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<article article-type="research-article" dtd-version="1.3" 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" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">mes</journal-id><journal-title-group><journal-title xml:lang="ru">Экстремальная биомедицина</journal-title><trans-title-group xml:lang="en"><trans-title>Extreme Medicine</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">3033-8964</issn><issn pub-type="epub">3033-8972</issn><publisher><publisher-name>Centre for Strategic Planning of the Federal Medical and Biological Agency</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.47183/mes.2021.044</article-id><article-id custom-type="elpub" pub-id-type="custom">mes-80</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОР</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEW</subject></subj-group></article-categories><title-group><article-title>Перспективы терапии рака молочной железы с использованием  онколитических вирусов</article-title><trans-title-group xml:lang="en"><trans-title>Recombinant adeno-associated viruses as a gene delivery vehicle for the use in molecular medicine</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Благов</surname><given-names>А. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Blagov</surname><given-names>A. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Александр Владимирович Благов,</p><p>д. 5, к. 6, ул. Щукинская, г. Москва, 123182. </p></bio><bio xml:lang="en"><p>Alexander V. Blagov,</p><p>5, k. 6, Shchukinskaya str., Moscow, 123182.</p></bio><email xlink:type="simple">ABlagov@cspfmba.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Центр стратегического планирования Федерального медико-биологического агентства</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Centre for Strategic Planning of the Federal Medical Biological Agency</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>24</day><month>10</month><year>2024</year></pub-date><volume>23</volume><issue>4</issue><fpage>34</fpage><lpage>41</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Благов А.В., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Благов А.В.</copyright-holder><copyright-holder xml:lang="en">Blagov A.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://www.extrememedicine.ru/jour/article/view/80">https://www.extrememedicine.ru/jour/article/view/80</self-uri><abstract><p>Рак молочной железы (РМЖ) — онкологическое заболевание с высокой распространенностью и смертностью среди женщин во всем мире. Диагностика РМЖ не столь эффективна для выявления заболевания на ранних стадиях, а терапевтические методы связаны с тяжелыми побочными эффектами. Онколитические вирусы могут стать новым эффективным средством в терапии РМЖ. Их эффективность обусловлена двумя типами воздействия на раковую опухоль: непосредственным уничтожением опухолевых клеток и запуском противоопухолевого иммунного ответа. Повысить эффективность терапии онколитическими вирусами можно путем конструирования генетически-модифицированных вирусов, обладающих лучшей селективностью к опухолевым клеткам молочной железы и (или) способных к большему усилению противоопухолевого иммунного ответа. Представлены дальнейшие направления применения онколитических вирусов в терапии РМЖ, оптимальные пути доставки вирусов в опухоль и эффективность их использования в комбинации с другими терапевтическими средствами (методами), а также перспектива использования онколитических вирусов в качестве противоопухолевых вакцин.</p></abstract><trans-abstract xml:lang="en"><p>Prospects of using oncolytic viruses in breast cancer therapy</p><p>Breast cancer (BC) is a cancer with a high prevalence and mortality among women worldwide.  With the current diagnostics methods, BC may remain undetected at its early stages, and the therapies developed for the disease are associated with severe side effects. Oncolytic viruses can be the basis of the new, effective BC treatment approaches. The viruses destroy tumor cells directly and launch the antitumor immune response; this dual action supports their efficacy. It is possible to make the oncolytic virus therapy more effective by designing genetically modified viruses that can target BC cells better and/or induce a stronger antitumor immune response. This review outlines the directions of development of oncolytic viruses in BC treatment, covers the optimal ways of delivering viruses to the tumor and the efficacy of their use in combination with other therapeutic agents (methods) and presents the prospects of using oncolytic viruses in antitumor vaccines.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>онколитические вирусы</kwd><kwd>рак молочной железы</kwd><kwd>вирусный вектор</kwd><kwd>химиотерапия</kwd><kwd>эстрогеновые рецепторы</kwd></kwd-group><kwd-group xml:lang="en"><kwd>oncolytic viruses</kwd><kwd>breast cancer</kwd><kwd>viral vector</kwd><kwd>chemotherapy</kwd><kwd>estrogen receptors</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Shah R, Rosso K, Nathanson SD. Pathogenesis, prevention, diagnosis and treatment of breast cancer. World J Clin Oncol. 2014; 5 (3): 283–98. DOI: 10.5306/wjco.v5.i3.283.</mixed-citation><mixed-citation xml:lang="en">Shah R, Rosso K, Nathanson SD. Pathogenesis, prevention, diagnosis and treatment of breast cancer. World J Clin Oncol. 2014; 5 (3): 283–98. DOI: 10.5306/wjco.v5.i3.283.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Государственное казенное учреждение здравоохранения Пермского края «Пермский краевой центр по профилактике и борьбе со СПИД и инфекционными заболеваниями». Всемирный День борьбы с РМЖ (дата обращения 14.06.2021). Доступно по ссылке: www.aids-centr.perm.ru/Новости-центра/Всемирный-День-борьбы-с-раком-молочнойжелезы234234234234234234234.</mixed-citation><mixed-citation xml:lang="en">Gosudarstvennoe kazennoe uchrezhdenie zdravoohranenija Permskogo kraja «Permskij kraevoj centr po profilaktike i bor'be so SPID i infekcionnymi zabolevanijami». Vsemirnyj Den' bor'by s RMZh (data obrashhenija 14.06.2021). Dostupno po ssylke: www.aidscentr.perm.ru/Новости-центра/Всемирный-День-борьбы-сраком-молочной-железы234234234234234234234. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Feng Y, Spezia M, Huang S, et al. Breast cancer development and progression: Risk factors, cancer stem cells, signaling pathways, genomics, and molecular pathogenesis. Genes Dis. 2018; 5 (2): 77–106. DOI: 10.1016/j.gendis.2018.05.001.</mixed-citation><mixed-citation xml:lang="en">Feng Y, Spezia M, Huang S, et al. Breast cancer development and progression: Risk factors, cancer stem cells, signaling pathways, genomics, and molecular pathogenesis. Genes Dis. 2018; 5 (2): 77–106. DOI: 10.1016/j.gendis.2018.05.001.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Всемирная организация здравоохранения. Рак (дата обращения 15.06.2021). Доступно по ссылке: www.who.int/ru/news-room/fact-sheets/detail/cancer.</mixed-citation><mixed-citation xml:lang="en">Vsemirnaja organizacija zdravoohranenija. Rak (data obrashhenija 15.06.2021). Dostupno po ssylke: www.who.int/ru/news-room/fact-sheets/detail/cancer. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Treating Breast Cancer. (date views 15.06.2021). Available from: www.cancer.org/cancer/breast-cancer/treatment.html.</mixed-citation><mixed-citation xml:lang="en">Treating Breast Cancer (date views 15.06.2021). Available from: www.cancer.org/cancer/breast-cancer/treatment.html.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Radiation for Breast Cancer (date views 15.06.2021). Available from: www.cancer.org/cancer/breast-cancer/treatment/radiationfor-breast-cancer.html.</mixed-citation><mixed-citation xml:lang="en">Radiation for Breast Cancer (date views 15.06.2021). Available from: www.cancer.org/cancer/breast-cancer/treatment/radiationfor-breast-cancer.html.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Collins KK, Liu Y, Schootman M, et al. Effects of breast cancer surgery and surgical side effects on body image over time. Breast Cancer Res Treat. 2011; 126 (1): 167–76. DOI: 10.1007/s10549010-1077-7.</mixed-citation><mixed-citation xml:lang="en">Collins KK, Liu Y, Schootman M, et al. Effects of breast cancer surgery and surgical side effects on body image over time. Breast Cancer Res Treat. 2011; 126 (1): 167–76. DOI: 10.1007/s10549010-1077-7.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Chemotherapy Side Effects (date views 15.06.2021). Available from: www.cancer.org/treatment/treatments-and-side-effects/treatment-types/chemotherapy/chemotherapy-side-effects.html.</mixed-citation><mixed-citation xml:lang="en">Chemotherapy Side Effects (date views 15.06.2021). Available from: www.cancer.org/treatment/treatments-and-side-effects/treatment-types/chemotherapy/chemotherapy-side-effects.html.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Evgin L, Vile RG. Parking CAR T Cells in Tumours: Oncolytic Viruses as Valets or Vandals? Cancers (Basel). 2021; 13 (5): 1106. DOI: 10.3390/cancers13051106.</mixed-citation><mixed-citation xml:lang="en">Evgin L, Vile RG. Parking CAR T Cells in Tumours: Oncolytic Viruses as Valets or Vandals? Cancers (Basel). 2021; 13 (5): 1106. DOI: 10.3390/cancers13051106.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Feng Y, Spezia M, Huang S, et al. Breast cancer development and progression: Risk factors, cancer stem cells, signaling pathways, genomics, and molecular pathogenesis. Genes Dis. 2018; 5 (2): 77–106. DOI: 10.1016/j.gendis.2018.05.001.</mixed-citation><mixed-citation xml:lang="en">Feng Y, Spezia M, Huang S, et al. Breast cancer development and progression: Risk factors, cancer stem cells, signaling pathways, genomics, and molecular pathogenesis. Genes Dis. 2018; 5 (2): 77–106. DOI: 10.1016/j.gendis.2018.05.001.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Клинические рекомендации. Рак молочной железы. П.1.5. 2021. Министерство здравоохранения Российской Федерации.</mixed-citation><mixed-citation xml:lang="en">Klinicheskie rekomendacii. Rak molochnoj zhelezy. P.1.5. 2021. Ministerstvo zdravoohranenija Rossijskoj Federacii. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Fallahpour S, Navaneelan T, De P, Borgo A. Breast cancer survival by molecular subtype: a population-based analysis of cancer registry data. CMAJ Open. 2017; 5 (3): E734–E739. DOI: 10.9778/cmajo.20170030.</mixed-citation><mixed-citation xml:lang="en">Fallahpour S, Navaneelan T, De P, Borgo A. Breast cancer survival by molecular subtype: a population-based analysis of cancer registry data. CMAJ Open. 2017; 5 (3): E734–E739. DOI: 10.9778/cmajo.20170030.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Howlader N, Cronin KA, Kurian AW, Andridge R. Differences in Breast Cancer Survival by Molecular Subtypes in the United States. Cancer Epidemiol Biomarkers Prev. 2018; 27 (6): 619–26. DOI: 10.1158/1055-9965.EPI-17-0627.</mixed-citation><mixed-citation xml:lang="en">Howlader N, Cronin KA, Kurian AW, Andridge R. Differences in Breast Cancer Survival by Molecular Subtypes in the United States. Cancer Epidemiol Biomarkers Prev. 2018; 27 (6): 619–26. DOI: 10.1158/1055-9965.EPI-17-0627.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Al-Thoubaity FK. Molecular classification of breast cancer: A retrospective cohort study. Ann Med Surg. 2019; 49: 44–48. DOI: 10.1016/j.amsu.2019.11.021.</mixed-citation><mixed-citation xml:lang="en">Al-Thoubaity FK. Molecular classification of breast cancer: A retrospective cohort study. Ann Med Surg. 2019; 49: 44–48. DOI: 10.1016/j.amsu.2019.11.021.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Brufsky AM, Dickler MN. Estrogen Receptor-Positive Breast Cancer: Exploiting Signaling Pathways Implicated in Endocrine Resistance. Oncologist. 2018; 23 (5): 528–39. DOI: 10.1634/ theoncologist.2017-0423.</mixed-citation><mixed-citation xml:lang="en">Brufsky AM, Dickler MN. Estrogen Receptor-Positive Breast Cancer: Exploiting Signaling Pathways Implicated in Endocrine Resistance. Oncologist. 2018; 23 (5): 528–39. DOI: 10.1634/theoncologist.2017-0423.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Wee P, Wang Z. Epidermal Growth Factor Receptor Cell Proliferation Signaling Pathways. Cancers. 2017; 9 (5): 52. DOI: 10.3390/cancers9050052.</mixed-citation><mixed-citation xml:lang="en">Wee P, Wang Z. Epidermal Growth Factor Receptor Cell Proliferation Signaling Pathways. Cancers. 2017; 9 (5): 52. DOI: 10.3390/cancers9050052.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Corrigan PA, Beaulieu C, Patel RB, Lowe DK. Talimogene Laherparepvec: An Oncolytic Virus Therapy for Melanoma. Ann Pharmacother. 2017; 51 (8): 675–81. DOI: 10.1177/1060028017702654.</mixed-citation><mixed-citation xml:lang="en">Corrigan PA, Beaulieu C, Patel RB, Lowe DK. Talimogene Laherparepvec: An Oncolytic Virus Therapy for Melanoma. Ann Pharmacother. 2017; 51 (8): 675–81. DOI: 10.1177/1060028017702654.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">12 Studies found for: oncolytic viruses. Breast Cancer. Available from: https://clinicaltrials.gov/ct2/results?cond=Breast+Cancer&amp;term=oncolytic+viruses&amp;cntry=&amp;state=&amp;city=&amp;dist= (дата обращения: 10.09.2021).</mixed-citation><mixed-citation xml:lang="en">12 Studies found for: oncolytic viruses. Breast Cancer. Available from: https://clinicaltrials.gov/ct2/results?cond=Breast+Cancer&amp;term=oncolytic+viruses&amp;cntry=&amp;state=&amp;city=&amp;dist= (data obrashhenija: 10.09.2021).</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Chiocca EA, Rabkin SD. Oncolytic viruses and their application to cancer immunotherapy [published correction appears in Cancer Immunol Res. 2014; 2 (7): 699] Cancer Immunol Res. 2014; 2 (4): 295–300. DOI: 10.1158/2326-6066.CIR-14-0015.</mixed-citation><mixed-citation xml:lang="en">Chiocca EA, Rabkin SD. Oncolytic viruses and their application to cancer immunotherapy [published correction appears in Cancer Immunol Res. 2014; 2 (7): 699] Cancer Immunol Res. 2014; 2 (4): 295–300. DOI: 10.1158/2326-6066.CIR-14-0015.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">O Bryan SM, Mathis JM. Oncolytic Virotherapy for Breast Cancer Treatment. Curr Gene Ther. 2018; 18 (4): 192–205. DOI: 10.2174/1566523218666180910163805.</mixed-citation><mixed-citation xml:lang="en">O Bryan SM, Mathis JM. Oncolytic Virotherapy for Breast Cancer Treatment. Curr Gene Ther. 2018; 18 (4): 192–205. DOI: 10.2174/1566523218666180910163805.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Lawler SE, Speranza MC, Cho CF, Chiocca EA. Oncolytic viruses in cancer treatment: a review. JAMA Oncol. 2017; 3 (6): 841–9. DOI: 10.1001/jamaoncol.2016.2064.</mixed-citation><mixed-citation xml:lang="en">Lawler SE, Speranza MC, Cho CF, Chiocca EA. Oncolytic viruses in cancer treatment: a review. JAMA Oncol. 2017; 3 (6): 841–9. DOI: 10.1001/jamaoncol.2016.2064.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Nakashima H, Kaur B, Chiocca EA. Directing systemic oncolytic viral delivery to tumors via carrier cells. Cytokine Growth Factor Rev. 2010; 21 (2–3): 119–26. DOI: 10.1016/j.cytogfr.2010.02.004.</mixed-citation><mixed-citation xml:lang="en">Nakashima H, Kaur B, Chiocca EA. Directing systemic oncolytic viral delivery to tumors via carrier cells. Cytokine Growth Factor Rev. 2010; 21 (2–3): 119–26. DOI: 10.1016/j.cytogfr.2010.02.004.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Russell SJ, Peng KW, Bell JC. Oncolytic virotherapy. Nat Biotechnol. 2012; 30 (7): 658–70. DOI: 10.1038/nbt.2287.</mixed-citation><mixed-citation xml:lang="en">Russell SJ, Peng KW, Bell JC. Oncolytic virotherapy. Nat Biotechnol. 2012; 30 (7): 658–70. DOI: 10.1038/nbt.2287.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Kretschmer M, Kadlubowska P, Hoffmann D, Schwalbe B, Auerswald H, Schreiber M. Zikavirus prME Envelope Pseudotyped Human Immunodeficiency Virus Type-1 as a Novel Tool for Glioblastoma-Directed Virotherapy. Cancers. 2020; 12 (4): 1000. DOI: 10.3390/cancers12041000.</mixed-citation><mixed-citation xml:lang="en">Kretschmer M, Kadlubowska P, Hoffmann D, Schwalbe B, Auerswald H, Schreiber M. Zikavirus prME Envelope Pseudotyped Human Immunodeficiency Virus Type-1 as a Novel Tool for Glioblastoma-Directed Virotherapy. Cancers. 2020; 12 (4): 1000. DOI: 10.3390/cancers12041000.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Melcher A, Parato K, Rooney CM, Bell JC. Thunder and lightning: immunotherapy and oncolytic viruses collide. Mol Ther. 2011; 19 (6): 1008–16. DOI: 10.1038/mt.2011.65.</mixed-citation><mixed-citation xml:lang="en">Melcher A, Parato K, Rooney CM, Bell JC. Thunder and lightning: immunotherapy and oncolytic viruses collide. Mol Ther. 2011; 19 (6): 1008–16. DOI: 10.1038/mt.2011.65.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Chaurasiya S, Fong Y. Viroimmunotherapy for breast cancer: promises, problems and future directions [published online ahead of print, 2020 Dec 2]. Cancer Gene Ther. 2020; DOI: 10.1038/s41417-020-00265-6.</mixed-citation><mixed-citation xml:lang="en">Chaurasiya S, Fong Y. Viroimmunotherapy for breast cancer: promises, problems and future directions [published online ahead of print, 2020 Dec 2] Cancer Gene Ther. 2020; DOI: 10.1038/ s41417-020-00265-6.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Bauerschmitz GJ, Ranki T, Kangasniemi L, Ribacka C, Eriksson M, Porten M, et al. Tissue-specific promoters active in CD44+CD24–/ low breast cancer cells. Cancer Res. 2008; 68: 5533–9.</mixed-citation><mixed-citation xml:lang="en">Bauerschmitz GJ, Ranki T, Kangasniemi L, Ribacka C, Eriksson M, Porten M, et al. Tissue-specific promoters active in CD44+CD24–/ low breast cancer cells. Cancer Res. 2008; 68: 5533–9.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Xu W, Yang Y, Hu Z, Head M, Mangold KA, Sullivan M, et al. LyP1-modified oncolytic adenoviruses targeting transforming growth factor beta inhibit tumor growth and metastases and augment immune checkpoint inhibitor therapy in breast cancer mouse models. Hum Gene Ther. 2020; 31: 15–6.</mixed-citation><mixed-citation xml:lang="en">Xu W, Yang Y, Hu Z, Head M, Mangold KA, Sullivan M, et al. LyP1-modified oncolytic adenoviruses targeting transforming growth factor beta inhibit tumor growth and metastases and augment immune checkpoint inhibitor therapy in breast cancer mouse models. Hum Gene Ther. 2020; 31: 15–6.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Menotti L, Cerretani A, Hengel H, Campadelli-Fiume G. Construction of a fully retargeted herpes simplex virus 1 recombinant capable of entering cells solely via human epidermal growth factor receptor 2. J Virol. 2008; 82: 10153–61.</mixed-citation><mixed-citation xml:lang="en">Menotti L, Cerretani A, Hengel H, Campadelli-Fiume G. Construction of a fully retargeted herpes simplex virus 1 recombinant capable of entering cells solely via human epidermal growth factor receptor 2. J Virol. 2008; 82: 10153–61.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Shayestehpour M, Moghim S, Salimi V, et al. Targeting human breast cancer cells by an oncolytic adenovirus using microRNAtargeting strategy. Virus Res. 2017; 240: 207–14. DOI: 10.1016/j.virusres.2017.08.016.</mixed-citation><mixed-citation xml:lang="en">Shayestehpour M, Moghim S, Salimi V, et al. Targeting human breast cancer cells by an oncolytic adenovirus using microRNAtargeting strategy. Virus Res. 2017; 240: 207–14. DOI: 10.1016/j.virusres.2017.08.016.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Platonov ME, Borovjagin AV, Kaverina N, et al. KISS1 tumor suppressor restricts angiogenesis of breast cancer brain metastases and sensitizes them to oncolytic virotherapy in vitro. Cancer Lett. 2018; 417: 75–88. DOI: 10.1016/j.canlet.2017.12.024.</mixed-citation><mixed-citation xml:lang="en">Platonov ME, Borovjagin AV, Kaverina N, et al. KISS1 tumor suppressor restricts angiogenesis of breast cancer brain metastases and sensitizes them to oncolytic virotherapy in vitro. Cancer Lett. 2018; 417: 75–88. DOI: 10.1016/j.canlet.2017.12.024.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Mohamed Amin Z, Ani MAC, Tan SW, et al. Evaluation of a recombinant newcastle disease virus expressing human IL12 against human breast cancer. Sci Rep. 2019; 9 (1): 1–10. Available from: https://doi.org/10.1038/s41598-019-50222-z.</mixed-citation><mixed-citation xml:lang="en">Mohamed Amin Z, Ani MAC, Tan SW, et al. Evaluation of a recombinant newcastle disease virus expressing human IL12 against human breast cancer. Sci Rep. 2019; 9 (1): 1–10. Available from: https://doi.org/10.1038/s41598-019-50222-z.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Yan Y, Xu H, Wang J, et al. Inhibition of breast cancer cells by targeting E2F-1 gene and expressing IL15 oncolytic adenovirus Biosci Rep. 2019; 39 (7). Available from: https://doi.org/10.1042/BSR20190384.</mixed-citation><mixed-citation xml:lang="en">Yan Y, Xu H, Wang J, et al. Inhibition of breast cancer cells by targeting E2F-1 gene and expressing IL15 oncolytic adenovirus Biosci Rep. 2019; 39 (7). Available from: https://doi.org/10.1042/BSR20190384.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Chon HJ, Lee WS, Yang H, Kong SJ, Lee NK, Moon ES, et al. Tumor microenvironment remodeling by intratumoral oncolytic vaccinia virus enhances the efficacy of immune-checkpoint blockade. Clin Cancer Res. 2019; 25: 1612–23.</mixed-citation><mixed-citation xml:lang="en">Chon HJ, Lee WS, Yang H, Kong SJ, Lee NK, Moon ES, et al. Tumor microenvironment remodeling by intratumoral oncolytic vaccinia virus enhances the efficacy of immune-checkpoint blockade. Clin Cancer Res. 2019; 25: 1612–23.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Liikanen I, Tähtinen S, Guse K, et al. Oncolytic Adenovirus Expressing Monoclonal Antibody Trastuzumab for Treatment of HER2-Positive Cancer. Mol Cancer Ther. 2016; 15 (9): 2259–69. DOI: 10.1158/1535-7163.MCT-15-0819.</mixed-citation><mixed-citation xml:lang="en">Liikanen I, Tähtinen S, Guse K, et al. Oncolytic Adenovirus Expressing Monoclonal Antibody Trastuzumab for Treatment of HER2-Positive Cancer. Mol Cancer Ther. 2016; 15 (9): 2259–69. DOI: 10.1158/1535-7163.MCT-15-0819.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Gholami S, Marano A, Chen NG, Aguilar RJ, Frentzen A, Chen CH, et al. A novel vaccinia virus with dual oncolytic and anti-angiogenic therapeutic effects against triple-negative breast cancer. Breast Cancer Res Treat. 2014; 148: 489–99.</mixed-citation><mixed-citation xml:lang="en">Gholami S, Marano A, Chen NG, Aguilar RJ, Frentzen A, Chen CH, et al. A novel vaccinia virus with dual oncolytic and anti-angiogenic therapeutic effects against triple-negative breast cancer. Breast Cancer Res Treat. 2014; 148: 489–99.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Martini V, D'Avanzo F, Maggiora PM, Varughese FM, Sica A, Gennari A. Oncolytic virotherapy: new weapon for breast cancer treatment. E Cancer Medicals Science. 2020; 14: 1149. DOI: 10.3332/ecancer.2020.1149.</mixed-citation><mixed-citation xml:lang="en">Martini V, D'Avanzo F, Maggiora PM, Varughese FM, Sica A, Gennari A. Oncolytic virotherapy: new weapon for breast cancer treatment. E Cancer Medicals Science. 2020; 14: 1149. DOI: 10.3332/ecancer.2020.1149.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Iankov ID, Msaouel P, Allen C, et al. Demonstration of anti-tumor activity of oncolytic measles virus strains in a malignant pleural effusion breast cancer model. Breast Cancer Res Treat. 2010; 122 (3): 745–54. DOI: 10.1007/s10549-009-0602-z.</mixed-citation><mixed-citation xml:lang="en">Iankov ID, Msaouel P, Allen C, et al. Demonstration of anti-tumor activity of oncolytic measles virus strains in a malignant pleural effusion breast cancer model. Breast Cancer Res Treat. 2010; 122 (3): 745–54. DOI: 10.1007/s10549-009-0602-z.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">McGray AJR, Huang RY, Battaglia S, Eppolito C, Miliotto A, Stephenson KB, et al. Oncolytic Maraba virus armed with tumor antigen boosts vaccine priming and reveals diverse therapeutic response patterns when combined with checkpoint blockade in ovarian cancer. J Immunother Cancer. 2019; 7: 189.</mixed-citation><mixed-citation xml:lang="en">McGray AJR, Huang RY, Battaglia S, Eppolito C, Miliotto A, Stephenson KB, et al. Oncolytic Maraba virus armed with tumor antigen boosts vaccine priming and reveals diverse therapeutic response patterns when combined with checkpoint blockade in ovarian cancer. J Immunother Cancer. 2019; 7: 189.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Kwan A, Winder N, Muthana M. Oncolytic Virotherapy Treatment of Breast Cancer: Barriers and Recent Advances. Viruses. 2021; 13 (6): 1128. DOI: 10.3390/v13061128.</mixed-citation><mixed-citation xml:lang="en">Kwan A, Winder N, Muthana M. Oncolytic Virotherapy Treatment of Breast Cancer: Barriers and Recent Advances. Viruses. 2021; 13 (6): 1128. DOI: 10.3390/v13061128.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Bourgeois-Daigneault MC, St-Germain LE, Roy DG, et al. Combination of Paclitaxel and MG1 oncolytic virus as a successful strategy for breast cancer treatment. Breast Cancer Res. 2016; 18 (1): 83. DOI: 10.1186/s13058-016-0744-y.</mixed-citation><mixed-citation xml:lang="en">Bourgeois-Daigneault MC, St-Germain LE, Roy DG, et al. Combination of Paclitaxel and MG1 oncolytic virus as a successful strategy for breast cancer treatment. Breast Cancer Res. 2016; 18 (1): 83. DOI: 10.1186/s13058-016-0744-y.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Bernstein V, Ellard SL, Dent SF, et al. A randomized phase II study of weekly paclitaxel with or without pelareorep in patients with metastatic breast cancer: final analysis of Canadian Cancer Trials Group IND.213. Breast Cancer Res Treat. 2018; 167 (2): 485–93. DOI: 10.1007/s10549-017-4538-4.</mixed-citation><mixed-citation xml:lang="en">Bernstein V, Ellard SL, Dent SF, et al. A randomized phase II study of weekly paclitaxel with or without pelareorep in patients with metastatic breast cancer: final analysis of Canadian Cancer Trials Group IND.213. Breast Cancer Res Treat. 2018; 167 (2): 485–93. DOI: 10.1007/s10549-017-4538-4.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Wang S, Jhawar S, Bommareddy P, Thandoni A, Aspromonte S, Pepe R, et al. Combined radiation and oncolytic viral therapy augments cytotoxic and immunogenic antitumor effects against melanoma. Int J Radiat Oncol. 2018; 102: S153–S154. DOI: 10.1016/j.ijrobp.2018.06.371.</mixed-citation><mixed-citation xml:lang="en">Wang S, Jhawar S, Bommareddy P, Thandoni A, Aspromonte S, Pepe R, et al. Combined radiation and oncolytic viral therapy augments cytotoxic and immunogenic antitumor effects against melanoma. Int J Radiat Oncol. 2018; 102: S153–S154. DOI: 10.1016/j.ijrobp.2018.06.371.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">O'Cathail SM, Pokrovska TD, Maughan TS, Fisher KD, Seymour LW, Hawkins MA. Combining Oncolytic Adenovirus with Radiation-A Paradigm for the Future of Radiosensitization. Front Oncol. 2017; 7: 153. DOI: 10.3389/fonc.2017.00153.</mixed-citation><mixed-citation xml:lang="en">O'Cathail SM, Pokrovska TD, Maughan TS, Fisher KD, Seymour LW, Hawkins MA. Combining Oncolytic Adenovirus with Radiation-A Paradigm for the Future of Radiosensitization. Front Oncol. 2017; 7: 153. DOI: 10.3389/fonc.2017.00153.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Chung V, Kos FJ, Hardwick N, et al. Evaluation of safety and efficacy of p53MVA vaccine combined with pembrolizumab in patients with advanced solid cancers. Clin Transl Oncol. 2019; 21 (3): 363–72. DOI: 10.1007/s12094-018-1932-2.</mixed-citation><mixed-citation xml:lang="en">Chung V, Kos FJ, Hardwick N, et al. Evaluation of safety and efficacy of p53MVA vaccine combined with pembrolizumab in patients with advanced solid cancers. Clin Transl Oncol. 2019; 21 (3): 363–72. DOI: 10.1007/s12094-018-1932-2.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Kelly CM, Antonescu CR, Bowler T, et al. Objective response rate among patients with locally advanced or metastatic sarcoma treated with talimogene laherparepvec in combination with pembrolizumab: a phase 2 clinical trial. JAMA Oncol. 2020; 6 (3): 402–8. DOI: 10.1001/jamaoncol.2019.6152.</mixed-citation><mixed-citation xml:lang="en">Kelly CM, Antonescu CR, Bowler T, et al. Objective response rate among patients with locally advanced or metastatic sarcoma treated with talimogene laherparepvec in combination with pembrolizumab: a phase 2 clinical trial. JAMA Oncol. 2020; 6 (3): 402–8. DOI: 10.1001/jamaoncol.2019.6152.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
