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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">surgonco</journal-id><journal-title-group><journal-title xml:lang="ru">Креативная хирургия и онкология</journal-title><trans-title-group xml:lang="en"><trans-title>Creative surgery and oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2076-3093</issn><issn pub-type="epub">2307-0501</issn><publisher><publisher-name>Башкирский государственный медицинский университет</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.24060/2076-3093-2021-11-2-183-187</article-id><article-id custom-type="elpub" pub-id-type="custom">surgonco-589</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 ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group></article-categories><title-group><article-title>Прогностическое значение мутаций в генах BRCA1 и BRCA2 при раке предстательной железы (обзор литературы)</article-title><trans-title-group xml:lang="en"><trans-title>Prognostic Value of BRCA1 and BRCA2 Gene Mutations in Prostate Cancer: a Literature 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/0000-0002-1550-6069</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Логинова</surname><given-names>М. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Loginova</surname><given-names>M. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Логинова Мария Владиславовна — онкологическое отделение противоопухолевой лекарственной терапии, кафедра урологии с курсом ИДПО, +7 (937) 166-14-08</p><p>Россия, Республика Башкортостан, Уфа</p><p> </p></bio><bio xml:lang="en"><p>Maria V. Loginova — Anticancer Drug Therapy Unit, Department of Urology with a course of Advanced Professional Education</p><p>Ufa, Russian Federation</p></bio><email xlink:type="simple">mariialoginova25@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2125-4897</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Павлов</surname><given-names>В. Н.</given-names></name><name name-style="western" xml:lang="en"><surname>Pavlov</surname><given-names>V. N.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Павлов Валентин Николаевич — д.м.н., профессор, член-корр. РАН, кафедра урологии с курсом ИДПО</p><p>Россия, Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Valentin N. Pavlov — Dr. Sci. (Med.), Prof., Corresponding Member of the Russian Academy of Sciences, Department of Urology with a course of Advanced Professional Education</p><p>Ufa, Russian Federation</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-9499-5632</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гилязова</surname><given-names>И. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Gilyazova</surname><given-names>I. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гилязова Ирина Ришатовна — к.б.н., кафедра медицинской генетики и фундаментальной медицины, лаборатория молекулярной генетики человека</p><p>Россия, Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Irina R. Gilyazova — Cand. Sci. (Biol.), Department of Medical Genetics and Fundamental Medicine, Laboratory of Human Molecular Genetics</p><p>Ufa, Russian Federation</p></bio><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>Республиканский клинический онкологический диспансер; Башкирский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Republican Clinical Oncological Dispensary; Bashkir State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-2"><aff xml:lang="ru"><institution>Башкирский государственный медицинский университет</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Bashkir State Medical University</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Институт биохимии и генетики Уфимского федерального исследовательского центра РАН</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Institute of Biochemistry and Genetics of Ufa Federal Research Centre of the Russian Academy of Sciences</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2021</year></pub-date><pub-date pub-type="epub"><day>22</day><month>05</month><year>2021</year></pub-date><volume>11</volume><issue>2</issue><fpage>183</fpage><lpage>187</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Логинова М.В., Павлов В.Н., Гилязова И.Р., 2021</copyright-statement><copyright-year>2021</copyright-year><copyright-holder xml:lang="ru">Логинова М.В., Павлов В.Н., Гилязова И.Р.</copyright-holder><copyright-holder xml:lang="en">Loginova M.V., Pavlov V.N., Gilyazova I.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.surgonco.ru/jour/article/view/589">https://www.surgonco.ru/jour/article/view/589</self-uri><abstract><p>Во всем мире наблюдается значительный рост злокачественных новообразований предстательной железы. Большое количество пациентов на момент выявления заболевания являются неоперабельными. Выбор правильной тактики лечения является сложной задачей на сегодняшний день. Метастатический кастрационно-резистентный рак предстательной железы в настоящее время остается смертельным заболеванием с плохим прогнозом, но с каждым годом список химиотерапевтических препаратов и ингибиторов передачи сигналов андрогеновых рецепторов расширяется и достигаются определенные успехи в лечении пациентов с данным заболеванием. Многочисленные исследования показывают, что во многих случаях неблагоприятный прогноз у пациентов связан с герминальными мутациями или приобретенными дефектами в генах репарации ДНК. Среди дефектов ДНК мутации в генах BRCA1 и BRCA2 имеют важные клинические последствия для исхода заболевания у пациента. Мутации в этих генах связаны с неблагоприятными клиническими проявлениями в первичных опухолях и с плохими результатами лечения у пациентов с метастатическим кастрационно-резистентным раком предстательной железы. В данном обзоре делается попытка описать мутации в генах BRCA1/2 при раке предстательной железы, сосредоточив внимание на их прогностической роли.</p></abstract><trans-abstract xml:lang="en"><p>Prostate malignancies aggressively grow worldwide frequently occurring inoperable at diagnosis. A proper choice of treatment strategy is currently a challenge. Metastatic castration-resistant prostate cancer remains fatal and poor-prognosis, albeit the list of chemotherapeutic agents and androgen receptor signalling inhibitors has recently been extending towards a certain therapeutic success. Numerous studies suggest a frequent association of the unfavourable prognosis with germline or somatic damage of DNA repair genes. Such are mutations in the BRCA1 and BRCA2 genes bearing important clinical implications for the patient outcome through an adverse clinical manifest of primary tumours and poor treatment in metastatic castration-resistant prostate cancer. This review attempts to describe the BRCA1/2 mutations in prostate cancer with a focus on their prognostic value.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>рак предстательной железы</kwd><kwd>гены BRCA1</kwd><kwd>гены BRCA2</kwd><kwd>метастатический кастрационно-резистентный рак</kwd><kwd>ДНК репарация</kwd><kwd>мутация</kwd><kwd>зародышевой линии мутация</kwd></kwd-group><kwd-group xml:lang="en"><kwd>prostate cancer</kwd><kwd>BRCA1 gene</kwd><kwd>BRCA2 gene</kwd><kwd>metastatic castration-resistant cancer</kwd><kwd>DNA repair</kwd><kwd>mutation</kwd><kwd>germline mutation</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">Fitzmaurice C., Allen C., Barber R.M., Barregard L., Bhutta A.Z., Brenner H., et al. Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted lifeyears for 32 cancer groups, 1990 to 2015: a systematic analysis for the global burden of disease study. JAMA Oncol. 2017;3(4):524–48. DOI: 10.1001/jamaoncol.2016.5688</mixed-citation><mixed-citation xml:lang="en">Fitzmaurice C., Allen C., Barber R.M., Barregard L., Bhutta A.Z., Brenner H., et al. Global, regional, and national cancer incidence, mortality, years of life lost, years lived with disability, and disability-adjusted lifeyears for 32 cancer groups, 1990 to 2015: a systematic analysis for the global burden of disease study. JAMA Oncol. 2017;3(4):524–48. DOI: 10.1001/jamaoncol.2016.5688</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Siegel R.L., Miller K.D., Jemal A. Cancer statistics, 2018. CA: A Cancer J Clin. 2018;68(1):7–30. DOI: 10.3322/caac.21442</mixed-citation><mixed-citation xml:lang="en">Siegel R.L., Miller K.D., Jemal A. Cancer statistics, 2018. CA: A Cancer J Clin. 2018;68(1):7–30. DOI: 10.3322/caac.21442</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">James N.D., Sydes M.R., Clarke N.W., Mason M., Dearnaley D., Spears M., et al. Addition of docetaxel, zoledronic acid, or both to first-line long-term hormone therapy in prostate cancer (STAMPEDE): survival results from an adaptive, multiarm, multistage, platform randomised controlled trial. Lancet. 2016;387(10024):1163–77. DOI: 10.1016/s0140-6736(15)01037-5</mixed-citation><mixed-citation xml:lang="en">James N.D., Sydes M.R., Clarke N.W., Mason M., Dearnaley D., Spears M., et al. Addition of docetaxel, zoledronic acid, or both to first-line long-term hormone therapy in prostate cancer (STAMPEDE): survival results from an adaptive, multiarm, multistage, platform randomised controlled trial. Lancet. 2016;387(10024):1163–77. DOI: 10.1016/s0140-6736(15)01037-5</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Gillessen S., Omlin A., Attard G., Bono J., Efstathiou E., Fizazi K., et al. Management of patients with advanced prostate cancer: recommendations of the St Gallen Advanced Prostate Cancer Consensus Conference (APCCC) 2015. Ann Oncol. 2015;26(8):1589–604. DOI: 10.1093/annonc/mdv257</mixed-citation><mixed-citation xml:lang="en">Gillessen S., Omlin A., Attard G., Bono J., Efstathiou E., Fizazi K., et al. Management of patients with advanced prostate cancer: recommendations of the St Gallen Advanced Prostate Cancer Consensus Conference (APCCC) 2015. Ann Oncol. 2015;26(8):1589–604. DOI: 10.1093/annonc/mdv257</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Byrski T., Gronwald J., Huzarski T., Grzybowska E., Budryk M., Stawicka M., et al. Pathologic complete response rates in young women with BRCA1-positive breast cancers after neoadjuvant chemotherapy. J Clin Oncol. 2010;28(3):375–9. DOI: 10.1200/JCO.2008.20.7019</mixed-citation><mixed-citation xml:lang="en">Byrski T., Gronwald J., Huzarski T., Grzybowska E., Budryk M., Stawicka M., et al. Pathologic complete response rates in young women with BRCA1-positive breast cancers after neoadjuvant chemotherapy. J Clin Oncol. 2010;28(3):375–9. DOI: 10.1200/JCO.2008.20.7019</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Mucci L.A., Hjelmborg J.B., Harris J.R., Czene K., Havelick D, Scheikeet T., et al. Familial risk and heritability of cancer among twins in Nordic Countries. JAMA. 2016;315(1):68–76. DOI: 10.1001/jama.2015.17703</mixed-citation><mixed-citation xml:lang="en">Mucci L.A., Hjelmborg J.B., Harris J.R., Czene K., Havelick D, Scheikeet T., et al. Familial risk and heritability of cancer among twins in Nordic Countries. JAMA. 2016;315(1):68–76. DOI: 10.1001/jama.2015.17703</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Robinson D., Van Allen E.M., Wu Y.M., Schultz N., Lonigro R., Mosquera J-M., et al. Integrative clinical genomics of advanced prostate cancer. Cell. 2015;162(2):454. DOI: 10.1016/j.cell.2015.06.053</mixed-citation><mixed-citation xml:lang="en">Robinson D., Van Allen E.M., Wu Y.M., Schultz N., Lonigro R., Mosquera J-M., et al. Integrative clinical genomics of advanced prostate cancer. Cell. 2015;162(2):454. DOI: 10.1016/j.cell.2015.06.053</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Kote-Jarai Z., Leongamornlert D., Saunders E., Tymrakiewicz M., Castro E., Mahmud N., et al. BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients. Br J Cancer. 2011;105(8):1230–4. DOI: 10.1038/bjc.2011.383</mixed-citation><mixed-citation xml:lang="en">Kote-Jarai Z., Leongamornlert D., Saunders E., Tymrakiewicz M., Castro E., Mahmud N., et al. BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients. Br J Cancer. 2011;105(8):1230–4. DOI: 10.1038/bjc.2011.383</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Eeles R., Goh C., Castro E., Bancroft E., Guy M., Olama A., et al. The genetic epidemiology of prostate cancer and its clinical implications. Nat Rev Urol. 2014;11(1):18–31. DOI: 10.1038/nrurol.2013.266</mixed-citation><mixed-citation xml:lang="en">Eeles R., Goh C., Castro E., Bancroft E., Guy M., Olama A., et al. The genetic epidemiology of prostate cancer and its clinical implications. Nat Rev Urol. 2014;11(1):18–31. DOI: 10.1038/nrurol.2013.266</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Reinhardt H.C., Yaffe M.B. Phospho-Ser/Thr-binding domains: navigating the cell cycle and DNA damage response. Nat Rev Mol Cell Biol. 2013;14(9):563–80. DOI: 10.1038/nrm3640</mixed-citation><mixed-citation xml:lang="en">Reinhardt H.C., Yaffe M.B. Phospho-Ser/Thr-binding domains: navigating the cell cycle and DNA damage response. Nat Rev Mol Cell Biol. 2013;14(9):563–80. DOI: 10.1038/nrm3640</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Sáez G.T. DNA Injury and Repair Systems. Int J Mol Sci. 2018;19(7):1902. DOI: 10.3390/ijms19071902</mixed-citation><mixed-citation xml:lang="en">Sáez G.T. DNA Injury and Repair Systems. Int J Mol Sci. 2018;19(7):1902. DOI: 10.3390/ijms19071902</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Reinhardt H.C., Schumacher B. The p53 network: cellular and systemic DNA damage responses in aging and cancer. Trends Genet. 2012;28(3):128–36. DOI: 10.1016/j.tig.2011.12.002</mixed-citation><mixed-citation xml:lang="en">Reinhardt H.C., Schumacher B. The p53 network: cellular and systemic DNA damage responses in aging and cancer. Trends Genet. 2012;28(3):128–36. DOI: 10.1016/j.tig.2011.12.002</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Dietlein F., Thelen L., Reinhardt H.C. Cancer-specific defects in DNA repair pathways as targets for personalized therapeutic approaches. Trends Genet. 2014;30(8):326–39. DOI: 10.1016/j.tig.2014.06.003</mixed-citation><mixed-citation xml:lang="en">Dietlein F., Thelen L., Reinhardt H.C. Cancer-specific defects in DNA repair pathways as targets for personalized therapeutic approaches. Trends Genet. 2014;30(8):326–39. DOI: 10.1016/j.tig.2014.06.003</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Yu K., Shao Z. Initiation, evolution, phenotype and outcome of BRCA1 and BRCA2 mutation-associated breast cancer. Nat Rev Cancer. 2012;12(5):372–3. DOI: 10.1038/nrc3181-c1</mixed-citation><mixed-citation xml:lang="en">Yu K., Shao Z. Initiation, evolution, phenotype and outcome of BRCA1 and BRCA2 mutation-associated breast cancer. Nat Rev Cancer. 2012;12(5):372–3. DOI: 10.1038/nrc3181-c1</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Castro E., Goh C., Olmos D., Saunders E., Leongamornlert D., Tymrakiewicz M., et al. Germline BRCA mutations are associated with</mixed-citation><mixed-citation xml:lang="en">Castro E., Goh C., Olmos D., Saunders E., Leongamornlert D., Tymrakiewicz M., et al. Germline BRCA mutations are associated with</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer. J Clin Oncol. 2013;31(14):1748–57. DOI: 10.1200/jco.2012.43.1882</mixed-citation><mixed-citation xml:lang="en">higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer. J Clin Oncol. 2013;31(14):1748–57. DOI: 10.1200/jco.2012.43.1882</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Antonarakis E.S., Lu C., Luber B., Liang C., Wang H., Chen Y., et al. Germline DNArepair gene mutations and outcomes in men with metastatic castration-resistant prostate cancer receiving first-line abiraterone and enzalutamide. Eur Urol. 2018;74(2):218–25. DOI: 10.1016/j.eururo.2018.01.035</mixed-citation><mixed-citation xml:lang="en">Antonarakis E.S., Lu C., Luber B., Liang C., Wang H., Chen Y., et al. Germline DNArepair gene mutations and outcomes in men with metastatic castration-resistant prostate cancer receiving first-line abiraterone and enzalutamide. Eur Urol. 2018;74(2):218–25. DOI: 10.1016/j.eururo.2018.01.035</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Mateo J., Carreira S., Sandhu S., Miranda S., Mossop H., Perez-Lopez R., et al. DNA-repair defects and olaparib in metastatic prostate cancer. New Engl J Med. 2015;373(18):1697–708. DOI: 10.1056/NEJMoa1506859</mixed-citation><mixed-citation xml:lang="en">Mateo J., Carreira S., Sandhu S., Miranda S., Mossop H., Perez-Lopez R., et al. DNA-repair defects and olaparib in metastatic prostate cancer. New Engl J Med. 2015;373(18):1697–708. DOI: 10.1056/NEJMoa1506859</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Abeshouse A., Ahn J., Akbani R. Molecular taxonomy of primary prostate cancer. Cell. 2015;163(4):1011–25. DOI: 10.1038/s41598-017-00872-8</mixed-citation><mixed-citation xml:lang="en">Abeshouse A., Ahn J., Akbani R. Molecular taxonomy of primary prostate cancer. Cell. 2015;163(4):1011–25. DOI: 10.1038/s41598-017-00872-8</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Pritchard C.C., Mateo J., Walsh M.F., Sarkar N., Abida W., Beltran H., et al. Inherited DNA-repair gene mutations in men with metastatic prostate cancer. New Engl J Med. 2016;375(5):443–53. DOI: 10.1056/NEJMoa1603144</mixed-citation><mixed-citation xml:lang="en">Pritchard C.C., Mateo J., Walsh M.F., Sarkar N., Abida W., Beltran H., et al. Inherited DNA-repair gene mutations in men with metastatic prostate cancer. New Engl J Med. 2016;375(5):443–53. DOI: 10.1056/NEJMoa1603144</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Leongamornlert D., Mahmud N., Tymrakiewicz M., Saunders E., Dadaev T., Castroet E., et al. Germline BRCA1 mutations increase prostate cancer risk. Br J Cancer. 2012;106:1697–701. DOI:10.1038/bjc.2012.146</mixed-citation><mixed-citation xml:lang="en">Leongamornlert D., Mahmud N., Tymrakiewicz M., Saunders E., Dadaev T., Castroet E., et al. Germline BRCA1 mutations increase prostate cancer risk. Br J Cancer. 2012;106:1697–701. DOI:10.1038/bjc.2012.146</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Cybulski C., Wokolorczyk D., Kluzniak W., Jakubowska A., Górski B., Gronwald J., et al. An inherited NBN mutation is associated with poor prognosis prostate cancer. Br J Cancer. 2013;108:461–8. DOI: 10.1038/bjc.2012.486</mixed-citation><mixed-citation xml:lang="en">Cybulski C., Wokolorczyk D., Kluzniak W., Jakubowska A., Górski B., Gronwald J., et al. An inherited NBN mutation is associated with poor prognosis prostate cancer. Br J Cancer. 2013;108:461–8. DOI: 10.1038/bjc.2012.486</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Lazzeri M., Lughezzani G. Inherited DNA-repair gene mutations in men with metastatic prostate cancer. Eur Urol. 2016;70(4):703–4. DOI: 10.1016/j.eururo.2016.07.039</mixed-citation><mixed-citation xml:lang="en">Lazzeri M., Lughezzani G. Inherited DNA-repair gene mutations in men with metastatic prostate cancer. Eur Urol. 2016;70(4):703–4. DOI: 10.1016/j.eururo.2016.07.039</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Mersch J., Jackson M.A., Park M., Nebgen D., Peterson S., Singletary C., et al. Cancers associated with BRCA1 and BRCA2 mutations other than breast and ovarian. Cancer 2015;121:269–75. DOI: 10.1002/cncr.29041</mixed-citation><mixed-citation xml:lang="en">Mersch J., Jackson M.A., Park M., Nebgen D., Peterson S., Singletary C., et al. Cancers associated with BRCA1 and BRCA2 mutations other than breast and ovarian. Cancer 2015;121:269–75. DOI: 10.1002/cncr.29041</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Mayor S. Third of men with treatment resistant prostate cancer respond to drug that targets gene defect, study finds. BMJ. 2015;351:5783. DOI: 10.1136/bmj.h5783</mixed-citation><mixed-citation xml:lang="en">Mayor S. Third of men with treatment resistant prostate cancer respond to drug that targets gene defect, study finds. BMJ. 2015;351:5783. DOI: 10.1136/bmj.h5783</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Moran A., O’Hara C., Khan S., Shack L., Woodward E., Maher E.R., et al. Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations. Fam Cancer 2012;11:235–42. DOI: 10.1007/s10689-011-9506-2</mixed-citation><mixed-citation xml:lang="en">Moran A., O’Hara C., Khan S., Shack L., Woodward E., Maher E.R., et al. Risk of cancer other than breast or ovarian in individuals with BRCA1 and BRCA2 mutations. Fam Cancer 2012;11:235–42. DOI: 10.1007/s10689-011-9506-2</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Mullane S.A., Van Allen E.M. Precision medicine for advanced prostate cancer. Curr Opin Urol. 2016;26(3):231–9. DOI: 10.1097/MOU.0000000000000278</mixed-citation><mixed-citation xml:lang="en">Mullane S.A., Van Allen E.M. Precision medicine for advanced prostate cancer. Curr Opin Urol. 2016;26(3):231–9. DOI: 10.1097/MOU.0000000000000278</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Nombela P., Lozano R., Aytes A., Mateo J., Olmos D., Castro E., et al. BRCA2 and other DDR genes in prostate cancer. Cancers (Basel). 2019;11(3):352. DOI: 10.3390/cancers11030352</mixed-citation><mixed-citation xml:lang="en">Nombela P., Lozano R., Aytes A., Mateo J., Olmos D., Castro E., et al. BRCA2 and other DDR genes in prostate cancer. Cancers (Basel). 2019;11(3):352. DOI: 10.3390/cancers11030352</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Castro E., Goh C., Leongamornlert D., Saunders E., Tymrakiewicz M., Dadaev T., et al. Effect of BRCA mutations on metastatic relapse and cause-specific survival after radical treatment for localised prostate cancer. Eur Urol. 2015;68(2):186–93. DOI: 10.1016/j.eururo.2014.10.022</mixed-citation><mixed-citation xml:lang="en">Castro E., Goh C., Leongamornlert D., Saunders E., Tymrakiewicz M., Dadaev T., et al. Effect of BRCA mutations on metastatic relapse and cause-specific survival after radical treatment for localised prostate cancer. Eur Urol. 2015;68(2):186–93. DOI: 10.1016/j.eururo.2014.10.022</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Roy R., Chun J., Powell S.N. BRCA1 and BRCA2: different roles in a common pathway of genome protection. Nat Rev Cancer. 2011;12 (1):68–78. DOI: 10.1038/nrc3181</mixed-citation><mixed-citation xml:lang="en">Roy R., Chun J., Powell S.N. BRCA1 and BRCA2: different roles in a common pathway of genome protection. Nat Rev Cancer. 2011;12 (1):68–78. DOI: 10.1038/nrc3181</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Zafeiriou Z., Bianchini D., Chandler R., Rescigno P., Yuan W., Carreiraet S., et al. Genomic analysis of three metastatic prostate cancer patients with exceptional responses to carboplatin indicating different types of DNA repair deficiency. Eur Urol. 2019.75(1):184–92. DOI: 10.1016/j.eururo.2018.09.048</mixed-citation><mixed-citation xml:lang="en">Zafeiriou Z., Bianchini D., Chandler R., Rescigno P., Yuan W., Carreiraet S., et al. Genomic analysis of three metastatic prostate cancer patients with exceptional responses to carboplatin indicating different types of DNA repair deficiency. Eur Urol. 2019.75(1):184–92. DOI: 10.1016/j.eururo.2018.09.048</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Annala M., Struss W.J., Warner E.W., Beja K., Vandekerkhove G., Wong A., et al. Treatment outcomes and tumor loss of heterozygosity in germline DNA repair-deficient prostate cancer. Eur Urol. 2017;72(1):34–42. DOI: 10.1016/j.eururo.2017.02.023</mixed-citation><mixed-citation xml:lang="en">Annala M., Struss W.J., Warner E.W., Beja K., Vandekerkhove G., Wong A., et al. Treatment outcomes and tumor loss of heterozygosity in germline DNA repair-deficient prostate cancer. Eur Urol. 2017;72(1):34–42. DOI: 10.1016/j.eururo.2017.02.023</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Young G.J., Harrison S., Turner E.L., Walsh E., Oliver S., Ben- Shlomoet Y., et al. Prostate-specific antigen (PSA) testing of men in UK general practice: a 10-year longitudinal cohort study. BMJ Open. 2017;7:e017729. DOI: 10.1136/bmjopen-2017-017729</mixed-citation><mixed-citation xml:lang="en">Young G.J., Harrison S., Turner E.L., Walsh E., Oliver S., Ben- Shlomoet Y., et al. Prostate-specific antigen (PSA) testing of men in UK general practice: a 10-year longitudinal cohort study. BMJ Open. 2017;7:e017729. DOI: 10.1136/bmjopen-2017-017729</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Fachal L., Gomez-Caamano A., Celeiro-Munoz C., Peleteiro P., Blanco A., Carballo A., et al. BRCA1 mutations do not increase prostate cancer risk: results from a metaanalysis including new data. Prostate. 2011;71:1768–79. DOI: 10.1002/pros.21394</mixed-citation><mixed-citation xml:lang="en">Fachal L., Gomez-Caamano A., Celeiro-Munoz C., Peleteiro P., Blanco A., Carballo A., et al. BRCA1 mutations do not increase prostate cancer risk: results from a metaanalysis including new data. Prostate. 2011;71:1768–79. DOI: 10.1002/pros.21394</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Laitman Y., Boker K.L., Liphsitz I., Weissglas-Volkov D., Litz-Philipsborn S., Schayek H., et al. Cancer risks in Jewish male BRCA1 and BRCA2 mutation carriers. Breast Cancer Res Treat. 2015;150:631–5. DOI: 10.1007/s10549-015-3340-4</mixed-citation><mixed-citation xml:lang="en">Laitman Y., Boker K.L., Liphsitz I., Weissglas-Volkov D., Litz-Philipsborn S., Schayek H., et al. Cancer risks in Jewish male BRCA1 and BRCA2 mutation carriers. Breast Cancer Res Treat. 2015;150:631–5. DOI: 10.1007/s10549-015-3340-4</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Loeb L.A. Human cancers express a mutator phenotype: hypothesis, origin, and consequences. Cancer Res. 2016;76(8):2057–9. DOI: 10.1158/0008-5472.CAN-16-0794</mixed-citation><mixed-citation xml:lang="en">Loeb L.A. Human cancers express a mutator phenotype: hypothesis, origin, and consequences. Cancer Res. 2016;76(8):2057–9. DOI: 10.1158/0008-5472.CAN-16-0794</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Giri V.N., Knudsen K.E., Kelly W.K., Cheng H., Cooney K., Cookson M., et al. Implementation of germline testing for prostate cancer: Philadelphia prostate cancer consensus conference 2019. J Clin Oncol. 2020;38(24):2798–811. DOI: 10.1200/JCO.20.00046</mixed-citation><mixed-citation xml:lang="en">Giri V.N., Knudsen K.E., Kelly W.K., Cheng H., Cooney K., Cookson M., et al. Implementation of germline testing for prostate cancer: Philadelphia prostate cancer consensus conference 2019. J Clin Oncol. 2020;38(24):2798–811. DOI: 10.1200/JCO.20.00046</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Carroll P.R., Parsons J.K., Andriole G., Bahnson R.R., Castle E.P., Catalona W.J., et al. NCCN Guidelines Insights: prostate cancer early detection, version 2.2016. J Natl Compr Canc Netw. 2016;14(5):509–19. DOI: 10.6004/jnccn.2016.0060</mixed-citation><mixed-citation xml:lang="en">Carroll P.R., Parsons J.K., Andriole G., Bahnson R.R., Castle E.P., Catalona W.J., et al. NCCN Guidelines Insights: prostate cancer early detection, version 2.2016. J Natl Compr Canc Netw. 2016;14(5):509–19. DOI: 10.6004/jnccn.2016.0060</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Smith M.R., Sandhu S.K., Kelly W.K., Scher H.I., Efstathiou E., Lara P.N., et al. LBA50 — Pre-specified interim analysis of GALAHAD: a phase II study of niraparib in patients (pts) with metastatic castration- resistant prostate cancer (mCRPC) and biallelic DNA-repair gene defects (DRD). Ann Oncol. 2019;30(5):884–5. DOI: 10.1158/1078-0432.ccr-20-0394</mixed-citation><mixed-citation xml:lang="en">Smith M.R., Sandhu S.K., Kelly W.K., Scher H.I., Efstathiou E., Lara P.N., et al. LBA50 — Pre-specified interim analysis of GALAHAD: a phase II study of niraparib in patients (pts) with metastatic castration- resistant prostate cancer (mCRPC) and biallelic DNA-repair gene defects (DRD). Ann Oncol. 2019;30(5):884–5. DOI: 10.1158/1078-0432.ccr-20-0394</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Parker C., Castro E., Fizazi K., Heidenreich A., Ost P., Procopio G., et al. On behalf of the ESMO guidelines commitee, prostate cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2020;31(9):1119–34. DOI: 10.1016/j.annonc.2020.06.011</mixed-citation><mixed-citation xml:lang="en">Parker C., Castro E., Fizazi K., Heidenreich A., Ost P., Procopio G., et al. On behalf of the ESMO guidelines commitee, prostate cancer: ESMO clinical practice guidelines for diagnosis, treatment and follow-up. Ann Oncol. 2020;31(9):1119–34. DOI: 10.1016/j.annonc.2020.06.011</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Bancroft E.K., Page E.C., Castro E., Lilja H., Vickerset A., Sjoberg D., et al. Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study. Eur Urol. 2014;66(3):489–99. DOI: 10.1016/j.eururo.2014.01.003</mixed-citation><mixed-citation xml:lang="en">Bancroft E.K., Page E.C., Castro E., Lilja H., Vickerset A., Sjoberg D., et al. Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study. Eur Urol. 2014;66(3):489–99. DOI: 10.1016/j.eururo.2014.01.003</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Draisma G., Boer R., Otto S.J., van der Cruijsen I.W., Damhuis R.A., Schröder F.H., et al. Lead times and overdetection due to prostatespecific antigen screening: estimates from the European Randomized Study of Screening for Prostate Cancer. J Natl Cancer Inst. 2003;95(12):868–78. DOI: 10.1093/jnci/95.12.868</mixed-citation><mixed-citation xml:lang="en">Draisma G., Boer R., Otto S.J., van der Cruijsen I.W., Damhuis R.A., Schröder F.H., et al. Lead times and overdetection due to prostatespecific antigen screening: estimates from the European Randomized Study of Screening for Prostate Cancer. J Natl Cancer Inst. 2003;95(12):868–78. DOI: 10.1093/jnci/95.12.868</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Lecarpentier J., Silvestri V., Kuchenbaecker K.B., Barrowdale D., Dennis J., McGuffog L., et al. Prediction of breast and prostate cancer risks in male BRCA1 and BRCA2 mutation carriers using polygenic risk scores. J Clin Oncol. 2017;35:2240–50. DOI: 10.1200/JCO.2016.69.4935</mixed-citation><mixed-citation xml:lang="en">Lecarpentier J., Silvestri V., Kuchenbaecker K.B., Barrowdale D., Dennis J., McGuffog L., et al. Prediction of breast and prostate cancer risks in male BRCA1 and BRCA2 mutation carriers using polygenic risk scores. J Clin Oncol. 2017;35:2240–50. DOI: 10.1200/JCO.2016.69.4935</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Mohler J.L., Antonarakis E.S., Armstrong A.J., D’Amico A.V., Davis B.J., Dorff T., et al. Prostate Cancer, Version 2.2019, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw. 2019;17(5):479–505. DOI: 10.6004/jnccn.2019.0023</mixed-citation><mixed-citation xml:lang="en">Mohler J.L., Antonarakis E.S., Armstrong A.J., D’Amico A.V., Davis B.J., Dorff T., et al. Prostate Cancer, Version 2.2019, NCCN Clinical Practice Guidelines in Oncology. J Natl Compr Canc Netw. 2019;17(5):479–505. DOI: 10.6004/jnccn.2019.0023</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Giri V.N., Hegarty S.E., Hyatt C., O’Leary E., Garcia J., Knudsen K.E., et al. Germline genetic testing for inherited prostate cancer in practice: Implications for genetic testing, precision therapy, and cascade testing. Prostate. 2019;79(4):333–9. DOI: 10.1002/pros.23739</mixed-citation><mixed-citation xml:lang="en">Giri V.N., Hegarty S.E., Hyatt C., O’Leary E., Garcia J., Knudsen K.E., et al. Germline genetic testing for inherited prostate cancer in practice: Implications for genetic testing, precision therapy, and cascade testing. Prostate. 2019;79(4):333–9. DOI: 10.1002/pros.23739</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Abida W., Campbell D., Patnaik A. 846PDPreliminary results from the TRITON2 study of rucaparib in patients (pts) with DNA damage repair (DDR)-deficient metastatic castration- resistant prostate cancer (mCRPC): updated analyses. Ann Oncol. 2019;30(5):327–8. DOI: 10.1093/annonc/mdz248.003</mixed-citation><mixed-citation xml:lang="en">Abida W., Campbell D., Patnaik A. 846PDPreliminary results from the TRITON2 study of rucaparib in patients (pts) with DNA damage repair (DDR)-deficient metastatic castration- resistant prostate cancer (mCRPC): updated analyses. Ann Oncol. 2019;30(5):327–8. DOI: 10.1093/annonc/mdz248.003</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Schumacher F.R., Al Olama A.A., Berndt S.I., Benlloch S., Ahmed M., Saunders E., et al. Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. Nat Genet. 2018;50:928–36. DOI: 10.1038/s41588-018-0142-8</mixed-citation><mixed-citation xml:lang="en">Schumacher F.R., Al Olama A.A., Berndt S.I., Benlloch S., Ahmed M., Saunders E., et al. Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci. Nat Genet. 2018;50:928–36. DOI: 10.1038/s41588-018-0142-8</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Hugosson J., Roobol M.J., Månsson M., Tammela T., Zappa M., Nelen V., et al. A 16-yr follow-up of the European Randomized Study of Screening for Prostate Cancer. Eur Urol. 2019;76:43–51. DOI: 10.1016/j.eururo.2019.02.009</mixed-citation><mixed-citation xml:lang="en">Hugosson J., Roobol M.J., Månsson M., Tammela T., Zappa M., Nelen V., et al. A 16-yr follow-up of the European Randomized Study of Screening for Prostate Cancer. Eur Urol. 2019;76:43–51. DOI: 10.1016/j.eururo.2019.02.009</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>
