holder xml:lang="ru">Фазлалипур М., Моллаи Х.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://iimmun.ru/iimm/article/view/17585">https://iimmun.ru/iimm/article/view/17585</self-uri><abstract xml:lang="en"><p>Many RNA viruses have been reported to be oncogenic (or carcinogenic) in a variety of animal and human cancers. The increase in the incidence and prevalence of cancer-causing viruses in human populations can be known as a key precursor to the development of various cancers. The retrovirus family and Hepatitis C virus (HCV) are also reported to cause cancer. Viral oncoproteins such as Tax of HTLV 1 interacts with cellular ubiquitination complex such as cyclindromatosis tumor suppressor, ubiquitin-specific proteases 7, 11, 15 and 20, A-20 and signal-transducing adaptor molecule binding protein-like-1 in order to improve the cellular signaling pathways. The viral oncoproteins binding to DUB, leading to proliferation of virus-infected cells and cell transformation. Proto-oncogenes (c-onc genes) are the cellular form of v-onc genes. The activation of c-onc genes leads to cell growth. C-onc genes are transformed into an oncogenic form by viral infection. C-onc genes play some roles such as protein kinases, growth factors, growth factor receptors, and DNA binding proteins. The study of transforming retroviruses and their oncogenes and the multiple mechanisms deployed by other RNA viruses to use the growth-suppressive and proapoptotic function of tumor suppressor genes has been added to our current understanding of cancer biology. Oncogenic RNA viruses are important experimental models to study molecular investigation such as cellular networks, including the discovery of oncogenes and tumor suppressors. Understanding of different strategies of RNA viruses as well as the function of their proteins helps to make more extensive plans regarding the adoption of follow-up, prevention and treatment strategies in cancer patients caused by viral origin.</p></abstract><trans-abstract xml:lang="ru"><p>Известно, что многие РНК-вирусы являются онкогенными (или канцерогенными) при различных видах рака у животных и человека. Увеличение заболеваемости и распространенности вирусов, вызывающих рак, в человеческой популяции можно расценивать как ключевой предшественник развития различных видов рака. Семейство ретровирусов и вирус гепатита С (ВГС) также вызывают рак. Вирусные онкопротеины, такие как Tax Т-лимфотропного вируса человека (HTLV-1), взаимодействуют с клеточным комплексом убиквитинирования, таким как супрессор опухоли цилиндроматоза, убиквитин-специфические протеазы 7, 11, 15 и 20, А-20 и STAMBPL1 для усиления клеточных сигнальных путей. Вирусные онкопротеины связываются с деубиквитиназой, что приводит к пролиферации инфицированных клеток и клеточной трансформации. Протоонкогены (гены c-onc) представляют собой клеточную форму генов v-onc. Активация генов c-onc приводит к росту клеток. Гены с-onc трансформируются в онкогенную форму при вирусной инфекции могут выступать в качестве протеинкиназ, факторов роста, рецепторов факторов роста и ДНК-связывающих белков. Изучение трансформирующих ретровирусов и их онкогенов, а также разных механизмов, используемых другими РНК-вирусами для подавления роста и проапоптотической функции генов-супрессоров опухолей привносит новые данные в понимание биологии рака. Онкогенные РНК-вирусы являются важными экспериментальными молекулярными моделями по изучению клеточных сетей, включая открытие онкогенов и супрессоров опухолей. Понимание различных стратегий РНК-вирусов, а также функций их белков помогает расширить стратегии для последующего наблюдения, профилактики и лечения больных раком, обусловленного различными вирусами.</p></trans-abstract><kwd-group xml:lang="en"><kwd>RNA virus</kwd><kwd>cancer</kwd><kwd>oncogenesis</kwd><kwd>tumor</kwd><kwd>carcinogen</kwd><kwd>Iran</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>РНК-вирус</kwd><kwd>рак</kwd><kwd>онкогенез</kwd><kwd>опухоль</kwd><kwd>канцероген</kwd><kwd>Иран</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Ajiro M., Zheng Z.M. Oncogenes and RNA splicing of human tumor viruses. Emerg. Microbes Infect., 2014, vol. 3, no. 9: e63. doi: 10.1038/emi.2014.62</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Alibek K., Kakpenova A., Mussabekova A., Sypabekova M., Karatayeva N. Role of viruses in the development of breast cancer. Infect. 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