<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.3 20210610//EN" "JATS-journalpublishing1-3.dtd">
<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">ldt</journal-id><journal-title-group><journal-title xml:lang="ru">Лучевая диагностика и терапия</journal-title><trans-title-group xml:lang="en"><trans-title>Diagnostic radiology and radiotherapy</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2079-5343</issn><publisher><publisher-name>Baltic Medical Education Center</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.22328/2079-5343-2023-14-2-15-30</article-id><article-id custom-type="elpub" pub-id-type="custom">ldt-875</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>ЛЕКЦИИ И ОБЗОРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>LECTURES AND REVIEWS</subject></subj-group></article-categories><title-group><article-title>Тераностика трижды негативного рака молочной железы: обзор</article-title><trans-title-group xml:lang="en"><trans-title>Theranostics of triple negative breast cancer: a review</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-3882-1720</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Молчанов</surname><given-names>О. Е.</given-names></name><name name-style="western" xml:lang="en"><surname>Molchanov</surname><given-names>O. E.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Молчанов Олег Евгеньевич — доктор медицинских наук, руководитель отдела фундаментальных исследований </p><p>197758, Санкт-Петербург, пос. Песочный, Ленинградская ул., д. 70</p></bio><bio xml:lang="en"><p>Oleg E. Molchanov — Dr. of Sci. (Med.), Head of the Department of Fundamental Research </p><p>St. Petersburg. Pos. Pesochny, Leningradskaya st. 70</p></bio><email xlink:type="simple">molchanovo@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8174-7461</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Майстренко</surname><given-names>Д. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Maystrenko</surname><given-names>D. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Майстренко Дмитрий Николаевич — доктор медицинских наук, директор</p><p>197758, Санкт-Петербург, пос. Песочный, Ленинградская ул., д. 70</p></bio><bio xml:lang="en"><p>Dmitry N. Maystrenko — Dr. of Sci (Med.), Head</p><p>St. Petersburg. Pos. Pesochny, Leningradskaya st. 70</p></bio><email xlink:type="simple">may64@inbox.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1630-0564</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Станжевский</surname><given-names>А. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Stanzhevskii</surname><given-names>A. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Станжевский Андрей Алексеевич — доктор медицинских наук, заместитель директора по научной работе</p><p>197758, Санкт-Петербург, пос. Песочный, Ленинградская ул., д. 70</p></bio><bio xml:lang="en"><p>Andrei A. Stanzhevskii — Dr. of Sci (Med.), Deputy Director for Research</p><p>St. Petersburg. Pos. Pesochny, Leningradskaya st. 70</p></bio><email xlink:type="simple">fakstanzhevsky@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Российский научный центр радиологии и хирургических технологий имени академика А.М. Гранова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>A.M.Granov Russian Research Centre for Radiology and Surgical Technologies</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2023</year></pub-date><pub-date pub-type="epub"><day>05</day><month>07</month><year>2023</year></pub-date><volume>14</volume><issue>2</issue><fpage>15</fpage><lpage>30</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Молчанов О.Е., Майстренко Д.Н., Станжевский А.А., 2023</copyright-statement><copyright-year>2023</copyright-year><copyright-holder xml:lang="ru">Молчанов О.Е., Майстренко Д.Н., Станжевский А.А.</copyright-holder><copyright-holder xml:lang="en">Molchanov O.E., Maystrenko D.N., Stanzhevskii A.A.</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://radiag.bmoc-spb.ru/jour/article/view/875">https://radiag.bmoc-spb.ru/jour/article/view/875</self-uri><abstract><sec><title>ВВЕДЕНИЕ</title><p>ВВЕДЕНИЕ: Трижды негативный рак является одним из наиболее агрессивных вариантов опухоли молочной железы. В настоящее время не предложено эффективных методов лечения, которые позволяли бы существенно повлиять на отдаленные результаты лечения.</p></sec><sec><title>ЦЕЛЬ</title><p>ЦЕЛЬ: Обобщить возможности тераностики и нанотераностики в визуализации и элиминации злокачественных клеток и иммуносупрессивных компонентов микроокружения трижды негативного рака молочной железы.</p></sec><sec><title>МАТЕРИАЛЫ И МЕТОДЫ</title><p>МАТЕРИАЛЫ И МЕТОДЫ: Проведен поиск научных публикаций в информационно-аналитической системе PubMed за 2015–2022 гг. по ключевым словам: «triple negative breast cancer» («трижды негативный рак молочной железы), «signaling pathways» («сигнальные пути»), «tumor microenvironment» («микроокружение опухоли»), «cancer stem cells» («стволовые опухолевые клетки»), «theranostics» («тераностика»), «nanomaterials» («наноматериалы»), «nanotheranostics» («нанотераностика»). После исключения статей, посвященных техническим аспектам молекулярно-биологических исследований, были проанализированы 57 публикаций, связанных с тераностикой трижды негативного рака молочной железы.</p></sec><sec><title>РЕЗУЛЬТАТЫ</title><p>РЕЗУЛЬТАТЫ: Мишени для тераностики трижды негативного рака ассоциированы с опухолевыми клетками и компонентами микроокружения. В статье представлены данные о составе и взаимодействии различных клеточных субпопуляций в микроокружении опухоли, а также о роли стволовых опухолевых клеток в его формировании. Приведены современные классификации трижды негативного рака молочной железы и данные о молекулярных дефектах, связанных с различными подтипами. Описаны мишени для тераностики, ассоциированные со стволовыми, дифференцированными опухолевыми клетками и компонентами микроокружения опухоли. Приведены собственные данные о характере распределения различных субпопуляций микроокружения, которые должны учитываться при выборе характера воздействия на опухоль. Проанализированы возможности и области применения разработанных к настоящему времени радиофармпрепаратов и препаратов на основе наночастиц.</p></sec><sec><title>ЗАКЛЮЧЕНИЕ</title><p>ЗАКЛЮЧЕНИЕ: Трижды негативный рак молочной железы характеризуется наличием большого числа биомаркеров, которые могут быть мишенями для диагностических и терапевтических препаратов. Для их селекции целесообразно использовать технологии искусственного интеллекта. Использование наночастиц позволяет снизить токсичность и обеспечить реализацию одновременно нескольких методов лечения.</p></sec></abstract><trans-abstract xml:lang="en"><sec><title>INTRODUCTION</title><p>INTRODUCTION: Triple negative cancer is one of the most aggressive subtypes of breast cancer. Currently, no effective treatment methods have been proposed that would significantly affect the long-term results of treatment.</p></sec><sec><title>OBJECTIVE</title><p>OBJECTIVE: To summarize the possibilities of theranostics and nanteranostics in the visualization and elimination of malignant cells and immunosuppressive cells of the microenvironment of thriple negative breast cancer.</p></sec><sec><title>MATERIALS AND METHODS</title><p>MATERIALS AND METHODS: A search was conducted for scientific publications in the PubMed information and analytical system for 2015–2022 by keywords: «triple negative breast cancer» («triple negative breast cancer»), «signaling pathways» («signaling pathways»), «tumor microenvironment» («tumor microenvironment»), «cancer stem cells» («stem tumor cells»), «theranostics», «nanomaterials» («nanomaterials»), «nanotheranostics» («nanoteranostics»). After excluding articles devoted to the technical aspects of molecular biological research, 57 publications related to the theranostics of thrice-negative breast cancer were analyzed.</p></sec><sec><title>RESULTS</title><p>RESULTS: Targets for theranostics of triple negative breast cancer are associated with tumor cells and components of the microenvironment. The article presents data on the composition and interaction between various cellular subpopulations in the tumor microenvironment, as well as on the role of cancer stem cells in its formation. State of art classifications of triple negative breast cancer and data on molecular defects associated with various subtypes are presented. Targets for theranostics associated with stem, differentiated tumor cells and components of the tumor microenvironment are described. The authors present their own data on the nature of the distribution of various subpopulations of the microenvironment, which should be taken into account when choosing the nature of the effect on the tumor. The possibilities and applications of radiopharmaceuticals and nanoparticle-based preparations developed to date have been analyzed.</p></sec><sec><title>CONCLUSION</title><p>CONCLUSION: Triple negative breast cancer is characterized by the presence of a large number of biomarkers that can be targets for diagnostic and therapeutic drugs. It is advisable to use artificial intelligence technologies for their selection. The use of nanoparticles makes it possible to reduce toxicity and ensure the implementation of several treatment methods simultaneously.</p></sec></trans-abstract><kwd-group xml:lang="ru"><kwd>трижды негативный рак молочной железы</kwd><kwd>сигнальные пути</kwd><kwd>микроокружение опухоли</kwd><kwd>стволовые опухолевые клетки</kwd><kwd>тераностика</kwd><kwd>наноматериалы</kwd><kwd>нанотераностика</kwd></kwd-group><kwd-group xml:lang="en"><kwd>triple negative breast cancer</kwd><kwd>signaling pathways</kwd><kwd>tumor microenvironment</kwd><kwd>cancer stem cells</kwd><kwd>theranostics</kwd><kwd>nanomaterials</kwd><kwd>nanotheranostics</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">Работа выполнена при финансовой поддержке Министерства здравоохранения Российской Федерации. Государственное задание 37.15–2021; 121040200135–3.</funding-statement><funding-statement xml:lang="en">The research was supported financially by Ministry of Health of the Russian Federation. State assignment 37.15–2021; 121040200135–3.</funding-statement></funding-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Hwang S.Y., Park S., Kwon Y. Recent therapeutic trends and promising targets in triple negative breast cancer // Pharmacology &amp; Therapeutics. 2019. Vol. 199. Р. 30–57. doi: 10.1016/j.pharmthera.2019.02.006.</mixed-citation><mixed-citation xml:lang="en">Hwang S.Y., Park S., Kwon Y. Recent therapeutic trends and promising targets in triple negative breast cancer // Pharmacology &amp; Therapeutics. 2019. Vol. 199. Р. 30–57. doi: 10.1016/j.pharmthera.2019.02.006.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Sung H., Ferlay J., Siegel R.L. et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries // CA: A Cancer Journal for Clinicians. 2021. Vol. 71, No. 3. Р. 209–249. doi: 10.3322/caac.21660.</mixed-citation><mixed-citation xml:lang="en">Sung H., Ferlay J., Siegel R.L. et al. Global cancer statistics 2020: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries // CA: A Cancer Journal for Clinicians. 2021. Vol. 71, No. 3. Р. 209–249. doi: 10.3322/caac.21660.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Состояние онкологической помощи населению России в 2019 году / под ред. А.Д.Каприна, В.В.Старинского, А.О.Шахзадовой. Москва: МНИОИ им. П.А.Герцена — филиал ФГБУ «НМИЦ радиологии» Минздрава России, 2020. 239 с.</mixed-citation><mixed-citation xml:lang="en">Kaprin A.D., Starinski V.V., Shachzadova A.O., editors. The state of oncological care to the population of Russian Federation in 2019. Moscow: MNIOI named after P.A.Gercen. 2020. 239 р. (In Russ.)].</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Perou C.M., Sorlie T., Eisen M.B. et al. Molecular portraits of human breast tumors // Nature. 2000. Vol. 406, No. 6797. Р. 747–752. doi: 10.1038/35021093.</mixed-citation><mixed-citation xml:lang="en">Perou C.M., Sorlie T., Eisen M.B. et al. Molecular portraits of human breast tumors // Nature. 2000. Vol. 406, No. 6797. Р. 747–752. doi: 10.1038/35021093.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Prat A., Perou C.M. Deconstruction the molecular portraits of breast cancer // Molecular Oncology. 2010. Vol. 5, No. 1. Р. 5–23. doi: 10.1016/j.molonc.2010.11.003.</mixed-citation><mixed-citation xml:lang="en">Prat A., Perou C.M. Deconstruction the molecular portraits of breast cancer // Molecular Oncology. 2010. Vol. 5, No. 1. Р. 5–23. doi: 10.1016/j.molonc.2010.11.003.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Perou C.M. Molecular stratification of triple-negative breast cancer // The Oncologist. 2011. Vol. 16 (suppl 1). Р. 61–70. doi: 10.1634/theoncologist.2011-S1-61.</mixed-citation><mixed-citation xml:lang="en">Perou C.M. Molecular stratification of triple-negative breast cancer // The Oncologist. 2011. Vol. 16 (suppl 1). Р. 61–70. doi: 10.1634/theoncologist.2011-S1-61.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Yao H., He G., Yan S. et al. Triple-negative breast cancer: is there a treatment on the horizon? // Oncotarget. 2016. Vol. 8, No. 1. Р. 1913–1924. doi: 10.18632/oncotarget.12284.</mixed-citation><mixed-citation xml:lang="en">Yao H., He G., Yan S. et al. Triple-negative breast cancer: is there a treatment on the horizon? // Oncotarget. 2016. Vol. 8, No. 1. Р. 1913–1924. doi: 10.18632/oncotarget.12284.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Fragomeni S.M., Sciallis A., Jeruss J.S. Molecular subtypes and local-regional control of breast cancer // Surgical Oncology Clinics of North America. 2018. Vol. 27, No. 1. Р. 95–120. doi: 10.1016/j.soc.2017.08.005.</mixed-citation><mixed-citation xml:lang="en">Fragomeni S.M., Sciallis A., Jeruss J.S. Molecular subtypes and local-regional control of breast cancer // Surgical Oncology Clinics of North America. 2018. Vol. 27, No. 1. Р. 95–120. doi: 10.1016/j.soc.2017.08.005.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Sharma P. Biology and management of patients with triple-negative breast cancer // The Oncologist. 2016. Vol. 21, No. 9. Р. 1050–1062. doi: 10.1634/theoncologist.2016–0067.</mixed-citation><mixed-citation xml:lang="en">Sharma P. Biology and management of patients with triple-negative breast cancer // The Oncologist. 2016. Vol. 21, No. 9. Р. 1050–1062. doi: 10.1634/theoncologist.2016–0067.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Bhushan A., Gonsalves A., Menon J.U. Current state of breast cancer diagnosis, treatment, and theranostics // Pharmaceutics. 2021. Vol. 13, No. 5. Р. 723. doi: 10.3390/pharmaceutics13050723.</mixed-citation><mixed-citation xml:lang="en">Bhushan A., Gonsalves A., Menon J.U. Current state of breast cancer diagnosis, treatment, and theranostics // Pharmaceutics. 2021. Vol. 13, No. 5. Р. 723. doi: 10.3390/pharmaceutics13050723.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Thakur V., Kutty R.V. Recent advances nanotheranostics for triple negative breast cancer treatment // Journal of Experimental &amp; Clinical Cancer Research. 2019. Vol. 38, No. 1. Р. 430. doi: 10.1186/s13046-019-1443-1.</mixed-citation><mixed-citation xml:lang="en">Thakur V., Kutty R.V. Recent advances nanotheranostics for triple negative breast cancer treatment // Journal of Experimental &amp; Clinical Cancer Research. 2019. Vol. 38, No. 1. Р. 430. doi: 10.1186/s13046-019-1443-1.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Curtis C., Shah S.P., Chin S.F. et al. The genomic and transcriptomic architecture of 2,000 breast tumors reveals novel subgroups // Nature. 2012. Vol. 486, No. 7403. Р. 346–352. doi: 10.1038/nature10983.</mixed-citation><mixed-citation xml:lang="en">Curtis C., Shah S.P., Chin S.F. et al. The genomic and transcriptomic architecture of 2,000 breast tumors reveals novel subgroups // Nature. 2012. Vol. 486, No. 7403. Р. 346–352. doi: 10.1038/nature10983.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Lehmann B.D., Pietenpol J.A. Identification and use of biomarkers in treatment strategies for triple-negative breast cancer subtypes // The Journal of Pathology. 2013. Vol. 232, No. 2. Р. 142–150. doi: 10.1002/path.4280.</mixed-citation><mixed-citation xml:lang="en">Lehmann B.D., Pietenpol J.A. Identification and use of biomarkers in treatment strategies for triple-negative breast cancer subtypes // The Journal of Pathology. 2013. Vol. 232, No. 2. Р. 142–150. doi: 10.1002/path.4280.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Burstein M.D., Tsimelzon A., Poage G.M. et al. Comprehensive genomic analysis identifies novel subtypes and targets of triple-negative breast cancer // Clinical Cancer Research. 2015. Vol. 21, No. 7. Р. 1688–1698. doi: 10.1158/1078-0432.CCR-14-0432.</mixed-citation><mixed-citation xml:lang="en">Burstein M.D., Tsimelzon A., Poage G.M. et al. Comprehensive genomic analysis identifies novel subtypes and targets of triple-negative breast cancer // Clinical Cancer Research. 2015. Vol. 21, No. 7. Р. 1688–1698. doi: 10.1158/1078-0432.CCR-14-0432.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Liu Y.R., Jiang Y.Z., Xu X.E. et al. Comprehensive transcriptome analysis identifies novel molecular subtypes and subtype-specific RNAs of triple-negative breast cancer // Breast Cancer Res. 2016. Vol. 18, No. 1. doi: 10.1186/s13058-016-0690-8.</mixed-citation><mixed-citation xml:lang="en">Liu Y.R., Jiang Y.Z., Xu X.E. et al. Comprehensive transcriptome analysis identifies novel molecular subtypes and subtype-specific RNAs of triple-negative breast cancer // Breast Cancer Res. 2016. Vol. 18, No. 1. doi: 10.1186/s13058-016-0690-8.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Walcher L., Kistenmacher A.K., Suo H. et al. Cancer stem cells — origins and biomarkers: perspectives for targeted personalized therapies // Frontiers in Immunology. 2020. Vol. 11. doi: 10.3389/fimmu.2020.01280.</mixed-citation><mixed-citation xml:lang="en">Walcher L., Kistenmacher A.K., Suo H. et al. Cancer stem cells — origins and biomarkers: perspectives for targeted personalized therapies // Frontiers in Immunology. 2020. Vol. 11. doi: 10.3389/fimmu.2020.01280.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Sivaganesh V., Promi N., Maher S., Peethambaran B. Emerging immunotherapies against novel molecular targets in breast cancer // International Journal of Molecular Sciences. 2021. Vol. 22, No. 5. Р. 2433. doi: 10.3390/ijms22052433.</mixed-citation><mixed-citation xml:lang="en">Sivaganesh V., Promi N., Maher S., Peethambaran B. Emerging immunotherapies against novel molecular targets in breast cancer // International Journal of Molecular Sciences. 2021. Vol. 22, No. 5. Р. 2433. doi: 10.3390/ijms22052433.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Pawar A., Prabhu P. Nanosodliers: a promising strategy to combat triple negative breast cancer // Biomedicine &amp; Pharmacotherapy. 2019. Vol. 110. Р. 319–341. doi: 10.1016/j.biopha.2018.11.122.</mixed-citation><mixed-citation xml:lang="en">Pawar A., Prabhu P. Nanosodliers: a promising strategy to combat triple negative breast cancer // Biomedicine &amp; Pharmacotherapy. 2019. Vol. 110. Р. 319–341. doi: 10.1016/j.biopha.2018.11.122.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Fang H., Cavaliere A., Li Z. et al. Preclinical advances in theranostics for the different molecular subtypes of breast cancer // Frontiers in Pharmacology. 2021. Vol. 9, No. 12. P. 627693. doi: 10.3389/fphar.2021.627693.</mixed-citation><mixed-citation xml:lang="en">Fang H., Cavaliere A., Li Z. et al. Preclinical advances in theranostics for the different molecular subtypes of breast cancer // Frontiers in Pharmacology. 2021. Vol. 9, No. 12. P. 627693. doi: 10.3389/fphar.2021.627693.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Molchanov O.E., Maistrenko D.N., Granov D.A. et al. Biomarkers and potential targets for immune and cellular therapy in triple negative breast cancer // Cellular Therapy and Transplantation. 2022. Vol. 11, No. 2. Р. 16–30. doi: 10.18620/ctt-1866-8836-2022-11-2-16-30.</mixed-citation><mixed-citation xml:lang="en">Molchanov O.E., Maistrenko D.N., Granov D.A. et al. Biomarkers and potential targets for immune and cellular therapy in triple negative breast cancer // Cellular Therapy and Transplantation. 2022. Vol. 11, No. 2. Р. 16–30. doi: 10.18620/ctt-1866-8836-2022-11-2-16-30.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Schaefer N., Prior J.O., Schottelius M. From theranostics to immunotheranostics: the concept // Nuclear Medicine and Molecular Imaging. 2020. Vol. 54, No. 2. Р. 81–85. doi: 10.1007/s13139-020-00639-6.</mixed-citation><mixed-citation xml:lang="en">Schaefer N., Prior J.O., Schottelius M. From theranostics to immunotheranostics: the concept // Nuclear Medicine and Molecular Imaging. 2020. Vol. 54, No. 2. Р. 81–85. doi: 10.1007/s13139-020-00639-6.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Sgouros G., Bodei L., McDevit M.R., Nedrow J.R. Radiopharmaceutical therapy in cancer: clinical advances and challenges // Nature Reviews Drug Discovery. 2020. Vol. 19, No. 9. Р. 589–608. doi: 10.1038/s41573-020-0073-9.</mixed-citation><mixed-citation xml:lang="en">Sgouros G., Bodei L., McDevit M.R., Nedrow J.R. Radiopharmaceutical therapy in cancer: clinical advances and challenges // Nature Reviews Drug Discovery. 2020. Vol. 19, No. 9. Р. 589–608. doi: 10.1038/s41573-020-0073-9.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Freise A.S., Wu A.M. In vivo imaging with antibodies and engineered fragments // Molecular Immunology. 2015. Vol. 67, No. 2. Р. 142–152. doi: 10.1016/j.molimm.2015.04.001.</mixed-citation><mixed-citation xml:lang="en">Freise A.S., Wu A.M. In vivo imaging with antibodies and engineered fragments // Molecular Immunology. 2015. Vol. 67, No. 2. Р. 142–152. doi: 10.1016/j.molimm.2015.04.001.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Gosmann D., Russelli L., Weber W.A. et al. Promise and challenges of clinical non-invasive T-cell tracking in the era of cancer immunotherapy // EJNMMI Research. 2022. Vol. 12, No. 5. doi: 10.1186/s13550-022-00877-z.</mixed-citation><mixed-citation xml:lang="en">Gosmann D., Russelli L., Weber W.A. et al. Promise and challenges of clinical non-invasive T-cell tracking in the era of cancer immunotherapy // EJNMMI Research. 2022. Vol. 12, No. 5. doi: 10.1186/s13550-022-00877-z.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang C., Yu X., Gao L. et al. Noninvasive imaging of CD206-positive M2 macrophages as an early biomarker for post-chemotherapy tumor relapse and lymph node metastasis // Theranostics. 2017. Vol. 7, No. 17. Р. 4276–4288. doi: 10.7150/thno.20999.</mixed-citation><mixed-citation xml:lang="en">Zhang C., Yu X., Gao L. et al. Noninvasive imaging of CD206-positive M2 macrophages as an early biomarker for post-chemotherapy tumor relapse and lymph node metastasis // Theranostics. 2017. Vol. 7, No. 17. Р. 4276–4288. doi: 10.7150/thno.20999.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Giesel F.L., Kratochwil C., Lindner T. et al. 68Ga-FAPI PET/CT: biodistribution and preliminary dosimetry estimate of 2 DOTA-containing FAP-targeting agents in patients with various cancers // Journal of Nuclear Medicine. 2018. Vol. 60, No. 3. Р. 386–392. doi: 10.2967/jnumed.118.215913.</mixed-citation><mixed-citation xml:lang="en">Giesel F.L., Kratochwil C., Lindner T. et al. 68Ga-FAPI PET/CT: biodistribution and preliminary dosimetry estimate of 2 DOTA-containing FAP-targeting agents in patients with various cancers // Journal of Nuclear Medicine. 2018. Vol. 60, No. 3. Р. 386–392. doi: 10.2967/jnumed.118.215913.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Wolska-Washer A., Robak T. Safety and tolerability of antibody-drug conjugates in cancer // Drug Safety. 2019. Vol. 42, No. 2. Р. 295–314. doi: 10.1007/s40264018-0775-7.</mixed-citation><mixed-citation xml:lang="en">Wolska-Washer A., Robak T. Safety and tolerability of antibody-drug conjugates in cancer // Drug Safety. 2019. Vol. 42, No. 2. Р. 295–314. doi: 10.1007/s40264018-0775-7.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Bardia A., Mayer I.A., Vahdat L.T. et al. Sacituzumab Govitecan-hziy in refractory metastatic triple-negative breast cancer // New England Journal of Medicine. 2019. Vol. 380, No. 8. Р. 741–751. doi: 10.1056/nejmc1903943.</mixed-citation><mixed-citation xml:lang="en">Bardia A., Mayer I.A., Vahdat L.T. et al. Sacituzumab Govitecan-hziy in refractory metastatic triple-negative breast cancer // New England Journal of Medicine. 2019. Vol. 380, No. 8. Р. 741–751. doi: 10.1056/nejmc1903943.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Nejadmoghaddam M.R., Minai-Tehrani A., Ghahremanzadeh R. et al. Antibody-drug conjugates: possibilities and challenges // Avicenna journal of medical biotechnology. 2019. Vol. 11, No. 1. Р. 3–23.</mixed-citation><mixed-citation xml:lang="en">Nejadmoghaddam M.R., Minai-Tehrani A., Ghahremanzadeh R. et al. Antibody-drug conjugates: possibilities and challenges // Avicenna journal of medical biotechnology. 2019. Vol. 11, No. 1. Р. 3–23.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Gomez-Roca C.A., Boni V., Moreno V. et al. A phase I study of SAR566658, an anti- CA6-antibody drug conjugate (ADC) in patients with CA6-positive advanced solid tumors (NCT01156870) // Journal of Clinical Oncology. 2016. Vol. 34 (Suppl. 15). Р. 2511. doi: 10.1200/jco.2016.34.15_suppl.2511.</mixed-citation><mixed-citation xml:lang="en">Gomez-Roca C.A., Boni V., Moreno V. et al. A phase I study of SAR566658, an anti- CA6-antibody drug conjugate (ADC) in patients with CA6-positive advanced solid tumors (NCT01156870) // Journal of Clinical Oncology. 2016. Vol. 34 (Suppl. 15). Р. 2511. doi: 10.1200/jco.2016.34.15_suppl.2511.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Li W., Yang H., Li X. et al. Signaling pathway inhibitors target breast cancer stem cells in triple-negative breast cancer // Oncology Reports. 2018. Vol. 41, No. 1. P. 437–446. doi: 10.3892/or.2018.6805.</mixed-citation><mixed-citation xml:lang="en">Li W., Yang H., Li X. et al. Signaling pathway inhibitors target breast cancer stem cells in triple-negative breast cancer // Oncology Reports. 2018. Vol. 41, No. 1. P. 437–446. doi: 10.3892/or.2018.6805.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Hung C.H., Chen F.M., Lin Y.C. et al. Altered monocyte differentiation and macrophage polarization patterns in patients with breast cancer // BMC Cancer. 2018. Vol. 18, No. 1. doi: 10.1186/s12885-018-4284-y.</mixed-citation><mixed-citation xml:lang="en">Hung C.H., Chen F.M., Lin Y.C. et al. Altered monocyte differentiation and macrophage polarization patterns in patients with breast cancer // BMC Cancer. 2018. Vol. 18, No. 1. doi: 10.1186/s12885-018-4284-y.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Millrud C.R., Bergenfelz C., Leandersson K. On the origin of myeloid-derived suppressor cells // Oncotarget. 2016. Vol. 8, No. 2. Р. 3649–3665. doi: 10.18632/oncotarget.12278.</mixed-citation><mixed-citation xml:lang="en">Millrud C.R., Bergenfelz C., Leandersson K. On the origin of myeloid-derived suppressor cells // Oncotarget. 2016. Vol. 8, No. 2. Р. 3649–3665. doi: 10.18632/oncotarget.12278.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Wculek S.K., Cueto F.J., Mujal A.M. et al. Dendritic cells in cancer immunology and immunotherapy // Nature Reviews Immunology. 2019. Vol. 20, No. 1. Р. 7– 24. doi: 10.1038/s41577-019-0210-z.</mixed-citation><mixed-citation xml:lang="en">Wculek S.K., Cueto F.J., Mujal A.M. et al. Dendritic cells in cancer immunology and immunotherapy // Nature Reviews Immunology. 2019. Vol. 20, No. 1. Р. 7– 24. doi: 10.1038/s41577-019-0210-z.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Lorenzo-Sanz L., Muñoz P. Tumor-infiltrating immunosuppressive cells in cancer-cell plasticity, tumor progression and therapy response // Cancer Microenvironment. 2019. Vol. 12, No. 2–3. Р. 119–132. doi: 10.1007/s12307-019-00232-2.</mixed-citation><mixed-citation xml:lang="en">Lorenzo-Sanz L., Muñoz P. Tumor-infiltrating immunosuppressive cells in cancer-cell plasticity, tumor progression and therapy response // Cancer Microenvironment. 2019. Vol. 12, No. 2–3. Р. 119–132. doi: 10.1007/s12307-019-00232-2.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Chiossone L., Dumas P.Y., Vienne M., Vivier E. Natural killer cells and other innate lymphoid cells in cancer // Nature Reviews Immunology. 2018. Vol. 18, No. 11. Р. 671–688. doi: 10.1038/s41577-018-0061-z.</mixed-citation><mixed-citation xml:lang="en">Chiossone L., Dumas P.Y., Vienne M., Vivier E. Natural killer cells and other innate lymphoid cells in cancer // Nature Reviews Immunology. 2018. Vol. 18, No. 11. Р. 671–688. doi: 10.1038/s41577-018-0061-z.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Lin L., Hu X., Zhang H., Hu H. Tertiary lymphoid organs in cancer immunology: mechanisms and the new strategies for immunotherapy // Frontiers in Immunology. 2019. Vol. 10. doi: 10.3389/fimmu.2019.01398.</mixed-citation><mixed-citation xml:lang="en">Lin L., Hu X., Zhang H., Hu H. Tertiary lymphoid organs in cancer immunology: mechanisms and the new strategies for immunotherapy // Frontiers in Immunology. 2019. Vol. 10. doi: 10.3389/fimmu.2019.01398.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Galon J., Bruni D. Approaches to treat immune hot, altered and cold tumors with combination immunotherapies // Nature Reviews Drug Discovery. 2019. Vol. 18, No. 3. Р. 197–218. doi: 10.1038/s41573-018-0007-y.</mixed-citation><mixed-citation xml:lang="en">Galon J., Bruni D. Approaches to treat immune hot, altered and cold tumors with combination immunotherapies // Nature Reviews Drug Discovery. 2019. Vol. 18, No. 3. Р. 197–218. doi: 10.1038/s41573-018-0007-y.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Chan C., Fonge H., Lam K., Reilly R.M. Effectiveness and normal tissue toxicity of auger electron (AE) radioimmunotherapy (RIT) with [111In]In-Bn-DTPA-nimotuzumab in mice with triple-negative or trastuzumab-resistant human breast cancer xenografts that overexpress EGFR // Nuclear Medicine and Biology. 2019. Vol. 80–81. Р. 37–44. doi: 10.1016/j.nucmedbio.2019.10.001.</mixed-citation><mixed-citation xml:lang="en">Chan C., Fonge H., Lam K., Reilly R.M. Effectiveness and normal tissue toxicity of auger electron (AE) radioimmunotherapy (RIT) with [111In]In-Bn-DTPA-nimotuzumab in mice with triple-negative or trastuzumab-resistant human breast cancer xenografts that overexpress EGFR // Nuclear Medicine and Biology. 2019. Vol. 80–81. Р. 37–44. doi: 10.1016/j.nucmedbio.2019.10.001.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Erdmann S., Niederstadt L., Koziolek E.J. et al. CMKLR1-targeting peptide tracers for PET/MR imaging of breast cancer // Theranostics. 2019. Vol. 9, No. 22. Р. 6719–6733. doi: 10.7150/thno.34857.</mixed-citation><mixed-citation xml:lang="en">Erdmann S., Niederstadt L., Koziolek E.J. et al. CMKLR1-targeting peptide tracers for PET/MR imaging of breast cancer // Theranostics. 2019. Vol. 9, No. 22. Р. 6719–6733. doi: 10.7150/thno.34857.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Meng Q., Li F., Jiang S., Li Z. Novel 64Cu-labeled CUDC-101 for in Vivo PET imaging of histone deacetylases // ACS Medicinal Chemistry Letters. 2013. Vol. 4, No. 9. Р. 858–862. doi: 10.1021/ml400191z.</mixed-citation><mixed-citation xml:lang="en">Meng Q., Li F., Jiang S., Li Z. Novel 64Cu-labeled CUDC-101 for in Vivo PET imaging of histone deacetylases // ACS Medicinal Chemistry Letters. 2013. Vol. 4, No. 9. Р. 858–862. doi: 10.1021/ml400191z.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Henry K.E., Dilling T.R., Abdel-Atti D. et al. Noninvasive 89Zr-transferrin PET shows improved tumor targeting compared with 18F-FDG PET in MYC-overexpressing human triple-negative breast cancer // Journal of Nuclear Medicine. 2017. Vol. 59, No. 1. Р. 51–57. doi: 10.2967/jnumed.117.192286.</mixed-citation><mixed-citation xml:lang="en">Henry K.E., Dilling T.R., Abdel-Atti D. et al. Noninvasive 89Zr-transferrin PET shows improved tumor targeting compared with 18F-FDG PET in MYC-overexpressing human triple-negative breast cancer // Journal of Nuclear Medicine. 2017. Vol. 59, No. 1. Р. 51–57. doi: 10.2967/jnumed.117.192286.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Shi S., Hong H., Orbay H. et al. ImmunoPET of tissue factor expression in triple-negative breast cancer with a radiolabeled antibody Fab fragment // European Journal of Nuclear Medicine and Molecular Imaging. 2015. Vol. 42, No. 8. Р. 1295–1303. doi: 10.1007/s00259-015-3038-1.</mixed-citation><mixed-citation xml:lang="en">Shi S., Hong H., Orbay H. et al. ImmunoPET of tissue factor expression in triple-negative breast cancer with a radiolabeled antibody Fab fragment // European Journal of Nuclear Medicine and Molecular Imaging. 2015. Vol. 42, No. 8. Р. 1295–1303. doi: 10.1007/s00259-015-3038-1.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Pascual L., Cerqueira-Coutinho C., García-Fernández A. et al. MUC1 aptamer-capped mesoporous silica nanoparticles for controlled drug delivery and radio-imaging applications // Nanomedicine: Nanotechnology, Biology and Medicine. 2017. Vol. 13, No. 8. Р. 2495–2505. doi: 10.1016/j.nano.2017.08.006.</mixed-citation><mixed-citation xml:lang="en">Pascual L., Cerqueira-Coutinho C., García-Fernández A. et al. MUC1 aptamer-capped mesoporous silica nanoparticles for controlled drug delivery and radio-imaging applications // Nanomedicine: Nanotechnology, Biology and Medicine. 2017. Vol. 13, No. 8. Р. 2495–2505. doi: 10.1016/j.nano.2017.08.006.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Fu P., Shen B., Zhao C., Tian G. Molecular imaging of MDM2 messenger RNA with 99mTc-labeled antisense oligonucleotides in experimental human breast cancer xenografts // Journal of Nuclear Medicine. 2010. Vol. 51, No. 11. Р. 1805–1812. doi: 10.2967/jnumed.110.077982.</mixed-citation><mixed-citation xml:lang="en">Fu P., Shen B., Zhao C., Tian G. Molecular imaging of MDM2 messenger RNA with 99mTc-labeled antisense oligonucleotides in experimental human breast cancer xenografts // Journal of Nuclear Medicine. 2010. Vol. 51, No. 11. Р. 1805–1812. doi: 10.2967/jnumed.110.077982.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Aranda-Lara L., Ferro-Flores G., Azorín-Vega E. et al. Synthesis and evaluation of Lys 1 (a,g-Folate)Lys 3 (177Lu-DOTA)-Bombesin(1–14) as a potential theranostic radiopharmaceutical for breast cancer // Applied Radiation and Isotopes. 2016. Vol. 107. Р. 214–219. doi: 10.1016/j.apradiso.2015.10.030.</mixed-citation><mixed-citation xml:lang="en">Aranda-Lara L., Ferro-Flores G., Azorín-Vega E. et al. Synthesis and evaluation of Lys 1 (a,g-Folate)Lys 3 (177Lu-DOTA)-Bombesin(1–14) as a potential theranostic radiopharmaceutical for breast cancer // Applied Radiation and Isotopes. 2016. Vol. 107. Р. 214–219. doi: 10.1016/j.apradiso.2015.10.030.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Cavaliere A., Sun S., Lee S. et al. Development of [89Zr]ZrDFO-amivantamab bispecific to EGFR and c-MET for PET imaging of triple-negative breast cancer // European Journal of Nuclear Medicine and Molecular Imaging. 2020. Vol. 48, No. 2. Р. 383–394. doi: 10.1007/s00259-020-04978-6.</mixed-citation><mixed-citation xml:lang="en">Cavaliere A., Sun S., Lee S. et al. Development of [89Zr]ZrDFO-amivantamab bispecific to EGFR and c-MET for PET imaging of triple-negative breast cancer // European Journal of Nuclear Medicine and Molecular Imaging. 2020. Vol. 48, No. 2. Р. 383–394. doi: 10.1007/s00259-020-04978-6.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Waaijer S.J.H., Warnders F.J., Stienen S. et al. Molecular imaging of radiolabeled bispecific T-cell engager 89Zr-AMG211 targeting CEA-positive tumors // Clinical Cancer Research. 2018. Vol. 24, No. 20. Р. 4988–4996. doi: 10.1158/1078-0432.Ccr-18-0786.</mixed-citation><mixed-citation xml:lang="en">Waaijer S.J.H., Warnders F.J., Stienen S. et al. Molecular imaging of radiolabeled bispecific T-cell engager 89Zr-AMG211 targeting CEA-positive tumors // Clinical Cancer Research. 2018. Vol. 24, No. 20. Р. 4988–4996. doi: 10.1158/1078-0432.Ccr-18-0786.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Gai Y., Jiang Y., Long Y. et al. Evaluation of an integrin avb3 and aminopeptidase N dual-receptor targeting tracer for breast cancer imaging // Molecular Pharmaceutics. 2020. Vol. 17, No. 1. Р. 349–358. doi: 10.1021/acs.molpharmaceut.9b01134.</mixed-citation><mixed-citation xml:lang="en">Gai Y., Jiang Y., Long Y. et al. Evaluation of an integrin avb3 and aminopeptidase N dual-receptor targeting tracer for breast cancer imaging // Molecular Pharmaceutics. 2020. Vol. 17, No. 1. Р. 349–358. doi: 10.1021/acs.molpharmaceut.9b01134.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Morgenroth A., Tinkir E., Vogg A. T. et al. Targeting of prostate-specific membrane antigen for radio-ligand therapy of triple-negative breast cancer // Breast Cancer Research. 2019. Vol. 21, No. 1. doi: 10.1186/s13058-019-1205-1.</mixed-citation><mixed-citation xml:lang="en">Morgenroth A., Tinkir E., Vogg A. T. et al. Targeting of prostate-specific membrane antigen for radio-ligand therapy of triple-negative breast cancer // Breast Cancer Research. 2019. Vol. 21, No. 1. doi: 10.1186/s13058-019-1205-1.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Dai W., Yang F., Ma L. et al. Combined mTOR inhibitor rapamycin and doxorubicin-loaded cyclic octapeptide modified liposomes for targeting integrin a3 in triplenegative breast cancer // Biomaterials. 2014. Vol. 35, No. 20. Р. 5347–5358. doi: 10.1016/j.biomaterials.2014.03.036.</mixed-citation><mixed-citation xml:lang="en">Dai W., Yang F., Ma L. et al. Combined mTOR inhibitor rapamycin and doxorubicin-loaded cyclic octapeptide modified liposomes for targeting integrin a3 in triplenegative breast cancer // Biomaterials. 2014. Vol. 35, No. 20. Р. 5347–5358. doi: 10.1016/j.biomaterials.2014.03.036.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Kutty R.V., Feng S-S. Cetuximab conjugated vitamin E TPGS micelles for targeted delivery of docetaxel for treatment of triple negative breast cancers // Biomaterials. 2013. Vol. 34, No. 38. Р. 10160–10171. doi: 10.1016/j.biomaterials.2013.09.043.</mixed-citation><mixed-citation xml:lang="en">Kutty R.V., Feng S-S. Cetuximab conjugated vitamin E TPGS micelles for targeted delivery of docetaxel for treatment of triple negative breast cancers // Biomaterials. 2013. Vol. 34, No. 38. Р. 10160–10171. doi: 10.1016/j.biomaterials.2013.09.043.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Finlay J., Roberts C.M., Lowe G. et al. RNA-based TWIST1 inhibition via dendrimer complex to reduce breast cancer cell metastasis // BioMed Research International. 2015. Vol. 2015. Р. 1–12. doi: 10.1155/2015/382745.</mixed-citation><mixed-citation xml:lang="en">Finlay J., Roberts C.M., Lowe G. et al. RNA-based TWIST1 inhibition via dendrimer complex to reduce breast cancer cell metastasis // BioMed Research International. 2015. Vol. 2015. Р. 1–12. doi: 10.1155/2015/382745.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang L., Varma N.R., Gang Z.Z. et al. Targeting triple negative breast cancer with a small-sized paramagnetic nanoparticle // Journal of Nanomedicine &amp; Nanotechnology. 2016. Vol. 7, No. 5. doi: 10.4172/2157-7439.1000404.</mixed-citation><mixed-citation xml:lang="en">Zhang L., Varma N.R., Gang Z.Z. et al. Targeting triple negative breast cancer with a small-sized paramagnetic nanoparticle // Journal of Nanomedicine &amp; Nanotechnology. 2016. Vol. 7, No. 5. doi: 10.4172/2157-7439.1000404.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Andey T., Sudhakar G., Marepally S. et al. Lipid nanocarriers of a lipid-conjugated estrogenic derivative inhibit tumor growth and enhance cisplatin activity against triple-negative breast cancer: pharmacokinetic and efficacy evaluation // Molecular Pharmaceutics. 2015. Vol. 12, No. 4. Р. 1105–1120. doi: 10.1021/mp5008629.</mixed-citation><mixed-citation xml:lang="en">Andey T., Sudhakar G., Marepally S. et al. Lipid nanocarriers of a lipid-conjugated estrogenic derivative inhibit tumor growth and enhance cisplatin activity against triple-negative breast cancer: pharmacokinetic and efficacy evaluation // Molecular Pharmaceutics. 2015. Vol. 12, No. 4. Р. 1105–1120. doi: 10.1021/mp5008629.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Wu Y., Wang H., Gao F. et al. An injectable supramolecular polymer nanocomposite hydrogel for prevention of breast cancer recurrence with theranostic and mammoplastic functions // Advanced Functional Materials. 2018. Vol. 28, No. 12. P. 1801000. doi: 10.1002/adfm.201801000.</mixed-citation><mixed-citation xml:lang="en">Wu Y., Wang H., Gao F. et al. An injectable supramolecular polymer nanocomposite hydrogel for prevention of breast cancer recurrence with theranostic and mammoplastic functions // Advanced Functional Materials. 2018. Vol. 28, No. 12. P. 1801000. doi: 10.1002/adfm.201801000.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Bouaud J., Pelayo S., Lamy J.B. et al. Implementation of an ontological reasoning to support the guideline-based management of primary breast cancer patients in the desire project // Artificial Intelligence in Medicine. 2020. Vol. 108. Р. 101922. doi: 10.1016/j.artmed.2020.101922.</mixed-citation><mixed-citation xml:lang="en">Bouaud J., Pelayo S., Lamy J.B. et al. Implementation of an ontological reasoning to support the guideline-based management of primary breast cancer patients in the desire project // Artificial Intelligence in Medicine. 2020. Vol. 108. Р. 101922. doi: 10.1016/j.artmed.2020.101922.</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>
