<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Surgery and Oncology</journal-id><journal-title-group><journal-title xml:lang="en">Surgery and Oncology</journal-title><trans-title-group xml:lang="ru"><trans-title>Хирургия и онкология</trans-title></trans-title-group></journal-title-group><issn publication-format="electronic">2949-5857</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">552</article-id><article-id pub-id-type="doi">10.17650/2686-9594-2022-12-3-43-50</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>LITERATURE REVIEW</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject>Unknown</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Endoscopic criteria and promising biomarkers for serrated adenomas of the colon (literature review)</article-title><trans-title-group xml:lang="ru"><trans-title>Эндоскопические критерии и перспективные биомаркеры зубчатых аденом ободочной кишки (обзор литературы)</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-7025-970X</contrib-id><name-alternatives><name xml:lang="en"><surname>Karasev</surname><given-names>I. A.</given-names></name><name xml:lang="ru"><surname>Карасев</surname><given-names>И. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>Ivan Aleksandrovich Karasev</p>
<p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>Иван Александрович Карасев</p>
<p>115478 Москва, Каширское шоссе, 24</p></bio><email>ronc-karasev@yandex.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Stroganova</surname><given-names>A. M.</given-names></name><name xml:lang="ru"><surname>Строганова</surname><given-names>А. М.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><email>info@abvpress.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Malikhova</surname><given-names>O. A.</given-names></name><name xml:lang="ru"><surname>Малихова</surname><given-names>О. А.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><email>info@abvpress.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1787-1019</contrib-id><name-alternatives><name xml:lang="en"><surname>Davydkina</surname><given-names>T. S.</given-names></name><name xml:lang="ru"><surname>Давыдкина</surname><given-names>Т. С.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><email>info@abvpress.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4294-1995</contrib-id><name-alternatives><name xml:lang="en"><surname>Grigoryevskaya</surname><given-names>Z. V.</given-names></name><name xml:lang="ru"><surname>Григорьевская</surname><given-names>З. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><email>info@abvpress.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Tereshchenko</surname><given-names>I. V.</given-names></name><name xml:lang="ru"><surname>Терещенко</surname><given-names>И. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><email>info@abvpress.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Pospekhova</surname><given-names>N. I.</given-names></name><name xml:lang="ru"><surname>Поспехова</surname><given-names>Н. И.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><email>info@abvpress.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8783-8874</contrib-id><name-alternatives><name xml:lang="en"><surname>Semyanikhina</surname><given-names>A. V.</given-names></name><name xml:lang="ru"><surname>Семьянихина</surname><given-names>А. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><bio xml:lang="en"><p>24 Kashirskoe Shosse, Moscow 115478</p></bio><bio xml:lang="ru"><p>115478 Москва, Каширское шоссе, 24</p></bio><email>info@abvpress.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N. N. Blokhin Russian Cancer Research Center, Ministry of Health of Russia</institution></aff><aff><institution xml:lang="ru">ФГБУ «Национальный медицинский исследовательский центр онкологии им. Н. Н. Блохина» Минздрава России</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2022-09-07" publication-format="electronic"><day>07</day><month>09</month><year>2022</year></pub-date><volume>12</volume><issue>3</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>43</fpage><lpage>50</lpage><history><date date-type="received" iso-8601-date="2022-09-07"><day>07</day><month>09</month><year>2022</year></date><date date-type="accepted" iso-8601-date="2022-09-07"><day>07</day><month>09</month><year>2022</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2022, Karasev I.A., Stroganova A.M., Malikhova O.A., Davydkina T.S., Grigoryevskaya Z.V., Tereshchenko I.V., Pospekhova N.I., Semyanikhina A.V.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2022, Карасев И.А., Строганова А.М., Малихова О.А., Давыдкина Т.С., Григорьевская З.В., Терещенко И.В., Поспехова Н.И., Семьянихина А.В.</copyright-statement><copyright-year>2022</copyright-year><copyright-holder xml:lang="en">Karasev I.A., Stroganova A.M., Malikhova O.A., Davydkina T.S., Grigoryevskaya Z.V., Tereshchenko I.V., Pospekhova N.I., Semyanikhina A.V.</copyright-holder><copyright-holder xml:lang="ru">Карасев И.А., Строганова А.М., Малихова О.А., Давыдкина Т.С., Григорьевская З.В., Терещенко И.В., Поспехова Н.И., Семьянихина А.В.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://onco-surgery.info/jour/article/view/552">https://onco-surgery.info/jour/article/view/552</self-uri><abstract xml:lang="en"><p>Colorectal cancer (CRC) is one of the leading causes of death from cancer in many countries of the world, both in men and women, and these rates are on the rise. The probability of suffering from CRC is about 4–5 % and the risk for developing CRC is associated with personal features or habits such as age, chronic disease history and lifestyle, but in most cases colorectal cancer develops as a result of the degeneration of adenomatous formations or along the jagged path. Immune dysregulation, dysbiosis, and epithelial destruction contribute to colorectal cancer carcinogenesis. The gut microbiota has a relevant role, and dysbiosis situations can induce colonic carcinogenesis through a chronic inflammation mechanism. Some of the bacteria responsible for this multiphase process include <italic>Fusobacterium</italic> spp., <italic>Bacteroides fragilis</italic> and enteropathogenic <italic>Escherichia coli</italic>. moreover, CRC is caused by mutations that target oncogenes, tumour suppressor genes and genes related to DNA repair mechanisms.</p> <p>Considering that the average time for the development of adenocarcinoma from precancer takes about 10 years, changes in the microbiota can be a prospective marker for screening precancerous conditions of the colon, as well as the detection of changes in DNA.</p> <p>The work will discuss the relationship between changes in the microbial composition of the colon with the genetic mutations identified by molecular genetic sequencing.</p></abstract><trans-abstract xml:lang="ru"><p>Колоректальный рак (КРР) является одной из ведущих причин смертности от онкологических заболеваний во многих странах мира, как у мужчин, так и у женщин, и эти показатели имеют тенденцию к росту. Вероятность развития КРР составляет около 4–5 %, риск его развития связан с индивидуальными особенностями организма, вредными привычками, возрастом, хроническими заболеваниями и образом жизни, однако в большинстве случаев КРР развивается вследствие перерождения аденоматозных образований или по пути метаплазии из зубчатых аденом, его канцерогенезу содействуют иммунная дисрегуляция, дисбиоз и разрушение эпителия. Микробиота кишечника играет важную роль в канцерогенезе, вероятно, через механизм хронического воспаления. Некоторые из бактерий, ответственных за этот многофазный процесс, включают <italic>Fusobacterium</italic> spp., <italic>Bacteroides</italic><italic> </italic><italic>fragilis</italic> и энтеропатогенные <italic>Escherichia</italic><italic> </italic><italic>coli</italic>. кроме того, КРР вызывается мутациями, нацеленными на онкогены, гены – супрессоры опухолей и гены, связанные с механизмами репарации ДНК.</p> <p>С учетом того, что среднее время развития аденокарциномы из предрака занимает около 10 лет, изменение кишечной микрофлоры может являться перспективным маркером для скрининга предраковых состояний толстой кишки, как и обнаружение изменений в ДНК.</p> <p>В работе пойдет речь о взаимосвязи изменений микробного состава толстой кишки с выявленными путем молекулярно-генетического секвенирования генными мутациями.</p></trans-abstract><kwd-group xml:lang="en"><kwd>colorectal cancer</kwd><kwd>microbiota</kwd><kwd>molecular genetic research</kwd><kwd>serrated adenoma</kwd><kwd>biomarkers</kwd><kwd>endoscopy</kwd><kwd>screening</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>колоректальный рак</kwd><kwd>микробиота</kwd><kwd>молекулярно-генетическое исследование</kwd><kwd>зубчатая аденома</kwd><kwd>биомаркеры</kwd><kwd>эндоскопия</kwd><kwd>скрининг</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Bray F., Ferlay J., Soerjomataram I. et al. Global Cancer Statistics 2018: GLOBOCAN Estimates of Incidence and Mortality Worldwide for 36 Cancers in 185 Countries. CA Cancer J Clin 2018;68(6):394–424. DOI: 10.3322/caac.21492</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Jass J.R. Classification of colorectal cancer based on correlation of clinical, morphological and molecular features. Histopathology 2007;50:113–30. DOI: 10.1111/j.1365-2559.2006.02549.x</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Ng S.C., Ching J.Y., Chan V.C. et al. Association between serrated polyps and the risk of synchronous advanced colorectal neoplasia in average-risk individuals. Aliment Pharmacol Ther 2015;41:108–15. DOI: 10.1111/apt.13003</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Jass J.R. Large intestine. Histological typing of intestinal tumours. In: World Health Organization international histological classification of tumours, 2nd edn. Berlin: Springer-Verlag, 1989. P. 30.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Leggett B.A., Devereaux B., Biden K. et al. Hyperplastic polyposis: association with colorectal cancer. Am J Surg Pathol 2001;25:177–84.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Patil D.T., Shadrach B.L., Rybicki L.A. et al. Proximal colon cancers and the serrated pathway: a systematic analysis of precursor histology and BRAF mutation status. Mod Pathol 2012;25: 1423–31.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Murakami T., Mitomi H., Saito T. et al. Distinct WNT/β-catenin signaling activation in the serrated neoplasia pathway and the adenoma-carcinoma sequence of the colorectum. Mod Pathol 2015;28:146–58.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Baker K., Zhang Y., Jin C., Jass J.R. Proximal versus distal hyperplastic polyps of the colorectum: different lesions or a biological spectrum? J Clin Pathol 2004;57:1089–93. DOI: 10.1136/jcp.2004.016600</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Frisan T. Bacterial genotoxins: тhe long journey to the nucleus of mammalian cells. Biochim Biophys Acta 2016;1858(3):567–75.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Liu C., Bettington M.L., Walker N.I. et al. CpG island methylation in sessile serrated adenomas increases with age, indicating lower risk of malignancy in young patients. J Gastroenterology 2018;155(5):1362–1365.e2. DOI: 10.1053/j.gastro.2018.07.012</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Kim Y.H., Kakar S., Cun L. et al. Distinct CpG island methylation profiles and BRAF mutation status in serrated and adenomatous colorectal polyps. Int J Cancer 2008;123:2587–93.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Bettington M., Walker N., Rosty C. et al. Clinicopathological and molecular features of sessile serrated adenomas with dysplasia or carcinoma. Gut 2017;66(1):97–106. DOI: 10.1136/gutjnl-2015-310456</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Fernando W.C., Miranda M.S., Worthley D.L. et al. CIMP phenotype in BRAF mutant serrated polyps from a prospective colonoscopy patient cohort. Gastroenterol Res Pract 2014;2014:374926. DOI: 10.1155/2014/374926</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Bosman F.T. Molecular Pathology of Colorectal Cancer. In: Molecular Surgical Pathology. New York: Springer Science + Business Media, 2013. Pp. 1–16.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Bettington M.L., Walker N.I., Rosty C. et al. A clinicopathological and molecular analysis of 200 traditional serrated adenomas. Mod Pathol 2015;28(3):414–27. DOI: 10.1038/modpathol.2014.122</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Wiland H.O., Shadrach B., Allende D. et al. Morphologic and molecular characterization of traditional serrated adenomas of the distal colon and rectum. Am J Surg Pathol 2014;38(9):1290–7. DOI: 10.1097/PAS.0000000000000253</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Tsai J.H., Liau J.Y., Lin Y.L. et al. Traditional serrated adenoma has two pathways of neoplastic progression that are distinct from the sessile serrated pathway of colorectal carcinogenesis. Mod Pathol 2014;27(10):1375–85. DOI: 10.1038/modpathol.2014.35</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Bettington M., Rosty C., Whitehall V. et al. A morphological and molecular study of proposed early forms of traditional serrated adenoma. Histopathology 2018;73(6):1023–9. DOI: 10.1111/his.13714</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Hashimoto T., Tanaka Y., Ogawa R. et al. Superficially serrated adenoma: a proposal for a novel subtype of colorectal serrated lesion. Mod Pathol 2018;31(10):1588–98. DOI: 10.1038/s41379-018-0069-8</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Hashimoto T., Yamashita S., Yoshida H. et al. WNT pathway gene mutations are associated with the presence of dysplasia in colorectal sessile serrated adenoma/polyps. Am J Surg Pathol 2017;41(9):1188–97. DOI: 10.1097/PAS.0000000000000877</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Sheridan T., Fenton H., Lewin M. et al. Sessile serrated adenomas with low- and high-grade dysplasia and early carcinomas: an immunohistochemical study of serrated lesions “caught in the act”. Am J Clin Pathol 2006;126(4):564–71. DOI: 10.1309/C7JE8BVL8420V5VT</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Oh K., Redston M., Odze R. Support for hMLH1 and MGMT silencing as a mechanism of tumorigenesis in the hyperplasticadenoma-carcinoma (serrated) carcinogenic pathway in the colon. Hum Pathol 2005;36(1):101–11. DOI: 10.1016/j.humpath.2004.10.008</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Fennell L.J., Jamieson S., McKeone D. et al. MLH1-93 G/a polymorphism is associated with MLH1 promoter methylation and protein loss in dysplastic sessile serrated adenomas with BRAFV600E mutation. BMC Cancer 2018;18(1):35. DOI: 10.1186/s12885-017-3946-5</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Kriegl L., Neumann J., Vieth M. et al. Up and downregulation of p16(Ink4a) expression in BRAF-mutated polyps/adenomas indicates a senescence barrier in the serrated route to colon cancer. Mod Pathol 2011;24(7):1015–22. DOI: 10.1038/modpathol.2011.43</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Carr N.J., Mahajan H., Tan K.L. et al. Serrated and non-serrated polyps of the colorectum: their prevalence in an unselected case series and correlation of BRAF mutation analysis with the diagnosis of sessile serrated adenoma. J Clin Pathol 2009;62(6):516–8. DOI: 10.1136/jcp.2008.061960</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Crockett S.D., Nagtegaal I.D. Terminology, molecular features, epidemiology, and management of serrated colorectal neoplasia. Gastroenterology 2019;157(4):949–966.e4. DOI: 10.1053/j.gastro.2019.06.041</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Edelstein D., Axilbund J., Hylind L. et al. Serrated polyposis: rapid and relentless development of colorectal neoplasia. Gut 2013;62(3):404–8. DOI: 10.1136/gutjnl-2011-300514</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Stanich P.P., Pearlman R. Hereditary or Not? Understanding serrated polyposis syndrome. Curr Treat Options Gastroenterol 2019;17(4):692–701. DOI: 10.1007/s11938-019-00256-z</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Gala M.K., Mizukami Y., Le L.P. et al. Germline mutations in oncogene-induced senescence pathways are associated with multiple sessile serrated adenomas. Gastroenterology 2014;146(2):520–9. DOI: 10.1053/j.gastro.2013.10.045</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Buchanan D.D., Clendenning M., Zhuoer L. et al. Lack of evidence for germline RNF43 mutations in patients with serrated polyposis syndrome from a large multinational study. Genetics of Colonic Polyposis Study. Gut 2017;66(6):1170–2. DOI: 10.1136/gutjnl-2016-312773</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Yan H.H.N., Lai J.C.W., Ho S.L. et al. RNF43 germline and somatic mutation in serrated neoplasia pathway and its association with BRAF mutation. Gut 2017;66(9):1645–56. DOI: 10.1136/gutjnl-2016-311849</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Win A.K., Walters R.J., Buchanan D.D. et al. Cancer risks for relatives of patients with serrated polyposis. Am J Gastroenterol 2012;107(5):770–8. DOI: 10.1038/ajg.2012.52</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Ijspeert J.E., Rana S.A., Atkinson N.S. et al. Clinical risk factors of colorectal cancer in patients with serrated polyposis syndrome: a multicentre cohort analysis. Dutch workgroup serrated polyps &amp; polyposis (WASP). Gut 2017;66(2):278–84. DOI: 10.1136/gutjnl-2015-310630</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Carballal S., Rodr guez-Alcalde D., Moreira L. et al. Colorectal cancer risk factors in patients with serrated polyposis syndrome: a large multicentre study. Gastrointestinal Oncology Group of the Spanish Gastroenterological Association. Gut 2016;65(11):1829–37. DOI: 10.1136/gutjnl-2015-30964</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Rosty C., Walsh M.D., Walters R.J. et al. Multiplicity and molecular heterogeneity of colorectal carcinomas in individuals with serrated polyposis. Am J Surg Pathol 2013;37(3):434–42. DOI: 10.1097/PAS.0b013e318270f748</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Veselov V.V. Serrated lesions of the colon. Dokazatelnaya gastroenterologiya 2016;5(4):27. DOI: 10.17116/dokgastro20165427-35</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Sano Y., Ikematsu H. Fu K. et al. Meshed capillary vessels by use of narrow-band imaging for differential diagnosis of small colorectal polyps. Gastrointestinal Endosc 2009;69:278–83.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Longacre T.A., Fenoglio-Preiser C.M. Mixed hyperplastic adenomatous polyps/serrated adenoma. Am J Surg Pathol 1990;14:524–37. DOI: 10.1097/00000478-199006000-00003</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Torlakovic E., Skovlund E., Snover D.C. et al. Morphologic reappraisal of serrated colorectal polyps. Am J Surg Pathol 2003;27:65–81.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Goldstein N.S., Bhanot P., Odish E., Hunter S. Hyperplastic-like colon polyps that preceded microsatellite-unstable adenocarcinomas. Am J Clin Pathol 2003;119:778–96. DOI: 10.1309/drfq0wfuf1g13ctk</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Harvey N.T., Ruszkiewicz A. Serrated neoplasia of the colorectum. World J Gastroenterol 2007;13:3792–8. DOI: 10.3748/wjg.v13.i28.3792</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Backhed F., Ding H., Wang T. et al. The gut microbiota as an environmental factor that regulates fat storage. Proc Natl Acad Sci USA 2004;101(44):15718–23.</mixed-citation></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">Zimmerman Ya.S. Eubiosis and dysbiosis of the gastrointestinal tract: myths and realities. Klinicheskaya meditsina = Clinical Medicine 2013;91(1):4–11. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">Циммерман Я.С. Эубиоз и дисбиоз желудочно-кишечного тракта: мифы и реалии. Клиническая медицина 2013;91(1):4–11.</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><mixed-citation>Coker O.O., Nakatsu G., Zhenwei Dai R. et al. Enteric fungal microbiota dysbiosis and ecological alterations in colorectal cancer. Gut 2019;68(4):654–62. DOI: 10.1136/gutjnl-2018-317178</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Dzutsev A., Goldszmid R.S., Viaud S. et al. the role of the microbiota in inflammation, carcinogenesis, and cancer therapy. Eur J Immunol 2015;45(1):17.</mixed-citation></ref></ref-list></back></article>
