<?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">tumors</journal-id><journal-title-group><journal-title xml:lang="ru">Malignant tumours</journal-title><trans-title-group xml:lang="en"><trans-title>Malignant tumours</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2224-5057</issn><issn pub-type="epub">2587-6813</issn><publisher><publisher-name>Rosoncoweb</publisher-name></publisher></journal-meta><article-meta><article-id custom-type="elpub" pub-id-type="custom">tumors-551</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>ОРИГИНАЛЬНЫЕ ИССЛЕДОВАНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>ORIGINAL REPORTS</subject></subj-group></article-categories><title-group><article-title>Морфологические особенности BRCA1‑ассоциированных опухолей</article-title><trans-title-group xml:lang="en"><trans-title></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>Иванцов</surname><given-names>А. О.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Насыров</surname><given-names>Р. А.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Имянитов</surname><given-names>E. H.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Соколенко</surname><given-names>А. П.</given-names></name></name-alternatives><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff xml:lang="ru" id="aff-1"><institution>ФГБУ «Научно-исследовательский институт онкологии имени Н. Н. Петрова» Министерства здравоохранения РФ; ФГБОУ ВО «Санкт-Петербургский государственный педиатрический медицинский университет» Министерства здравоохранения РФ.</institution><country>Russian Federation</country></aff><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>12</day><month>11</month><year>2018</year></pub-date><volume>8</volume><issue>3s1</issue><fpage>90</fpage><lpage>95</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Иванцов А.О., Насыров Р.А., Имянитов E.H., Соколенко А.П., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Иванцов А.О., Насыров Р.А., Имянитов E.H., Соколенко А.П.</copyright-holder><copyright-holder xml:lang="en">Иванцов А.О., Насыров Р.А., Имянитов E.H., Соколенко А.П.</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.malignanttumors.org/jour/article/view/551">https://www.malignanttumors.org/jour/article/view/551</self-uri><abstract><p>BRCA1‑ассоциированные новообразования представляют собой большую гетерогенную группу опухолей с различным фенотипом, клинической картиной и прогнозом. Наличие мутации BRCA1 позволяет использовать современные эффективные стратегии лекарственной терапии опухолей с использованием PARP-ингибиторов для достижения наилучших результатов лечения. Новообразования молочной железы и яичника у носителей мутаций BRCA1 возникают значительно чаще, чем опухоли иных локализаций. BRCA1‑ассоциированные карциномы имеют определенные морфологические особенности, которые позволяют рекомендовать пациентам проведение молекулярно-генетического исследования.</p></abstract><kwd-group xml:lang="ru"><kwd>BRCA1</kwd><kwd>мутация</kwd><kwd>рак</kwd><kwd>морфологические особенности</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">Armes J., Egan A., Southey M., et al. The histologic phenotypes of breast carcinoma occurring before age 40 years in women with and without BRCA1 or BRCA2 germline mutations: a population-based study // Cancer. 1998. Vol. 83(11). p. 2335–45.</mixed-citation><mixed-citation xml:lang="en">Armes J., Egan A., Southey M., et al. The histologic phenotypes of breast carcinoma occurring before age 40 years in women with and without BRCA1 or BRCA2 germline mutations: a population-based study // Cancer. 1998. Vol. 83(11). p. 2335–45.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Atchley D., Albarracin C., Lopez A., et al. Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer // J Clin Oncol. 2008. Vol. 26. p. 4282–8.</mixed-citation><mixed-citation xml:lang="en">Atchley D., Albarracin C., Lopez A., et al. Clinical and pathologic characteristics of patients with BRCA-positive and BRCA-negative breast cancer // J Clin Oncol. 2008. Vol. 26. p. 4282–8.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Biron-Shental T, Drucker L, Altaras M, et al. High incidence of BRCA1-2 germline mutations, previous breast cancer and familial cancer history in Jewish patients with uterine serous papillary carcinoma // Eur J Surg Oncol. 2006. 32(10). p. 1097–100.</mixed-citation><mixed-citation xml:lang="en">Biron-Shental T, Drucker L, Altaras M, et al. High incidence of BRCA1-2 germline mutations, previous breast cancer and familial cancer history in Jewish patients with uterine serous papillary carcinoma // Eur J Surg Oncol. 2006. 32(10). p. 1097–100.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Breast Cancer Linkage Consortium Pathology of familial breast cancer: differences between breast cancer in carriers of BRCA1 or BRCA2 mutations and sporadic cases // Lancet. 1997. Vol. 349. p. 1505–1510.</mixed-citation><mixed-citation xml:lang="en">Breast Cancer Linkage Consortium Pathology of familial breast cancer: differences between breast cancer in carriers of BRCA1 or BRCA2 mutations and sporadic cases // Lancet. 1997. Vol. 349. p. 1505–1510.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Bruchim I, Amichay K, Kidron D, et al. BRCA1/2 germline mutations in Jewish patients with uterine serous carcinoma // Int J Gynecol Cancer. 2010. 20(7). p. 1148–53.</mixed-citation><mixed-citation xml:lang="en">Bruchim I, Amichay K, Kidron D, et al. BRCA1/2 germline mutations in Jewish patients with uterine serous carcinoma // Int J Gynecol Cancer. 2010. 20(7). p. 1148–53.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Castro E., Goh C., Olmos D., et al. Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer // J Clin Oncol. 2013. Vol. 31(14). p. 1748–57.</mixed-citation><mixed-citation xml:lang="en">Castro E., Goh C., Olmos D., et al. Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer // J Clin Oncol. 2013. Vol. 31(14). p. 1748–57.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Crook T., Crossland S., Crompton M., et al. p53 mutations in BRCA1-associated familial breast cancer // Lancet. 1997. Vol. 350(9078). p. 638–9.</mixed-citation><mixed-citation xml:lang="en">Crook T., Crossland S., Crompton M., et al. p53 mutations in BRCA1-associated familial breast cancer // Lancet. 1997. Vol. 350(9078). p. 638–9.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Coleman, M.P., Forman D., Bryant H. et al. Cancer survival in Australia, Canada, Denmark, Norway, Sweden and the UK, 1995–2007 (the International Cancer Benchmarking 154 Partnership): an analysis of population-based cancer registry data // Lancet. 2011. 377(9760). P. 127–138.</mixed-citation><mixed-citation xml:lang="en">Coleman, M.P., Forman D., Bryant H. et al. Cancer survival in Australia, Canada, Denmark, Norway, Sweden and the UK, 1995–2007 (the International Cancer Benchmarking 154 Partnership): an analysis of population-based cancer registry data // Lancet. 2011. 377(9760). P. 127–138.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Eisinger F., Stoppa-Lyonnet D., Longy M., et al. Germ line mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancer // Cancer Res. 1996. Vol. 56. p. 471–474.</mixed-citation><mixed-citation xml:lang="en">Eisinger F., Stoppa-Lyonnet D., Longy M., et al. Germ line mutation at BRCA1 affects the histoprognostic grade in hereditary breast cancer // Cancer Res. 1996. Vol. 56. p. 471–474.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Eisinger F., Jacquemier J., Charpin C., et al. Mutations at BRCA1: the medullary breast carcinoma revisited // Cancer Res. 1998. Vol. 58(8). p. 1588–92.</mixed-citation><mixed-citation xml:lang="en">Eisinger F., Jacquemier J., Charpin C., et al. Mutations at BRCA1: the medullary breast carcinoma revisited // Cancer Res. 1998. Vol. 58(8). p. 1588–92.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Evans D., Lalloo F., Howell S., et al. Low prevalence of HER2 positivity amongst BRCA1 and BRCA2 mutation carriers and in primary BRCA screens // Breast Cancer Res Treat. 2016. Vol. 155(3). p. 597–601.</mixed-citation><mixed-citation xml:lang="en">Evans D., Lalloo F., Howell S., et al. Low prevalence of HER2 positivity amongst BRCA1 and BRCA2 mutation carriers and in primary BRCA screens // Breast Cancer Res Treat. 2016. Vol. 155(3). p. 597–601.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Evans T., Sany O., Pearmain P. et al. Differential trends in the rising incidence of endometrial cancer by type: data from a UK population-based registry from 1994 to 2006 // British Journal of Cancer. 2011. Vol. 104. № 9. Р. 1505–1510.</mixed-citation><mixed-citation xml:lang="en">Evans T., Sany O., Pearmain P. et al. Differential trends in the rising incidence of endometrial cancer by type: data from a UK population-based registry from 1994 to 2006 // British Journal of Cancer. 2011. Vol. 104. № 9. Р. 1505–1510.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Ferlay J., Soerjomataram I., Ervik M., et al. et al. GLOBOCAN 2012 v. 1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11 [Internet].</mixed-citation><mixed-citation xml:lang="en">Ferlay J., Soerjomataram I., Ervik M., et al. et al. GLOBOCAN 2012 v. 1.0, Cancer Incidence and Mortality Worldwide: IARC CancerBase No. 11 [Internet].</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Ferrone C., Levine D., Tang L. et al. BRCA germline mutations in Jewish patients with pancreatic adenocarcinoma // J. Clin. Oncol. 2009. Vol. 27 p. 433–438.</mixed-citation><mixed-citation xml:lang="en">Ferrone C., Levine D., Tang L. et al. BRCA germline mutations in Jewish patients with pancreatic adenocarcinoma // J. Clin. Oncol. 2009. Vol. 27 p. 433–438.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Foulkes W., Metcalfe K., Sun P., et al. Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: the influence of age, grade, and histological type // Clin Cancer Res. 2004. Vol. 10. p. 2029–34.</mixed-citation><mixed-citation xml:lang="en">Foulkes W., Metcalfe K., Sun P., et al. Estrogen receptor status in BRCA1- and BRCA2-related breast cancer: the influence of age, grade, and histological type // Clin Cancer Res. 2004. Vol. 10. p. 2029–34.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Gallagher D., Gaudet M., Pal P., et al. Germline BRCA mutations denote a clinicopathologic subset of prostate cancer // Clin Cancer Res. 2010. Vol. 16(7). p. 2115–21.</mixed-citation><mixed-citation xml:lang="en">Gallagher D., Gaudet M., Pal P., et al. Germline BRCA mutations denote a clinicopathologic subset of prostate cancer // Clin Cancer Res. 2010. Vol. 16(7). p. 2115–21.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Giusti R., Rutter J., Duray P., et al. A twofold increase in BRCA mutation related prostate cancer among Ashkenazi Israelis is not associated with distinctive histopathology // J Med Genet. 2003. Vol. 40(10). p. 787–92.</mixed-citation><mixed-citation xml:lang="en">Giusti R., Rutter J., Duray P., et al. A twofold increase in BRCA mutation related prostate cancer among Ashkenazi Israelis is not associated with distinctive histopathology // J Med Genet. 2003. Vol. 40(10). p. 787–92.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Jaworowska E., Tarnowska C., Lubinski J., et al. Clinical characteristics of laryngeal cancer in BRCA-1 mutation carriers. Anticancer Res. 2009. Vol. 29(7). p. 2703–5.</mixed-citation><mixed-citation xml:lang="en">Jaworowska E., Tarnowska C., Lubinski J., et al. Clinical characteristics of laryngeal cancer in BRCA-1 mutation carriers. Anticancer Res. 2009. Vol. 29(7). p. 2703–5.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Johannsson O., Idvall I., Anderson C., et al. Tumour biological features of BRCA1-induced breast and ovarian cancer // Eur J Cancer. 1997. Vol. 33(3). p. 362–71.</mixed-citation><mixed-citation xml:lang="en">Johannsson O., Idvall I., Anderson C., et al. Tumour biological features of BRCA1-induced breast and ovarian cancer // Eur J Cancer. 1997. Vol. 33(3). p. 362–71.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Haffty B., Choi D., Goyal S., et al. Breast cancer in young women (YBC): prevalence of BRCA1/2 mutations and risk of secondary malignancies across diverse racial groups // Ann Oncol. 2009. Vol. 20(10). p. 1653–9.</mixed-citation><mixed-citation xml:lang="en">Haffty B., Choi D., Goyal S., et al. Breast cancer in young women (YBC): prevalence of BRCA1/2 mutations and risk of secondary malignancies across diverse racial groups // Ann Oncol. 2009. Vol. 20(10). p. 1653–9.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Hassanein M., Huiart L., Bourdon V., et al. Prediction of BRCA1 germ-line mutation status in patients with breast cancer using histoprognosis grade, MS110, Lys27H3, vimentin, and KI67 // Pathobiology. 2013. Vol. 80(5). p. 219–27.</mixed-citation><mixed-citation xml:lang="en">Hassanein M., Huiart L., Bourdon V., et al. Prediction of BRCA1 germ-line mutation status in patients with breast cancer using histoprognosis grade, MS110, Lys27H3, vimentin, and KI67 // Pathobiology. 2013. Vol. 80(5). p. 219–27.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Heerma van Voss M., van der Groep P., Bart J., et al. Lympho-vascular invasion in BRCA related breast cancer compared to sporadic controls // BMC Cancer. 2010. Vol 16. p. 145.</mixed-citation><mixed-citation xml:lang="en">Heerma van Voss M., van der Groep P., Bart J., et al. Lympho-vascular invasion in BRCA related breast cancer compared to sporadic controls // BMC Cancer. 2010. Vol 16. p. 145.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Holter S., Borgida A., Dodd A., et al. Germline BRCA Mutations in a Large Clinic-Based Cohort of Patients With Pancreatic Adenocarcinoma // J Clin Oncol. 2015. Vol. 33(28). p. 3124–9.</mixed-citation><mixed-citation xml:lang="en">Holter S., Borgida A., Dodd A., et al. Germline BRCA Mutations in a Large Clinic-Based Cohort of Patients With Pancreatic Adenocarcinoma // J Clin Oncol. 2015. Vol. 33(28). p. 3124–9.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Hussein Y., Ducie J., Arnold A., et al. Invasion Patterns of Metastatic Extrauterine High-grade Serous Carcinoma With BRCA Germline Mutation and Correlation With Clinical Outcomes // Am J Surg Pathol. 2016. Vol. 40(3). p. 404–9.</mixed-citation><mixed-citation xml:lang="en">Hussein Y., Ducie J., Arnold A., et al. Invasion Patterns of Metastatic Extrauterine High-grade Serous Carcinoma With BRCA Germline Mutation and Correlation With Clinical Outcomes // Am J Surg Pathol. 2016. Vol. 40(3). p. 404–9.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Konstantinopoulos P., Spentzos D., Karlan B., et al. Gene expression profile of BRCAness that correlates with responsiveness to chemotherapy and with outcome in patients with epithelial ovarian cancer // J Clin Oncol. 2010. Vol. 28(22). p. 3555-61.</mixed-citation><mixed-citation xml:lang="en">Konstantinopoulos P., Spentzos D., Karlan B., et al. Gene expression profile of BRCAness that correlates with responsiveness to chemotherapy and with outcome in patients with epithelial ovarian cancer // J Clin Oncol. 2010. Vol. 28(22). p. 3555-61.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Kuligina E., Reiner A., Imyanitov E., Begg C. Evaluating cancer epidemiologic risk factors using multiple primary malignancies // Epidemiology. 2010. Vol. 21(3). p. 366–372.</mixed-citation><mixed-citation xml:lang="en">Kuligina E., Reiner A., Imyanitov E., Begg C. Evaluating cancer epidemiologic risk factors using multiple primary malignancies // Epidemiology. 2010. Vol. 21(3). p. 366–372.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Lal G., Liu G., Schmocker B. et al. Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations // Cancer Res. 2000. Vol. 60. p. 409–416.</mixed-citation><mixed-citation xml:lang="en">Lal G., Liu G., Schmocker B. et al. Inherited predisposition to pancreatic adenocarcinoma: role of family history and germ-line p16, BRCA1, and BRCA2 mutations // Cancer Res. 2000. Vol. 60. p. 409–416.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Lakhani S., Jacquemier J., Sloane J., et al. Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations // J Natl Cancer Inst.1998. Vol. 90(15). p. 1138–45.</mixed-citation><mixed-citation xml:lang="en">Lakhani S., Jacquemier J., Sloane J., et al. Multifactorial analysis of differences between sporadic breast cancers and cancers involving BRCA1 and BRCA2 mutations // J Natl Cancer Inst.1998. Vol. 90(15). p. 1138–45.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Lakhani S., Van De Vijver M., Jacquemier J., et al. The pathology of familial breast cancer: predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2 // J Clin Oncol. 2002. Vol. 20. p. 2310–8.</mixed-citation><mixed-citation xml:lang="en">Lakhani S., Van De Vijver M., Jacquemier J., et al. The pathology of familial breast cancer: predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2 // J Clin Oncol. 2002. Vol. 20. p. 2310–8.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Lakhani S., Reis-Filho J., Fulford L., et al. Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype // Clin Cancer Res. 2005. Vol. 11. p. 5175–80.</mixed-citation><mixed-citation xml:lang="en">Lakhani S., Reis-Filho J., Fulford L., et al. Prediction of BRCA1 status in patients with breast cancer using estrogen receptor and basal phenotype // Clin Cancer Res. 2005. Vol. 11. p. 5175–80.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Lavie O., Ben-Arie A, Segev Y, et al. BRCA germline mutations in women with uterine serous carcinoma--still a debate // Int J Gynecol Cancer. 2010. Vol. 20(9). p. 1531–4.</mixed-citation><mixed-citation xml:lang="en">Lavie O., Ben-Arie A, Segev Y, et al. BRCA germline mutations in women with uterine serous carcinoma--still a debate // Int J Gynecol Cancer. 2010. Vol. 20(9). p. 1531–4.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Lawniczak M., Gawin A., Biafek A. et al. Is there any relationship between BRCA1 gene mutation and pancreatic cancer development? // Pol. Arch. Med. Wewn. 2008. Vol. 118. p. 645–649.</mixed-citation><mixed-citation xml:lang="en">Lawniczak M., Gawin A., Biafek A. et al. Is there any relationship between BRCA1 gene mutation and pancreatic cancer development? // Pol. Arch. Med. Wewn. 2008. Vol. 118. p. 645–649.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Levine D., Lin O., Barakat R., et al. Risk of endometrial carcinoma associated with BRCA mutation // Gynecol Oncol. 2001. Vol. 80(3). p. 395–8.</mixed-citation><mixed-citation xml:lang="en">Levine D., Lin O., Barakat R., et al. Risk of endometrial carcinoma associated with BRCA mutation // Gynecol Oncol. 2001. Vol. 80(3). p. 395–8.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Lucas A., Shakya R., Lipsyc M., et al. High prevalence of BRCA1 and BRCA2 germline mutations with loss of heterozygosity in a series of resected pancreatic adenocarcinoma and other neoplastic lesions // Clin Cancer Res. 2013. Vol. 19. p. 3396–3403.</mixed-citation><mixed-citation xml:lang="en">Lucas A., Shakya R., Lipsyc M., et al. High prevalence of BRCA1 and BRCA2 germline mutations with loss of heterozygosity in a series of resected pancreatic adenocarcinoma and other neoplastic lesions // Clin Cancer Res. 2013. Vol. 19. p. 3396–3403.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Mangia A., Tommasi S., Bruno M., et al. Histological features of extratumoral breast lesions as a predictive factor of familial breast cancer // Oncol Rep. 2010. Vol. 23(6). p. 1641–5.</mixed-citation><mixed-citation xml:lang="en">Mangia A., Tommasi S., Bruno M., et al. Histological features of extratumoral breast lesions as a predictive factor of familial breast cancer // Oncol Rep. 2010. Vol. 23(6). p. 1641–5.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Mavaddat N., Barrowdale D., Andrulis I., et al. Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) // Cancer Epidemiol Biomarkers Prev. 2012. Vol. 21(1). p. 134-47.</mixed-citation><mixed-citation xml:lang="en">Mavaddat N., Barrowdale D., Andrulis I., et al. Pathology of breast and ovarian cancers among BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA) // Cancer Epidemiol Biomarkers Prev. 2012. Vol. 21(1). p. 134-47.</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Mitra A., Jameson C., Barbachano Y. et al. Elevated expression of Ki-67 identifies aggressive prostate cancers but does not distinguish BRCA1 or BRCA2 mutation carriers // Oncol Rep. 2010. Vol. 23(2). p. 299–305.</mixed-citation><mixed-citation xml:lang="en">Mitra A., Jameson C., Barbachano Y. et al. Elevated expression of Ki-67 identifies aggressive prostate cancers but does not distinguish BRCA1 or BRCA2 mutation carriers // Oncol Rep. 2010. Vol. 23(2). p. 299–305.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Mohanty S., Lai J., Gordon O., et al. BRCA-mutated Invasive Breast Carcinomas: Immunohistochemical Analysis of Insulin-like Growth Factor II mRNA-binding Protein (IMP3), Cytokeratin 8/18, and Cytokeratin 14 // Breast J. 2015. Vol. 21(6). p. 596–603.</mixed-citation><mixed-citation xml:lang="en">Mohanty S., Lai J., Gordon O., et al. BRCA-mutated Invasive Breast Carcinomas: Immunohistochemical Analysis of Insulin-like Growth Factor II mRNA-binding Protein (IMP3), Cytokeratin 8/18, and Cytokeratin 14 // Breast J. 2015. Vol. 21(6). p. 596–603.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Moiseyenko V., Volkov N., Suspistin E., et al. Evidence for predictive role of BRCA1 and bTUBIII in gastric cancer // Med Oncol. 2013. Vol. 30(2). p. 545.</mixed-citation><mixed-citation xml:lang="en">Moiseyenko V., Volkov N., Suspistin E., et al. Evidence for predictive role of BRCA1 and bTUBIII in gastric cancer // Med Oncol. 2013. Vol. 30(2). p. 545.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Noh J., Choi D., Baek H., et al. Associations between BRCA Mutations in High-Risk Breast Cancer Patients and Familial Cancers Other than Breast or Ovary // J Breast Cancer. 2012. Vol. 15(3). p. 283–7.</mixed-citation><mixed-citation xml:lang="en">Noh J., Choi D., Baek H., et al. Associations between BRCA Mutations in High-Risk Breast Cancer Patients and Familial Cancers Other than Breast or Ovary // J Breast Cancer. 2012. Vol. 15(3). p. 283–7.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Noori S., Gangi A., Nelson M., et al. Comparison of nodal metastasis between BRCA mutation carriers and non-BRCA mutation carriers with breast cancer // Ann Surg Oncol. 2014. Vol. 21(10). p. 3324–9.</mixed-citation><mixed-citation xml:lang="en">Noori S., Gangi A., Nelson M., et al. Comparison of nodal metastasis between BRCA mutation carriers and non-BRCA mutation carriers with breast cancer // Ann Surg Oncol. 2014. Vol. 21(10). p. 3324–9.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">Palacios J., Honrado E., Osorio A., et al. Phenotypic characterization of BRCA1 and BRCA2 tumors based in a tissue microarray study with 37 immunohistochemical markers // Breast Cancer Res Treat. 2005. Vol. 90:5. p. 14.</mixed-citation><mixed-citation xml:lang="en">Palacios J., Honrado E., Osorio A., et al. Phenotypic characterization of BRCA1 and BRCA2 tumors based in a tissue microarray study with 37 immunohistochemical markers // Breast Cancer Res Treat. 2005. Vol. 90:5. p. 14.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Pierce L., Phillips K., Griffith K., et al. Local therapy in BRCA1 and BRCA2 mutation carriers with operable breast cancer: comparison of breast conservation and mastectomy // Breast Cancer Res Treat. 2010. Vol. 121(2). p. 389–98.</mixed-citation><mixed-citation xml:lang="en">Pierce L., Phillips K., Griffith K., et al. Local therapy in BRCA1 and BRCA2 mutation carriers with operable breast cancer: comparison of breast conservation and mastectomy // Breast Cancer Res Treat. 2010. Vol. 121(2). p. 389–98.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Pennington KP, Walsh T, Lee M, et al. BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma // Cancer. 2013. Vol. 119(2). p. 332–8.</mixed-citation><mixed-citation xml:lang="en">Pennington KP, Walsh T, Lee M, et al. BRCA1, TP53, and CHEK2 germline mutations in uterine serous carcinoma // Cancer. 2013. Vol. 119(2). p. 332–8.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Plakhins G., Irmejs A., Gardovskis A., et al. Genotype-phenotype correlations among BRCA1 4153delA and 5382insC mutation carriers from Latvia // BMC Med Genet. 2011. Vol. 12. p. 147.</mixed-citation><mixed-citation xml:lang="en">Plakhins G., Irmejs A., Gardovskis A., et al. Genotype-phenotype correlations among BRCA1 4153delA and 5382insC mutation carriers from Latvia // BMC Med Genet. 2011. Vol. 12. p. 147.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Reyes M., Arnold A., Kauff N., et al. Invasion patterns of metastatic high-grade serous carcinoma of ovary or fallopian tube associated with BRCA deficiency // Mod Pathol. 2014. Vol. 27(10). p. 1405–11.</mixed-citation><mixed-citation xml:lang="en">Reyes M., Arnold A., Kauff N., et al. Invasion patterns of metastatic high-grade serous carcinoma of ovary or fallopian tube associated with BRCA deficiency // Mod Pathol. 2014. Vol. 27(10). p. 1405–11.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Ricci S., Shafer A., Nerenstone S., et al. A surveillance conundrum: a case of 4 distinct primary malignancies in a BRCA-1 mutation carrier // Int J Gynecol Pathol. 2012. Vol. 31(2). p. 145–8.</mixed-citation><mixed-citation xml:lang="en">Ricci S., Shafer A., Nerenstone S., et al. A surveillance conundrum: a case of 4 distinct primary malignancies in a BRCA-1 mutation carrier // Int J Gynecol Pathol. 2012. Vol. 31(2). p. 145–8.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Schlichtholz B., Bouchind’homme B., Pages S., et al. p53 mutations in BRCA1-associated familial breast cancer // Lancet. 1998. Vol. 352(9128). p. 622.</mixed-citation><mixed-citation xml:lang="en">Schlichtholz B., Bouchind’homme B., Pages S., et al. p53 mutations in BRCA1-associated familial breast cancer // Lancet. 1998. Vol. 352(9128). p. 622.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Segev Y., Iqbal J., Lubinski J., et al. The incidence of endometrial cancer in women with BRCA1 and BRCA2 mutations: an international prospective cohort study // Gynecol Oncol. 2013. Vol.130(1). p. 127–31.</mixed-citation><mixed-citation xml:lang="en">Segev Y., Iqbal J., Lubinski J., et al. The incidence of endometrial cancer in women with BRCA1 and BRCA2 mutations: an international prospective cohort study // Gynecol Oncol. 2013. Vol.130(1). p. 127–31.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Shen T., Teknos T., Toland A., et al. Salivary gland cancer in BRCA-positive families: a retrospective review // JAMA Otolaryngol Head Neck Surg. 2014. Vol. 140(12). p. 1213–7.</mixed-citation><mixed-citation xml:lang="en">Shen T., Teknos T., Toland A., et al. Salivary gland cancer in BRCA-positive families: a retrospective review // JAMA Otolaryngol Head Neck Surg. 2014. Vol. 140(12). p. 1213–7.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Singer C., Zabkova P., Rappaport C., et al. Presence of intratumoral stem cells in breast cancer patients with or without BRCA germline mutations // Curr Cancer Drug Targets. 2012. Vol. 12(1). p. 44–50.</mixed-citation><mixed-citation xml:lang="en">Singer C., Zabkova P., Rappaport C., et al. Presence of intratumoral stem cells in breast cancer patients with or without BRCA germline mutations // Curr Cancer Drug Targets. 2012. Vol. 12(1). p. 44–50.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Sorlie T., Tibshirani R., Parker J., et al. Repeated observation of breast tumor subtypes in independent gene expression data sets // Proc Natl Acad Sci U S A. 2003. Vol. 100. p. 8418–23.</mixed-citation><mixed-citation xml:lang="en">Sorlie T., Tibshirani R., Parker J., et al. Repeated observation of breast tumor subtypes in independent gene expression data sets // Proc Natl Acad Sci U S A. 2003. Vol. 100. p. 8418–23.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Southey M.C, Ramus S., Dowty J., et al. Morphological predictors of BRCA1 germline mutations in young women with breast cancer // Br J Cancer. 2011. Vol. 104(6). p. 903–9.</mixed-citation><mixed-citation xml:lang="en">Southey M.C, Ramus S., Dowty J., et al. Morphological predictors of BRCA1 germline mutations in young women with breast cancer // Br J Cancer. 2011. Vol. 104(6). p. 903–9.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Soslow R., Han G., Park K., et al. Morphologic patterns associated with BRCA1 and BRCA2 genotype in ovarian carcinoma // Mod Pathol. 2012. Vol. 25(4). p. 625–36.</mixed-citation><mixed-citation xml:lang="en">Soslow R., Han G., Park K., et al. Morphologic patterns associated with BRCA1 and BRCA2 genotype in ovarian carcinoma // Mod Pathol. 2012. Vol. 25(4). p. 625–36.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Suspitsin E., Sherina N., Ponomariova D., et al. High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients // Hered Cancer Clin Pract. 2009. Vol. 7(1). p. 5.</mixed-citation><mixed-citation xml:lang="en">Suspitsin E., Sherina N., Ponomariova D., et al. High frequency of BRCA1, but not CHEK2 or NBS1 (NBN), founder mutations in Russian ovarian cancer patients // Hered Cancer Clin Pract. 2009. Vol. 7(1). p. 5.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Thompson K., Hernandez J., Canby-Hagino E., et al. Prognostic features in men who died of prostate cancer // J Urol. 2005. Vol. 174. p. 553–6.</mixed-citation><mixed-citation xml:lang="en">Thompson K., Hernandez J., Canby-Hagino E., et al. Prognostic features in men who died of prostate cancer // J Urol. 2005. Vol. 174. p. 553–6.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Tucker H., Charles Z., Robertson J., Adam J. NICE guidance on olaparib for maintenance treatment of patients with relapsed, platinum-sensitive, BRCA mutation-positive ovarian cancer // Lancet Oncol. 2016. Vol. 17(3). p. 277–8.</mixed-citation><mixed-citation xml:lang="en">Tucker H., Charles Z., Robertson J., Adam J. NICE guidance on olaparib for maintenance treatment of patients with relapsed, platinum-sensitive, BRCA mutation-positive ovarian cancer // Lancet Oncol. 2016. Vol. 17(3). p. 277–8.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Vargas A., Da Silva L., Lakhani S. The contribution of breast cancer pathology to statistical models to predict mutation risk in BRCA carriers // Fam Cancer. 2010. Vol. 9(4). p. 545–53.</mixed-citation><mixed-citation xml:lang="en">Vargas A., Da Silva L., Lakhani S. The contribution of breast cancer pathology to statistical models to predict mutation risk in BRCA carriers // Fam Cancer. 2010. Vol. 9(4). p. 545–53.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Waisbren J., Uthe R., Siziopikou K., Kaklamani V. BRCA 1/2 gene mutation and gastrointestinal stromal tumours: a potential association // BMJ Case Rep. 2015. pii: bcr2014208830.</mixed-citation><mixed-citation xml:lang="en">Waisbren J., Uthe R., Siziopikou K., Kaklamani V. BRCA 1/2 gene mutation and gastrointestinal stromal tumours: a potential association // BMJ Case Rep. 2015. pii: bcr2014208830.</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>
