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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">Acta Naturae</journal-id><journal-title-group><journal-title xml:lang="en">Acta Naturae</journal-title><trans-title-group xml:lang="ru"><trans-title>Acta Naturae</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-8251</issn><publisher><publisher-name xml:lang="en">Acta Naturae Ltd</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">11611</article-id><article-id pub-id-type="doi">10.32607/actanaturae.11611</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 Evolution of Targeted Radionuclide Diagnosis of HER2-Positive Breast Cancer</article-title><trans-title-group xml:lang="ru"><trans-title>Эволюция таргетной радионуклидной диагностики HER2-позитивного рака молочной железы</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Bragina</surname><given-names>Olga D.</given-names></name><name xml:lang="ru"><surname>Брагина</surname><given-names>Ольга Дмитриевна</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>rungis@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Deyev</surname><given-names>Sergei M.</given-names></name><name xml:lang="ru"><surname>Деев</surname><given-names>Сергей Михайлович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>rungis@mail.ru</email><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Chernov</surname><given-names>Vladimir I.</given-names></name><name xml:lang="ru"><surname>Чернов</surname><given-names>Владимир Иванович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>rungis@mail.ru</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Tolmachev</surname><given-names>Vladimir M.</given-names></name><name xml:lang="ru"><surname>Толмачев</surname><given-names>Владимир Максимиллианович</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><email>rungis@mail.ru</email><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff4"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Tomsk National Research Medical Center of the Russian Academy of Sciences Cancer Research institute</institution></aff><aff><institution xml:lang="ru">Томский национальный исследовательский медицинский центр РАН</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">National Research Tomsk Polytechnic University</institution></aff><aff><institution xml:lang="ru">Национальный исследовательский Томский политехнический университет</institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry of the Russian Academy of Sciences</institution></aff><aff><institution xml:lang="ru">Институт биоорганической химии им. академиков М.М. Шемякина и Ю.А. Овчинникова РАН</institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">Uppsala University</institution></aff><aff><institution xml:lang="ru">Упсальский университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2022-07-21" publication-format="electronic"><day>21</day><month>07</month><year>2022</year></pub-date><volume>14</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>4</fpage><lpage>15</lpage><history><date date-type="received" iso-8601-date="2021-10-20"><day>20</day><month>10</month><year>2021</year></date><date date-type="accepted" iso-8601-date="2022-03-16"><day>16</day><month>03</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2022, Bragina O.D., Deyev S.M., Chernov V.I., Tolmachev V.M.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2022, Брагина О.Д., Деев С.М., Чернов В.И., Толмачев В.М.</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="en">Bragina O.D., Deyev S.M., Chernov V.I., Tolmachev V.M.</copyright-holder><copyright-holder xml:lang="ru">Брагина О.Д., Деев С.М., Чернов В.И., Толмачев В.М.</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://actanaturae.ru/2075-8251/article/view/11611">https://actanaturae.ru/2075-8251/article/view/11611</self-uri><abstract xml:lang="en"><p>This review examines the evolution of the radionuclide diagnosis of HER2-positive breast cancer using various compounds as a targeting module in clinical practice: from full-length antibodies to a new group of small synthetic proteins called alternative scaffold proteins. This topic is of especial relevance today in view of the problems attendant to the detection of breast cancer with HER2/neu overexpression, which, in most cases, introduce errors in the treatment of patients. The results of clinical studies of radiopharmaceuticals based on affibody molecules, ADAPTs, and DARPins for SPECT and PET have demonstrated good tolerability of the compounds, their rapid excretion from the body, and the possibility to differentiate tumor sites depending on the HER2/neu status. This indicates that targeted radionuclide diagnosis holds promise and the need to continue research in this direction.</p></abstract><trans-abstract xml:lang="ru"><p>Представленный обзор посвящен «клинической» эволюции радионуклидной диагностики HER2-позитивного рака молочной железы с использованием в качестве «нацеливающего» модуля различных структур – от «полноразмерных» антител до новой группы синтетических белков небольшого размера – альтернативных каркасных белков. Эта тематика особенно актуальна в связи с существующими проблемами выявления злокачественных опухолей молочной железы с гиперэкспрессией HER2/neu, что во многих случаях ведет к назначению неадекватного системного лечения у пациентов этой категории. Результаты клинических исследований радиофармпрепаратов на основе молекул аффибоди, адаптов и дарпинов для ОФЭКТ и ПЭТ продемонстрировали их хорошую переносимость, быстрое выведение из организма и возможность дифференцировки опухолевых очагов в зависимости от статуса рецептора эпидермального фактора роста HER2/neu, что свидетельствует о перспективности таргетной радионуклидной диагностики и необходимости продолжения исследований в данном направлении.</p></trans-abstract><kwd-group xml:lang="en"><kwd>breast cancer</kwd><kwd>HER2/neu</kwd><kwd>radionuclide diagnostics</kwd><kwd>monoclonal antibody</kwd><kwd>alternative scaffold proteins</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>рак молочной железы</kwd><kwd>HER2/neu</kwd><kwd>радионуклидная диагностика</kwd><kwd>моноклональное антитело</kwd><kwd>альтернативные каркасные белки</kwd></kwd-group><funding-group><award-group><funding-source><institution-wrap><institution xml:lang="ru">Министерство науки и высшего образования Российской Федерации</institution></institution-wrap><institution-wrap><institution xml:lang="en">Ministry of Science and Higher Education of the Russian Federation</institution></institution-wrap></funding-source><award-id>075-15-2022-1103</award-id></award-group><funding-statement xml:lang="en">The work was carried out within the framework of the grant of the Ministry of Science and Higher Education Agreement No. 075-15-2019-1925 on the topic "Development of target molecules based on scaffold proteins for the diagnosis and therapy of malignant neoplasms: theranostic approach".</funding-statement><funding-statement xml:lang="ru">Работа выполнена в рамках гранта Министерства науки и высшего образования соглашение № 075-15-2019-1925 по теме "Разработка таргетных молекул на основе каркасных белков для диагностики и терапии злокачественных новообразований: тераностический подход".</funding-statement></funding-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Kaprin A.D., Starinskii V.V., Petrova G.V. 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