<?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">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.2024.002</article-id><article-id custom-type="elpub" pub-id-type="custom">mes-28</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>Молекулярно-генетическое тестирование в контексте медико-биологических рисков здоровью космонавтов</article-title><trans-title-group xml:lang="en"><trans-title>Molecular genetic studies in the context of biomedical risks for cosmonauts' health</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>Латарцев</surname><given-names>К. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Latartsev</surname><given-names>K. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Константин Владимирович Латарцев</p><p>ул. Щукинская, д. 5, стр. 4, г. Москва, 123182</p></bio><bio xml:lang="en"><p>Konstantin V. Latartsev</p><p>Shchukinskaya, 5, str. 2, Moscow, 123182</p></bio><email xlink:type="simple">k.latartsev@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Каспранский</surname><given-names>Р. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Kaspranskiy</surname><given-names>R. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Москва</p></bio><bio xml:lang="en"><p>Moscow</p></bio><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Федеральный научно-клинический центр космической медицины Федерального медико-биологического агентства; Московский государственный университет имени М. В. Ломоносова</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Federal State Budgetary Institution “Federal Research and Clinic Center of Space Medicine” of the Federal Biomedical Agency; Lomonosov Moscow State University</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>22</day><month>10</month><year>2024</year></pub-date><volume>26</volume><issue>1</issue><fpage>5</fpage><lpage>12</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Латарцев К.В., Каспранский Р.Р., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Латарцев К.В., Каспранский Р.Р.</copyright-holder><copyright-holder xml:lang="en">Latartsev K.V., Kaspranskiy R.R.</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/28">https://www.extrememedicine.ru/jour/article/view/28</self-uri><abstract><p>Генетические исследования сегодня позволяют получить достаточно большое количество информации о человеке, на основе которой иногда возможно прогнозировать риски возникновения определенных заболеваний. Это дает основания полагать, что подобное тестирование можно применять и в области пилотируемых космических полетов с целью выявления кандидатов, наиболее приспособленных к специфическим рискам. В статье рассмотрены публикации, посвященные генетическим полиморфизмам и их влиянию на фенотип носителя, а именно на проявления, представляющие интерес в контексте рисков, возникающих во время длительных космических полетов. Перечислены конкретные гены и приведены примеры аллельных вариантов. Уделено также внимание публикациям, описывающим новые молекулярные методы наблюдения за здоровьем человека, определены биомаркеры, которые могут быть использованы для исследований в интересах регулярного обследования действующих космонавтов.</p></abstract><trans-abstract xml:lang="en"><p>Today, genetic studies yield quite a large amount of information about a person, which, in many cases, allows predicting the risks of certain diseases. This gives grounds to believe that such testing can also be applied in the field of manned spaceflights in order to identify candidates best adapted to specific risks. The article examines publications on genetic polymorphisms and their effects on the carrier phenotype, namely, on such manifestations that are of interest in the context of risks arising during long-term space flights. Specific genes are listed and examples of allelic variants are given. Publications describing new molecular methods of monitoring human health are also considered, biomarkers that can be used for research in the interests of regular examination of active astronauts are identified.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>генетическая предрасположенность</kwd><kwd>молекулярные маркёры</kwd><kwd>риски длительных космических полетов</kwd><kwd>отбор космонавтов</kwd></kwd-group><kwd-group xml:lang="en"><kwd>genetic predisposition</kwd><kwd>molecular markers</kwd><kwd>long-term spaceflight risks</kwd><kwd>cosmonaut selection</kwd></kwd-group><funding-group><funding-statement xml:lang="ru">обзор выполнен за счет средств, предоставленных для выполнения государственного задания «Изучение состояния здоровья космонавтов, завершивших летную деятельность» (шифр «Долголетие-3»).</funding-statement><funding-statement xml:lang="en">the study was supported by the RSF grant (project № 22-25-20145 “Exploring the Mechanisms Underlying the Effects of Tolerance to Food Antigens on the Glucose Utilization”.</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">Germain A, Kupfer DJ. Circadian rhythm disturbances in depression. Human Psychopharmacology: Clinical and Experimental. 2008; 23 (7): 571–85.</mixed-citation><mixed-citation xml:lang="en">Germain A, Kupfer DJ. Circadian rhythm disturbances in depression. Human Psychopharmacology: Clinical and Experimental. 2008; 23 (7): 571–85.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Johansson C, et al. Circadian clock-related polymorphisms in seasonal affective disorder and their relevance to diurnal preference. Neuropsychopharmacology. 2003; 28 (4): 734–9.</mixed-citation><mixed-citation xml:lang="en">Johansson C, et al. Circadian clock-related polymorphisms in seasonal affective disorder and their relevance to diurnal preference. Neuropsychopharmacology. 2003; 28 (4): 734–9.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Gotlib IH, et al. HPA axis reactivity: a mechanism underlying the associations among 5-HTTLPR, stress, and depression. Biological psychiatry. 2008; 63 (9): 847–51.</mixed-citation><mixed-citation xml:lang="en">Gotlib IH, et al. HPA axis reactivity: a mechanism underlying the associations among 5-HTTLPR, stress, and depression. Biological psychiatry. 2008; 63 (9): 847–51.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Laje G, et al. Genetic markers of suicidal ideation emerging during citalopram treatment of major depression. American Journal of Psychiatry. 2007; 164 (10): 1530–8.</mixed-citation><mixed-citation xml:lang="en">Laje G, et al. Genetic markers of suicidal ideation emerging during citalopram treatment of major depression. American Journal of Psychiatry. 2007; 164 (10): 1530–8.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Hejjas K, et al. Association between depression and the Gln460Arg polymorphism of P2RX7 gene: a dimensional approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 2009; 150 (2): 295–9.</mixed-citation><mixed-citation xml:lang="en">Hejjas K, et al. Association between depression and the Gln460Arg polymorphism of P2RX7 gene: a dimensional approach. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics. 2009; 150 (2): 295–9.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Teper E, O'Brien JT. Vascular factors and depression. International Journal of Geriatric Psychiatry: A journal of the psychiatry of late life and allied sciences. 2008; 23 (10): 993–1000.</mixed-citation><mixed-citation xml:lang="en">Teper E, O'Brien JT. Vascular factors and depression. International Journal of Geriatric Psychiatry: A journal of the psychiatry of late life and allied sciences. 2008; 23 (10): 993–1000.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Germain A, Kupfer DJ. Circadian rhythm disturbances in depression. Human Psychopharmacology: Clinical and Experimental. 2008; 23 (7): 571–85.</mixed-citation><mixed-citation xml:lang="en">Germain A, Kupfer DJ. Circadian rhythm disturbances in depression. Human Psychopharmacology: Clinical and Experimental. 2008; 23 (7): 571–85.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Johansson C, et al. Circadian clock-related polymorphisms in seasonal affective disorder and their relevance to diurnal preference. Neuropsychopharmacology. 2003; 28 (4): 734–9.</mixed-citation><mixed-citation xml:lang="en">Johansson C, et al. Circadian clock-related polymorphisms in seasonal affective disorder and their relevance to diurnal preference. Neuropsychopharmacology. 2003; 28 (4): 734–9.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Goel N, Dinges DF. Predicting risk in space: genetic markers for differential vulnerability to sleep restriction. Acta astronautica. 2012; 77: 207–13.</mixed-citation><mixed-citation xml:lang="en">Goel N, Dinges DF. Predicting risk in space: genetic markers for differential vulnerability to sleep restriction. Acta astronautica. 2012; 77: 207–13.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Goel N, et al. Circadian rhythms, sleep deprivation, and human performance. Progress in molecular biology and translational science. 2013; 119: 155–90.</mixed-citation><mixed-citation xml:lang="en">Goel N, et al. Circadian rhythms, sleep deprivation, and human performance. Progress in molecular biology and translational science. 2013; 119: 155–90.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Dickinson D, Elvevåg B. Genes, cognition and brain through a COMT lens. Neuroscience. 2009; 164 (1): 72–87.</mixed-citation><mixed-citation xml:lang="en">Dickinson D, Elvevåg B. Genes, cognition and brain through a COMT lens. Neuroscience. 2009; 164 (1): 72–87.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Gaedigk A. Complexities of CYP2D6 gene analysis and interpretation. International review of psychiatry. 2013; 25 (5): 534–53.</mixed-citation><mixed-citation xml:lang="en">Gaedigk A. Complexities of CYP2D6 gene analysis and interpretation. International review of psychiatry. 2013; 25 (5): 534–53.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Rudberg I, et al. Impact of the ultrarapid CYP2C19* 17 allele on serum concentration of escitalopram in psychiatric patients. Clinical Pharmacology &amp; Therapeutics. 2008; 83 (2): 322–7.</mixed-citation><mixed-citation xml:lang="en">Rudberg I, et al. Impact of the ultrarapid CYP2C19* 17 allele on serum concentration of escitalopram in psychiatric patients. Clinical Pharmacology &amp; Therapeutics. 2008; 83 (2): 322–7.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Werk AN, Cascorbi I. Functional gene variants of CYP3A. Clinical Pharmacology &amp; Therapeutics. 2014; 96 (3): 340–8.</mixed-citation><mixed-citation xml:lang="en">Werk AN, Cascorbi I. Functional gene variants of CYP3A. Clinical Pharmacology &amp; Therapeutics. 2014; 96 (3): 340–8.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Lee KC, Ma JD, Kuo GM. Pharmacogenomics: bridging the gap between science and practice. Journal of the American Pharmacists Association. 2010; 50 (1): e1-e17.</mixed-citation><mixed-citation xml:lang="en">Lee KC, Ma JD, Kuo GM. Pharmacogenomics: bridging the gap between science and practice. Journal of the American Pharmacists Association. 2010; 50 (1): e1-e17.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Lee SH, et al. Association between the 5‐HT6 receptor C267T polymorphism and response to antidepressant treatment in major depressive disorder. Psychiatry and clinical neurosciences. 2005; 59 (2): 140–5.</mixed-citation><mixed-citation xml:lang="en">Lee SH, et al. Association between the 5‐HT6 receptor C267T polymorphism and response to antidepressant treatment in major depressive disorder. Psychiatry and clinical neurosciences. 2005; 59 (2): 140–5.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Helton SG, Lohoff FW. Serotonin pathway polymorphisms and the treatment of major depressive disorder and anxiety disorders. Pharmacogenomics. 2015; 16 (5): 541–53.</mixed-citation><mixed-citation xml:lang="en">Helton SG, Lohoff FW. Serotonin pathway polymorphisms and the treatment of major depressive disorder and anxiety disorders. Pharmacogenomics. 2015; 16 (5): 541–53.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Vijaya Lakshmi SV, et al. Oxidative stress is associated with genetic polymorphisms in one-carbon metabolism in coronary artery disease. Cell biochemistry and biophysics. 2013; 67: 353–61.</mixed-citation><mixed-citation xml:lang="en">Vijaya Lakshmi SV, et al. Oxidative stress is associated with genetic polymorphisms in one-carbon metabolism in coronary artery disease. Cell biochemistry and biophysics. 2013; 67: 353–61.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Lin H, et al. Gene-gene interaction analyses for atrial fibrillation. Scientific reports. 2016; 6 (1): 35371.</mixed-citation><mixed-citation xml:lang="en">Lin H, et al. Gene-gene interaction analyses for atrial fibrillation. Scientific reports. 2016; 6 (1): 35371.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Eisenberg DTA, Kuzawa CW, Hayes MG. Worldwide allele frequencies of the human apolipoprotein E gene: climate, local adaptations, and evolutionary history.American journal of physical anthropology. 2010; 143 (1): 100–11.</mixed-citation><mixed-citation xml:lang="en">Eisenberg DTA, Kuzawa CW, Hayes MG. Worldwide allele frequencies of the human apolipoprotein E gene: climate, local adaptations, and evolutionary history.American journal of physical anthropology. 2010; 143 (1): 100–11.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Zwart SR, et al. Genotype, B-vitamin status, and androgens affect spaceflight-induced ophthalmic changes. The FASEB Journal. 2016; 30 (1): 141.</mixed-citation><mixed-citation xml:lang="en">Zwart SR, et al. Genotype, B-vitamin status, and androgens affect spaceflight-induced ophthalmic changes. The FASEB Journal. 2016; 30 (1): 141.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Glueck CJ, et al. Idiopathic intracranial hypertension, polycysticovary syndrome, and thrombophilia. Journal of Laboratory and Clinical Medicine. 2005; 145 (2): 72–82.</mixed-citation><mixed-citation xml:lang="en">Glueck CJ, et al. Idiopathic intracranial hypertension, polycysticovary syndrome, and thrombophilia. Journal of Laboratory and Clinical Medicine. 2005; 145 (2): 72–82.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Thompson D, et al. Cancer risks and mortality in heterozygous ATM mutation carriers. Journal of the National Cancer Institute. 2005; 97 (11): 813–22.</mixed-citation><mixed-citation xml:lang="en">Thompson D, et al. Cancer risks and mortality in heterozygous ATM mutation carriers. Journal of the National Cancer Institute. 2005; 97 (11): 813–22.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Yang M, et al. Association of hsp70 polymorphisms with risk of noise-induced hearing loss in Chinese automobile workers. Cell stress &amp; chaperones. 2006; 11 (3): 233.</mixed-citation><mixed-citation xml:lang="en">Yang M, et al. Association of hsp70 polymorphisms with risk of noise-induced hearing loss in Chinese automobile workers. Cell stress &amp; chaperones. 2006; 11 (3): 233.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Konings A, et al. Variations in HSP70 genes associated with noiseinduced hearing loss in two independent populations. European Journal of Human Genetics. 2009; 17 (3): 329–35.</mixed-citation><mixed-citation xml:lang="en">Konings A, et al. Variations in HSP70 genes associated with noiseinduced hearing loss in two independent populations. European Journal of Human Genetics. 2009; 17 (3): 329–35.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Villasana L, et al. Passive avoidance learning and memory of 56Fe sham-irradiated and irradiated human apoE transgenic mice. Radiatsionnaia Biologiia, Radioecologiia. 2008; 48 (2): 167–70.</mixed-citation><mixed-citation xml:lang="en">Villasana L, et al. Passive avoidance learning and memory of 56Fe sham-irradiated and irradiated human apoE transgenic mice. Radiatsionnaia Biologiia, Radioecologiia. 2008; 48 (2): 167–70.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Liu CC, et al. Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy. Nature Reviews Neurology. 2013; 9 (2): 106–18.</mixed-citation><mixed-citation xml:lang="en">Liu CC, et al. Apolipoprotein E and Alzheimer disease: risk, mechanisms and therapy. Nature Reviews Neurology. 2013; 9 (2): 106–18.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Уткин К. В. и др. Установление генетических маркеров устойчивости и чувствительности человека к радиационному воздействию. Иммунология. 2013; 34 (2): 80–4.</mixed-citation><mixed-citation xml:lang="en">Utkin KV, et al. Ustanovlenie geneticheskikh markerov ustoychivosti i chuvstvitel'nosti cheloveka k radiatsionnomu vozdeystviyu. Immunologiya. 2013; 34 (2): 80–4. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Yuan J, et al. Advanced genetic approaches in discovery and characterization of genes involved with osteoporosis in mouse and human. Frontiers in Genetics. 2019; 10: 288.</mixed-citation><mixed-citation xml:lang="en">Yuan J, et al. Advanced genetic approaches in discovery and characterization of genes involved with osteoporosis in mouse and human. Frontiers in Genetics. 2019; 10: 288.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Tan LJ, et al. Molecular genetic studies of gene identification for sarcopenia. Human genetics. 2012; 131: 1–31.</mixed-citation><mixed-citation xml:lang="en">Tan LJ, et al. Molecular genetic studies of gene identification for sarcopenia. Human genetics. 2012; 131: 1–31.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Ralston SH, Uitterlinden AG. Genetics of osteoporosis. Endocrine reviews. 2010; 31 (5): 629–62.</mixed-citation><mixed-citation xml:lang="en">Ralston SH, Uitterlinden AG. Genetics of osteoporosis. Endocrine reviews. 2010; 31 (5): 629–62.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Judex S, et al. Genetic loci that control the loss and regain of trabecular bone during unloading and reambulation. Journal of Bone and Mineral Research. 2013; 28 (7): 1537–49.</mixed-citation><mixed-citation xml:lang="en">Judex S, et al. Genetic loci that control the loss and regain of trabecular bone during unloading and reambulation. Journal of Bone and Mineral Research. 2013; 28 (7): 1537–49.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Shammas MA. Telomeres, lifestyle, cancer, and aging. Current opinion in clinical nutrition and metabolic care. 2011; 14 (1): 28.</mixed-citation><mixed-citation xml:lang="en">Shammas MA. Telomeres, lifestyle, cancer, and aging. Current opinion in clinical nutrition and metabolic care. 2011; 14 (1): 28.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Cawthon RM, et al. Association between telomere length in blood and mortality in people aged 60 years or older. The Lancet. 2003; 361 (9355): 393–5.</mixed-citation><mixed-citation xml:lang="en">Cawthon RM, et al. Association between telomere length in blood and mortality in people aged 60 years or older. The Lancet. 2003; 361 (9355): 393–5.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Wu X, et al. Telomere dysfunction: a potential cancer predisposition factor. Journal of the national cancer institute. 2003; 95 (16): 1211–8.</mixed-citation><mixed-citation xml:lang="en">Wu X, et al. Telomere dysfunction: a potential cancer predisposition factor. Journal of the national cancer institute. 2003; 95 (16): 1211–8.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Epel ES, et al. Accelerated telomere shortening in response to life stress. Proceedings of the National Academy of Sciences. 2004; 101 (49): 17312–5.</mixed-citation><mixed-citation xml:lang="en">Epel ES, et al. Accelerated telomere shortening in response to life stress. Proceedings of the National Academy of Sciences. 2004; 101 (49): 17312–5.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Ayouaz A, et al. Telomeres: hallmarks of radiosensitivity. Biochimie. 2008; 90 (1): 60–72.</mixed-citation><mixed-citation xml:lang="en">Ayouaz A, et al. Telomeres: hallmarks of radiosensitivity. Biochimie. 2008; 90 (1): 60–72.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Grigorev K, et al. Haplotype diversity and sequence heterogeneity of human telomeres. Genome research. 2021; 31 (7): 1269–79.</mixed-citation><mixed-citation xml:lang="en">Grigorev K, et al. Haplotype diversity and sequence heterogeneity of human telomeres. Genome research. 2021; 31 (7): 1269–79.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Luxton JJ, et al. Telomere length dynamics and DNA damage responses associated with long-duration spaceflight. Cell Reports. 2020; 33 (10).</mixed-citation><mixed-citation xml:lang="en">Luxton JJ, et al. Telomere length dynamics and DNA damage responses associated with long-duration spaceflight. Cell Reports. 2020; 33 (10).</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Nishi H, et al. Hypoxia-inducible factor 1 mediates upregulation of telomerase (hTERT). Molecular and cellular biology. 2004; 24 (13): 6076–83.</mixed-citation><mixed-citation xml:lang="en">Nishi H, et al. Hypoxia-inducible factor 1 mediates upregulation of telomerase (hTERT). Molecular and cellular biology. 2004; 24 (13): 6076–83.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Bezdan D, et al. Cell-free DNA (cfDNA) and exosome profiling from a year-long human spaceflight reveals circulating biomarkers. Iscience. 2020; 23 (12).</mixed-citation><mixed-citation xml:lang="en">Bezdan D, et al. Cell-free DNA (cfDNA) and exosome profiling from a year-long human spaceflight reveals circulating biomarkers. Iscience. 2020; 23 (12).</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Snyder MW, et al. Cell-free DNA comprises an in vivo nucleosome footprint that informs its tissues-of-origin. Cell. 2016; 164 (1): 57–68.</mixed-citation><mixed-citation xml:lang="en">Snyder MW, et al. Cell-free DNA comprises an in vivo nucleosome footprint that informs its tissues-of-origin. Cell. 2016; 164 (1): 57–68.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Yoshioka Y, et al. Ultra-sensitive liquid biopsy of circulating extracellular vesicles using ExoScreen. Nature communications. 2014; 5 (1): 3591.</mixed-citation><mixed-citation xml:lang="en">Yoshioka Y, et al. Ultra-sensitive liquid biopsy of circulating extracellular vesicles using ExoScreen. Nature communications. 2014; 5 (1): 3591.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Hoshino A, et al. Tumour exosome integrins determine organotropic metastasis. Nature. 2015; 527 (7578): 329–35.</mixed-citation><mixed-citation xml:lang="en">Hoshino A, et al. Tumour exosome integrins determine organotropic metastasis. Nature. 2015; 527 (7578): 329–35.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Kumar Deshmukh F, et al. The contribution of the 20S proteasome to proteostasis. Biomolecules. 2019; 9 (5): 190.</mixed-citation><mixed-citation xml:lang="en">Kumar Deshmukh F, et al. The contribution of the 20S proteasome to proteostasis. Biomolecules. 2019; 9 (5): 190.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Кудряева А. А., Белогуров А. А. Протеасома: наномашинерия созидательного разрушения. Биохимия. 2019; 84: 159–92.</mixed-citation><mixed-citation xml:lang="en">Kudriaeva AA, Belogurov AA. Proteasome: a Nanomachinery of Creative Destruction. Biochemistry. 2019; 84: 159–92. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Alvarez R, et al. A simulated microgravity environment causes a sustained defect in epithelial barrier function. Scientific reports. 2019; 9 (1): 17531.</mixed-citation><mixed-citation xml:lang="en">Alvarez R, et al. A simulated microgravity environment causes a sustained defect in epithelial barrier function. Scientific reports. 2019; 9 (1): 17531.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Mencia-Trinchant N, et al. Clonal hematopoiesis before, during, and after human spaceflight. Cell reports. 2020; 33 (10).</mixed-citation><mixed-citation xml:lang="en">Mencia-Trinchant N, et al. Clonal hematopoiesis before, during, and after human spaceflight. Cell reports. 2020; 33 (10).</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Genovese G, et al. Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence. New England Journal of Medicine. 2014; 371 (26): 2477–87.</mixed-citation><mixed-citation xml:lang="en">Genovese G, et al. Clonal hematopoiesis and blood-cancer risk inferred from blood DNA sequence. New England Journal of Medicine. 2014; 371 (26): 2477–87.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Пастушкова Л. Х. и др. Изменения протеома крови космонавтов с микро- и макрососудистыми травмами при перегрузках на заключительном этапе длительных космических полетов. Авиакосмическая и экологическая медицина. 2020; 54 (5): 5–14.</mixed-citation><mixed-citation xml:lang="en">Pastushkova LKh, et al. Changes in blood proteome of cosmonauts with microand macrovascular injuries due to g-loads at the final stage of long-duration space missions. Aviakosmicheskaya i Ekologicheskaya Meditsina. 2020; 54 (5): 5–14. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Каширина Д. Н. и др. Изменение белкового состава плазмы космонавтов после космического полета и его значение для функций эндотелия. Физиология человека. 2019; 45 (1): 88–96.</mixed-citation><mixed-citation xml:lang="en">Kashirina DN, et al. Changes in the Plasma Protein Composition in Astronauts after Space Flight and its Significance for Endothelial Functions. Human Physiology. 2019; 45 (1): 88–96. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Моруков Б. В. и др. Показатели врожденного и адаптивного иммунитета у космонавтов после длительных космических полетов на Международной космической станции. Физиология человека. 2010; 36 (3): 19–30.</mixed-citation><mixed-citation xml:lang="en">Morukov VB, et al. Indicators of innate and adaptive immunity of cosmonauts after long-term space flight to international space station. Human Physiology. 2010; 36 (3): 19–30. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Рыкова М. П. Иммунная система у российских космонавтов после орбитальных полетов. Физиология человека. 2013; 39 (5): 126–126.</mixed-citation><mixed-citation xml:lang="en">Rykova MP. Immune system in Russian cosmonauts after orbital space flights. Human Physiology. 2013; 39 (5): 126–126. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Новиков В. Е. и др. Минеральная плотность костной ткани и молекулярно-генетические маркеры ее ремоделирования в крови у космонавтов после длительных полетов на международной космической станции. Физиология человека. 2017; 43 (6): 88–94.</mixed-citation><mixed-citation xml:lang="en">Novikov VE, et al. Mineral'naya plotnost' kostnoy tkani i molekulyarno-geneticheskie markery ee remodelirovaniya v krovi u kosmonavtov posle dlitel'nykh poletov na mezhdunarodnoy kosmicheskoy stantsii. Human Physiology. 2017; 43 (6): 88–94. Russian.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Сапецкий А. О. и др. Радиационная нейробиология дальних космических полетов. Успехи современной биологии. 2017; 137 (2): 165–94.</mixed-citation><mixed-citation xml:lang="en">Sapetsky AO, et al. Radiation neurobiology of long-term space flights. Biology Bulletin Reviews. 2017; 137 (2): 165–94. Russian.</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>
