<?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">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">10.24060/2076-3093-2019-9-4-297-304</article-id><article-id custom-type="elpub" pub-id-type="custom">surgonco-439</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>Экзосомальные длинные некодирующие РНК как биомаркеры и терапевтические мишени при раке</article-title><trans-title-group xml:lang="en"><trans-title>Exosomal Long NonCoding Rnas as Cancer Biomarkers and Therapeutic Targets</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-6149-5460</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Бейлерли</surname><given-names>О. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Beylerli</surname><given-names>O. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Бейлерли Озал Арзуман оглы — аспирант кафедры урологии с курсом ИДПО</p><p>450008, Уфа, ул. Ленина, 3</p></bio><bio xml:lang="en"><p>Beylerli Ozal Arzuman — Post-graduate student of the Department of Urology with the Course of Additional Professional Education</p><p>3 Lenin str., Ufa, 450008</p></bio><email xlink:type="simple">obeylerli@mail.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4965-0835</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Гареев</surname><given-names>И. Ф.</given-names></name><name name-style="western" xml:lang="en"><surname>Gareev</surname><given-names>I. F.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Гареев Ильгиз Фанилевич — аспирант кафедры нейрохирургии и медицинской реабилитации с курсом ИДПО</p><p>450008, Уфа, ул. Ленина, 3</p></bio><bio xml:lang="en"><p>Gareev Ilgiz Fanilevich — Post-graduate student of the Department of Neurosurgery and Medical Rehabilitation with the Course of Additional Professional Education</p><p>3 Lenin str., Ufa, 450008</p></bio><email xlink:type="simple">ilgiz_gareev@mail.ru</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., член-кор РАН, профессор, ректор, зав. кафедрой урологии с курсом ИДПО</p><p>450008, Уфа, ул. Ленина, 3</p></bio><bio xml:lang="en"><p>Pavlov Valentin Nikolaevich — Doctor of Medical Sciences, Corresponding Member of the Russian Academy of Sciences, Rector, Head of the Department of Urology with the Course of Additional Professional Education</p><p>3 Lenin str., Ufa, 450008</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Shiguang</surname><given-names>Zhao</given-names></name><name name-style="western" xml:lang="en"><surname>Shiguang</surname><given-names>Zhao</given-names></name></name-alternatives><bio xml:lang="ru"><p>Shiguang Zhao — профессор, зав. кафедрой нейрохирургии</p><p>150081, Хэйлунцзян, Харбин, Наньган, Баоцзянь-роуд, 157</p></bio><bio xml:lang="en"><p>Shiguang Zhao — Professor, Head of the Department of Neurosurgery</p><p>157 Baojian Rd, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, 150081</p></bio><email xlink:type="simple">guangsz@hotmail.com</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Xin</surname><given-names>Chen</given-names></name><name name-style="western" xml:lang="en"><surname>Xin</surname><given-names>Chen</given-names></name></name-alternatives><bio xml:lang="ru"><p>Xin Chen — ассистент кафедры нейрохирургии, врач-фармаколог</p><p>150081, Хэйлунцзян, Харбин, Наньган, Баоцзянь-роуд, 157 </p></bio><bio xml:lang="en"><p>Xin Chen — Assistant lecturer of the Department of Neurosurgery, Pharmacologist</p><p>157 Baojian Rd, Nangang Qu, Haerbin Shi, Heilongjiang Sheng, 150081</p></bio><email xlink:type="simple">chenxin_tracy@yeah.net</email><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-2444-9104</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кудряшов</surname><given-names>В. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kudriashov</surname><given-names>V. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кудряшов Валентин Вадимович — аспирант отделения гастроэнтерологии</p><p>610065, провинция Сычуань, Чэнду, Йихуан-роуд</p></bio><bio xml:lang="en"><p>Kudriashov Valentin Vadimovich — Post-graduate student of the Department of Gastroenterology</p><p>Yihuan Road, Chengdu, Sichuan province, 610065</p></bio><email xlink:type="simple">vkudryashov.uro@gmail.com</email><xref ref-type="aff" rid="aff-3"/></contrib></contrib-group><aff-alternatives id="aff-1"><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-2"><aff xml:lang="ru"><institution>Харбинский медицинский университет</institution><country>Китай</country></aff><aff xml:lang="en"><institution>Harbin Medical University</institution><country>China</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Западный китайский госпиталь Сычуаньского университета</institution><country>Китай</country></aff><aff xml:lang="en"><institution>West China Hospital of Sichuan University</institution><country>China</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>24</day><month>01</month><year>2020</year></pub-date><volume>9</volume><issue>4</issue><fpage>297</fpage><lpage>304</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Бейлерли О.А., Гареев И.Ф., Павлов В.Н., Shiguang Z., Xin C., Кудряшов В.В., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Бейлерли О.А., Гареев И.Ф., Павлов В.Н., Shiguang Z., Xin C., Кудряшов В.В.</copyright-holder><copyright-holder xml:lang="en">Beylerli O.A., Gareev I.F., Pavlov V.N., Shiguang Z., Xin C., Kudriashov V.V.</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/439">https://www.surgonco.ru/jour/article/view/439</self-uri><abstract><p>Обширное изучение внеклеточных везикул началось примерно десять лет назад. Экзосомы — это внеклеточные мембранные везикулы диаметром 30–100 нм, которые секретируются различными типами клеток и присутствуют в большинстве биологических жидкостей. Долгое время считались нефункциональными клеточными компонентами, а на сегодняшний день уже доказано, что являются средством межклеточного обмена информацией. Они могут перемещать биоактивные молекулы, такие как белки, липиды, РНК и ДНК. Несколько исследований показали, что их содержимое, включая белки и некодирующие нуклеиновые кислоты, могут представлять особый интерес в качестве биомаркеров заболеваний. Из этих молекул наиболее привлекательными являются некодирующие РНК (нкРНК), включая микроРНК и длинные некодирующие РНК (lncRNA). LncRNAs являются большой группой некодирующих РНК (ncRNAs) длиной более 200 нуклеотидов. LncRNAs как факторы регуляции играют важную роль в сложных клеточных процессах, таких как апоптоз, рост, дифференцировка, пролиферация и т. д. Несмотря на многие достижения в области диагностики и терапии (хирургия, лучевая терапия, химиотерапия), рак по-прежнему остается одной из наиболее важных проблем общественного здравоохранения во всем мире. С каждым днем все лучше описывается роль экзосом в развитии рака и метастазировании. Жидкостная биопсия была разработана для выявления рака на ранней стадии на основе минимально инвазивных и серийных исследований жидкости организма с преимуществом отслеживания развития опухоли в режиме реального времени. Фактически были обнаружены циркулирующие lncRNAs в экзосомах, которые подтвердили, что они тесно связаны с онкогенезом, метастазированием и терапией. В этом материале мы представляем обзор текущих исследований функциональной роли экзосомальных lncRNAs при раке и обсуждаем их потенциальное клиническое применение в качестве диагностических биомаркеров и терапевтических мишеней для рака.</p></abstract><trans-abstract xml:lang="en"><p>Extensive study of extracellular vesicles began about ten years ago. Exosomes are extracellular membrane vesicles 30–100 nm in diameter secreted by various types of cells and present in most biological fluids. For a long time they were considered non-functional cellular components. However, it has been proven that they serve as a means of intercellular exchange of information. They can move bioactive molecules such as proteins, lipids, RNA, and DNA. Several studies have shown that their contents, including proteins and non-coding nucleic acids, may be of particular interest as biomarkers of diseases. The most promising of all these molecules are non-coding RNAs (ncRNAs), including microRNAs and long non-coding RNAs (lncRNAs). LncRNAs are a large group of non-coding RNAs (ncRNAs) longer than 200 nucleotides. As regulatory factors lncRNAs play an important role in complex cellular processes, such as apoptosis, growth, differentiation, proliferation, etc. Despite many advances in diagnosis and treatment (surgery, radiation therapy, chemotherapy), cancer remains one of the most important public healthcare problems worldwide. Every day brings a better understanding of the role of exosomes in the development of cancer and metastases. Liquid biopsy has been developed as a method for the detection of cancer at an early stage. This is a series of minimally invasive tests of bodily fluids offering the advantage of real-time tracking of the tumour development. In fact, circulating exosomal lncRNAs have been found to be closely linked to processes of oncogenesis, metastasis and treatment. In this paper we review current studies into the functional role of exosomal lncRNAs in cancer and discuss their potential clinical use as diagnostic biomarkers and therapeutic targets for cancer.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>экзосомы</kwd><kwd>некодирующие РНК</kwd><kwd>длинные некодирующие РНК</kwd><kwd>микроРНК</kwd><kwd>новообразования</kwd><kwd>биомаркеры новообразования</kwd><kwd>межклеточный обмен</kwd></kwd-group><kwd-group xml:lang="en"><kwd>exosomes</kwd><kwd>noncoding RNA</kwd><kwd>long noncoding RNA</kwd><kwd>microRNAs</kwd><kwd>neoplasms</kwd><kwd>tumour biomarkers</kwd><kwd>intercellular exchange</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">Kalluri R. The biology and function of exosomes in cancer. J Clin Invest. 2016;126(4):1208–15. DOI: 10.1172/JCI81135</mixed-citation><mixed-citation xml:lang="en">Kalluri R. The biology and function of exosomes in cancer. J Clin Invest. 2016;126(4):1208–15. DOI: 10.1172/JCI81135</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Tomasetti M., Lee W., Santarelli L., Neuzil J. Exosome-derived microRNAs in cancer metabolism: possible implications in cancer diagnostics and therapy. Exp Mol Med. 2017;49(1):e285. DOI: 10.1038/ emm.2016.153</mixed-citation><mixed-citation xml:lang="en">Tomasetti M., Lee W., Santarelli L., Neuzil J. Exosome-derived microRNAs in cancer metabolism: possible implications in cancer diagnostics and therapy. Exp Mol Med. 2017;49(1):e285. DOI: 10.1038/ emm.2016.153</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Raposo G., Stoorvogel W. Extracellular vesicles: exosomes, microvesicles, and friends. J Cell Biol. 2013;200(4):373–83. DOI: 10.1083/jcb.201211138</mixed-citation><mixed-citation xml:lang="en">Raposo G., Stoorvogel W. Extracellular vesicles: exosomes, microvesicles, and friends. J Cell Biol. 2013;200(4):373–83. DOI: 10.1083/jcb.201211138</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Chettimada S., Lorenz D.R., Misra V., Dillon S.T., Reeves R.K., Manickam C., et al. Exosome markers associated with immune activation and oxidative stress in HIV patients on antiretroviral therapy. Sci Rep. 2018;8(1):7227. DOI: 10.1038/s41598-018-25515-4</mixed-citation><mixed-citation xml:lang="en">Chettimada S., Lorenz D.R., Misra V., Dillon S.T., Reeves R.K., Manickam C., et al. Exosome markers associated with immune activation and oxidative stress in HIV patients on antiretroviral therapy. Sci Rep. 2018;8(1):7227. DOI: 10.1038/s41598-018-25515-4</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">King H.W., Michael M.Z., Gleadle J.M. Hypoxic enhancement of exosome release by breast cancer cells. BMC Cancer. 2012;12:421. DOI: 10.1186/1471-2407-12-421</mixed-citation><mixed-citation xml:lang="en">King H.W., Michael M.Z., Gleadle J.M. Hypoxic enhancement of exosome release by breast cancer cells. BMC Cancer. 2012;12:421. DOI: 10.1186/1471-2407-12-421</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Sun Z., Shi K., Yang S., Liu J., Zhou Q., Wang G., et al. Effect of exosomal miRNA on cancer biology and clinical applications. Mol Cancer. 2018;17(1):147. DOI: 10.1186/s12943-018-0897-7</mixed-citation><mixed-citation xml:lang="en">Sun Z., Shi K., Yang S., Liu J., Zhou Q., Wang G., et al. Effect of exosomal miRNA on cancer biology and clinical applications. Mol Cancer. 2018;17(1):147. DOI: 10.1186/s12943-018-0897-7</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Melo S.A., Sugimoto H., O’Connell J.T., Kato N., Villanueva A., Vidal A., et al. Cancer exosomes perform cell-independent microRNA biogenesis and promote tumorigenesis. Cancer Cell. 2014;26(5):707–21. DOI: 10.1016/j.ccell.2014.09.005</mixed-citation><mixed-citation xml:lang="en">Melo S.A., Sugimoto H., O’Connell J.T., Kato N., Villanueva A., Vidal A., et al. Cancer exosomes perform cell-independent microRNA biogenesis and promote tumorigenesis. Cancer Cell. 2014;26(5):707–21. DOI: 10.1016/j.ccell.2014.09.005</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Peinado H., Aleckovic M., Lavotshkin S., Matei I., Costa-Silva B., Moreno-Bueno G., et al. Melanoma exosomes educate bone marrow progenitor cells toward a pro-metastatic phenotype through MET. Nat Med. 2012;18(6):883–91. DOI: 10.1038/nm.2753</mixed-citation><mixed-citation xml:lang="en">Peinado H., Aleckovic M., Lavotshkin S., Matei I., Costa-Silva B., Moreno-Bueno G., et al. Melanoma exosomes educate bone marrow progenitor cells toward a pro-metastatic phenotype through MET. Nat Med. 2012;18(6):883–91. DOI: 10.1038/nm.2753</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Ogawa Y., Kanai-Azuma M., Akimoto Y., Kawakami H., Yanoshita R. Exosome-like vesicles with dipeptidyl peptidase IV in human saliva. Biol Pharm Bull. 2008;31(6):1059–62. DOI: 10.1248/bpb.31.1059</mixed-citation><mixed-citation xml:lang="en">Ogawa Y., Kanai-Azuma M., Akimoto Y., Kawakami H., Yanoshita R. Exosome-like vesicles with dipeptidyl peptidase IV in human saliva. Biol Pharm Bull. 2008;31(6):1059–62. DOI: 10.1248/bpb.31.1059</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Fu Y., Li C., Luo Y., Li L., Liu J., Gui R. Silencing of long non-coding RNA MIAT sensitizes lung cancer cells to gefitinib by epigenetically regulating miR-34a. Front Pharmacol. 2018;9;82. DOI: 10.3389/fphar.2018.00082</mixed-citation><mixed-citation xml:lang="en">Fu Y., Li C., Luo Y., Li L., Liu J., Gui R. Silencing of long non-coding RNA MIAT sensitizes lung cancer cells to gefitinib by epigenetically regulating miR-34a. Front Pharmacol. 2018;9;82. DOI: 10.3389/fphar.2018.00082</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Cai T., Liu Y., Xiao J. Long noncoding RNA MALAT1 knockdown reverses chemoresistance to temozolomide via promoting microRNA-101 in glioblastoma. Cancer Medicine. 2018;7(4);1404–15. DOI: 10.1002/cam4.1384</mixed-citation><mixed-citation xml:lang="en">Cai T., Liu Y., Xiao J. Long noncoding RNA MALAT1 knockdown reverses chemoresistance to temozolomide via promoting microRNA-101 in glioblastoma. Cancer Medicine. 2018;7(4);1404–15. DOI: 10.1002/cam4.1384</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Pang Y., Mao C., Liu S. Encoding activities of non-coding RNAs. Theranostics. 2018;8(9);2496–507. DOI: 10.7150/thno.24677</mixed-citation><mixed-citation xml:lang="en">Pang Y., Mao C., Liu S. Encoding activities of non-coding RNAs. Theranostics. 2018;8(9);2496–507. DOI: 10.7150/thno.24677</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Qi P., Zhou X.Y., Du X. Circulating long non-coding RNAs in cancer: current status and future perspectives. Mol Cancer. 2016;15(1);39. DOI: 10.1186/s12943-016-0524-4</mixed-citation><mixed-citation xml:lang="en">Qi P., Zhou X.Y., Du X. Circulating long non-coding RNAs in cancer: current status and future perspectives. Mol Cancer. 2016;15(1);39. DOI: 10.1186/s12943-016-0524-4</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Enderle D., Spiel A., Coticchia C.M., Berghoff E., Mueller R., Schlumpberger M., et al. Characterization of RNA from exosomes and other extracellular vesicles isolated by a novel spin column-based method. PLoS One. 2015;10(8);e0136133. DOI: 10.1371/journal.pone.0136133</mixed-citation><mixed-citation xml:lang="en">Enderle D., Spiel A., Coticchia C.M., Berghoff E., Mueller R., Schlumpberger M., et al. Characterization of RNA from exosomes and other extracellular vesicles isolated by a novel spin column-based method. PLoS One. 2015;10(8);e0136133. DOI: 10.1371/journal.pone.0136133</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou R., Chen K.K., Zhang J., Xiao B., Huang Z., Ju C., et al. The decade of exosomal long RNA species: an emerging cancer antagonist. Mol Cancer. 2018;17(1);75. DOI: 10.1186/s12943-018-0823-z</mixed-citation><mixed-citation xml:lang="en">Zhou R., Chen K.K., Zhang J., Xiao B., Huang Z., Ju C., et al. The decade of exosomal long RNA species: an emerging cancer antagonist. Mol Cancer. 2018;17(1);75. DOI: 10.1186/s12943-018-0823-z</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Dong L., Lin W., Qi P., Xu M.D., Wu X., Ni S., et al. Circulating long RNAs in serum extracellular vesicles: their characterization and potential application as biomarkers for diagnosis of colorectal cancer. Cancer Epidemiol Biomark Prev. 2016;25(7):1158–66. DOI: 10.1158/10559965.EPI-16-0006</mixed-citation><mixed-citation xml:lang="en">Dong L., Lin W., Qi P., Xu M.D., Wu X., Ni S., et al. Circulating long RNAs in serum extracellular vesicles: their characterization and potential application as biomarkers for diagnosis of colorectal cancer. Cancer Epidemiol Biomark Prev. 2016;25(7):1158–66. DOI: 10.1158/10559965.EPI-16-0006</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Maurano M.T., Humbert R., Rynes E., Thurman R.E., Haugen E., Wang H., et al. Systematic localization of common disease-associated variation in regulatory DNA. Science. 2012;337(6099):1190–5. DOI: 10.1126/science.1222794</mixed-citation><mixed-citation xml:lang="en">Maurano M.T., Humbert R., Rynes E., Thurman R.E., Haugen E., Wang H., et al. Systematic localization of common disease-associated variation in regulatory DNA. Science. 2012;337(6099):1190–5. DOI: 10.1126/science.1222794</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Schmitt A.M., Chang H.Y. Long noncoding RNAs in cancer pathways. Cancer Cell. 2016;29(4):452–63. DOI: 10.1016/j.ccell.2016.03.010</mixed-citation><mixed-citation xml:lang="en">Schmitt A.M., Chang H.Y. Long noncoding RNAs in cancer pathways. Cancer Cell. 2016;29(4):452–63. DOI: 10.1016/j.ccell.2016.03.010</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Peng Z., Zhang C., Duan C. Functions and mechanisms of long noncoding RNAs in lung cancer. Onco Targets Ther. 2016;9;4411–24. DOI: 10.2147/OTT.S109549</mixed-citation><mixed-citation xml:lang="en">Peng Z., Zhang C., Duan C. Functions and mechanisms of long noncoding RNAs in lung cancer. Onco Targets Ther. 2016;9;4411–24. DOI: 10.2147/OTT.S109549</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Cao C., Zhang T., Zhang D., Xie L., Zou X., Lei L., et al. The long noncoding RNA, SNHG6-003, functions as a competing endogenous RNA to promote the progression of hepatocellular carcinoma. Oncogene. 2017;36(8):1112–22. DOI: 10.1038/onc.2016.278</mixed-citation><mixed-citation xml:lang="en">Cao C., Zhang T., Zhang D., Xie L., Zou X., Lei L., et al. The long noncoding RNA, SNHG6-003, functions as a competing endogenous RNA to promote the progression of hepatocellular carcinoma. Oncogene. 2017;36(8):1112–22. DOI: 10.1038/onc.2016.278</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Hu Y., Wang J., Qian J., Kong X., Tang J., Wang Y., et al. Long noncoding RNA GAPLINC regulates CD44-dependent cell invasiveness and associates with poor prognosis of gastric cancer. Cancer Res. 2014;74(23):6890–902. DOI: 10.1158/0008-5472.CAN-14-0686</mixed-citation><mixed-citation xml:lang="en">Hu Y., Wang J., Qian J., Kong X., Tang J., Wang Y., et al. Long noncoding RNA GAPLINC regulates CD44-dependent cell invasiveness and associates with poor prognosis of gastric cancer. Cancer Res. 2014;74(23):6890–902. DOI: 10.1158/0008-5472.CAN-14-0686</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Li D., Liu X., Zhou J., Hu J., Zhang D., Liu J., et al. Long noncoding RNA HULC modulates the phosphorylation of YB-1 through serving as a scaffold of extracellular signal-regulated kinase and YB-1 to enhance hepatocarcinogenesis. Hepatology. 2017;65(5):1612–27. DOI: 10.1002/hep.29010</mixed-citation><mixed-citation xml:lang="en">Li D., Liu X., Zhou J., Hu J., Zhang D., Liu J., et al. Long noncoding RNA HULC modulates the phosphorylation of YB-1 through serving as a scaffold of extracellular signal-regulated kinase and YB-1 to enhance hepatocarcinogenesis. Hepatology. 2017;65(5):1612–27. DOI: 10.1002/hep.29010</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Andrews S.J., Rothnagel J.A. Emerging evidence for functional peptides encoded by short open reading frames. Nat Rev Genet. 2014;15(3):193–204. DOI: 10.1038/nrg3520</mixed-citation><mixed-citation xml:lang="en">Andrews S.J., Rothnagel J.A. Emerging evidence for functional peptides encoded by short open reading frames. Nat Rev Genet. 2014;15(3):193–204. DOI: 10.1038/nrg3520</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Xu R., Rai A., Chen M., Suwakulsiri W., Greening D.W., Simpson R.J. Extracellular vesicles in cancer — implications for future improvements in cancer care. Nat Rev Clin Oncol. 2018;15(10):617–38. DOI: 10.1038/s41571-018-0036-9</mixed-citation><mixed-citation xml:lang="en">Xu R., Rai A., Chen M., Suwakulsiri W., Greening D.W., Simpson R.J. Extracellular vesicles in cancer — implications for future improvements in cancer care. Nat Rev Clin Oncol. 2018;15(10):617–38. DOI: 10.1038/s41571-018-0036-9</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Trajkovic K., Hsu C., Chiantia S., Rajendran L., Wenzel D., Wieland F., et al. Ceramide triggers budding of exosome vesicles into multivesicular endosomes. Science. 2008;319(5867):1244–7. DOI: 10.1126/science.1153124</mixed-citation><mixed-citation xml:lang="en">Trajkovic K., Hsu C., Chiantia S., Rajendran L., Wenzel D., Wieland F., et al. Ceramide triggers budding of exosome vesicles into multivesicular endosomes. Science. 2008;319(5867):1244–7. DOI: 10.1126/science.1153124</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Mulcahy L.A., Pink R.C., Carter D.R. Routes and mechanisms of extracellular vesicle uptake. J Extracell Vesicles. 2014;3. DOI: 10.3402/jev.v3.24641</mixed-citation><mixed-citation xml:lang="en">Mulcahy L.A., Pink R.C., Carter D.R. Routes and mechanisms of extracellular vesicle uptake. J Extracell Vesicles. 2014;3. DOI: 10.3402/jev.v3.24641</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Jin X., Chen Y., Chen H., Fei S., Chen D., Cai X., et al. Evaluation of tumor-derived exosomal miRNA as potential diagnostic biomarkers for early-stage non-small cell lung cancer using next-generation sequencing. Clin Cancer Res. 2017;23(17):5311–9. DOI: 10.1158/1078-0432.CCR-17-0577</mixed-citation><mixed-citation xml:lang="en">Jin X., Chen Y., Chen H., Fei S., Chen D., Cai X., et al. Evaluation of tumor-derived exosomal miRNA as potential diagnostic biomarkers for early-stage non-small cell lung cancer using next-generation sequencing. Clin Cancer Res. 2017;23(17):5311–9. DOI: 10.1158/1078-0432.CCR-17-0577</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Engreitz J.M., Haines J.E., Perez E.M., Munson G., Chen J., Kane M., et al. Local regulation of gene expression by lncRNA promoters, transcription and splicing. Nature. 2016;539(7629):452–5. DOI: 10.1038/nature20149</mixed-citation><mixed-citation xml:lang="en">Engreitz J.M., Haines J.E., Perez E.M., Munson G., Chen J., Kane M., et al. Local regulation of gene expression by lncRNA promoters, transcription and splicing. Nature. 2016;539(7629):452–5. DOI: 10.1038/nature20149</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Lin C., Wang Y., Wang Y., Zhang S., Yu L., Guo C., et al. Transcriptional and posttranscriptional regulation of HOXA13 by lncRNA HOTTIP facilitates tumorigenesis and metastasis in esophageal squamous carcinoma cells. Oncogene. 2017;36(38):5392–406. DOI: 10.1038/onc.2017.133</mixed-citation><mixed-citation xml:lang="en">Lin C., Wang Y., Wang Y., Zhang S., Yu L., Guo C., et al. Transcriptional and posttranscriptional regulation of HOXA13 by lncRNA HOTTIP facilitates tumorigenesis and metastasis in esophageal squamous carcinoma cells. Oncogene. 2017;36(38):5392–406. DOI: 10.1038/onc.2017.133</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Dong L., Lin W., Qi P., Xu M.D., Wu X., Ni S., et al. Circulating long RNAs in serum extracellular vesicles: their characterization and potential application as biomarkers for diagnosis of colorectal cancer. Cancer Epidemiol Biomarkers Prev. 2016;25(7):1158–66. DOI: 10.1158/10559965.EPI-16-0006</mixed-citation><mixed-citation xml:lang="en">Dong L., Lin W., Qi P., Xu M.D., Wu X., Ni S., et al. Circulating long RNAs in serum extracellular vesicles: their characterization and potential application as biomarkers for diagnosis of colorectal cancer. Cancer Epidemiol Biomarkers Prev. 2016;25(7):1158–66. DOI: 10.1158/10559965.EPI-16-0006</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Zhou R., Chen K.K., Zhang J., Xiao B., Huang Z., Ju C., et al. The decade of exosomal long RNA species: an emerging cancer antagonist. Mol Cancer. 2018;17(1):75. DOI: 10.1186/s12943-018-0823-z</mixed-citation><mixed-citation xml:lang="en">Zhou R., Chen K.K., Zhang J., Xiao B., Huang Z., Ju C., et al. The decade of exosomal long RNA species: an emerging cancer antagonist. Mol Cancer. 2018;17(1):75. DOI: 10.1186/s12943-018-0823-z</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Revenfeld A.L.S., Bæk R., Nielsen M.H., Stensballe A., Varming K., Jørgensen M. Diagnostic and prognostic potential of extracellular vesicles in peripheral blood. Clin Ther. 2014;36(6):830–46. DOI: 10.1016/j.clinthera.2014.05.008</mixed-citation><mixed-citation xml:lang="en">Revenfeld A.L.S., Bæk R., Nielsen M.H., Stensballe A., Varming K., Jørgensen M. Diagnostic and prognostic potential of extracellular vesicles in peripheral blood. Clin Ther. 2014;36(6):830–46. DOI: 10.1016/j.clinthera.2014.05.008</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">Skog J., Wurdinger T., Rijn S., Meijer D., Gainche L., Esteves M.S., et al. Glioblastoma microvesicles transport RNA and protein that promote tumor growth and provide diagnostic biomarkers. Nat Cell Biol. 2008;10(12):1470–6. DOI: 10.1038/ncb1800</mixed-citation><mixed-citation xml:lang="en">Skog J., Wurdinger T., Rijn S., Meijer D., Gainche L., Esteves M.S., et al. Glioblastoma microvesicles transport RNA and protein that promote tumor growth and provide diagnostic biomarkers. Nat Cell Biol. 2008;10(12):1470–6. DOI: 10.1038/ncb1800</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Qu L., Ding j., Cheng Chen, Zhen Jie Wu, Bing Liu, Yi Gao, et al. Exosome-transmitted lncARSR promotes sunitinib resistance in renal cancer by acting as a competing endogenous RNA. Cancer Cell. 2016;29(5);653–68. DOI: 10.1016/j.ccell.2016.03.004</mixed-citation><mixed-citation xml:lang="en">Qu L., Ding j., Cheng Chen, Zhen Jie Wu, Bing Liu, Yi Gao, et al. Exosome-transmitted lncARSR promotes sunitinib resistance in renal cancer by acting as a competing endogenous RNA. Cancer Cell. 2016;29(5);653–68. DOI: 10.1016/j.ccell.2016.03.004</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Pan L., Liang W., Fu M., Huang Z.H., Li X., Zhang W., et al. Exosomesmediated transfer of long noncoding RNA ZFAS1 promotes gastric cancer progression. J Cancer Res Clin Oncol. 2017;143(6):991–1004. DOI: 10.1007/s00432-017-2361-2</mixed-citation><mixed-citation xml:lang="en">Pan L., Liang W., Fu M., Huang Z.H., Li X., Zhang W., et al. Exosomesmediated transfer of long noncoding RNA ZFAS1 promotes gastric cancer progression. J Cancer Res Clin Oncol. 2017;143(6):991–1004. DOI: 10.1007/s00432-017-2361-2</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Wang J., Zhou Y., Lu J., Sun Y., Xiao H., Liu M., et al. Combined detection of serum exosomal miR-21 and HOTAIR as diagnostic and prognostic biomarkers for laryngeal squamous cell carcinoma. Med Oncol. 2014;31(9):148. DOI: 10.1007/s12032-014-0148-8</mixed-citation><mixed-citation xml:lang="en">Wang J., Zhou Y., Lu J., Sun Y., Xiao H., Liu M., et al. Combined detection of serum exosomal miR-21 and HOTAIR as diagnostic and prognostic biomarkers for laryngeal squamous cell carcinoma. Med Oncol. 2014;31(9):148. DOI: 10.1007/s12032-014-0148-8</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Ge X., Wang Y., Nie J., Li Q., Tang L., Deng X., et al. The diagnostic/prognostic potential and molecular functions of long non-coding RNAs in the exosomes derived from the bile of human cholangiocarcinoma. Oncotarget. 2017;25;8(41):69995–70005. DOI: 10.18632/oncotarget.19547</mixed-citation><mixed-citation xml:lang="en">Ge X., Wang Y., Nie J., Li Q., Tang L., Deng X., et al. The diagnostic/prognostic potential and molecular functions of long non-coding RNAs in the exosomes derived from the bile of human cholangiocarcinoma. Oncotarget. 2017;25;8(41):69995–70005. DOI: 10.18632/oncotarget.19547</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang J., Liu S.C., Luo X.H., Tao G.X., Guan M., Yuan H., et al. Exosomal long noncoding RNAs are differentially expressed in the cervicovaginal lavage samples of cervical cancer patients. J Clin Lab Anal. 2016;30(6):1116–21. DOI: 10.1002/jcla.21990</mixed-citation><mixed-citation xml:lang="en">Zhang J., Liu S.C., Luo X.H., Tao G.X., Guan M., Yuan H., et al. Exosomal long noncoding RNAs are differentially expressed in the cervicovaginal lavage samples of cervical cancer patients. J Clin Lab Anal. 2016;30(6):1116–21. DOI: 10.1002/jcla.21990</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Berrondo C., Flax J., Kucherov V., Siebert A., Osinski T., Rosenberg A., et al. Expression of the long non-coding RNA HOTAIR correlates with disease progression in bladder cancer and is contained in bladder cancer patient urinary exosomes. PLoS One. 2016;11(1):e0147236. DOI: 10.1371/journal.pone.0147236</mixed-citation><mixed-citation xml:lang="en">Berrondo C., Flax J., Kucherov V., Siebert A., Osinski T., Rosenberg A., et al. Expression of the long non-coding RNA HOTAIR correlates with disease progression in bladder cancer and is contained in bladder cancer patient urinary exosomes. PLoS One. 2016;11(1):e0147236. DOI: 10.1371/journal.pone.0147236</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Guo K., Yao J., Yu Q., Li Z., Huang H., Cheng J., et al. The expression pattern of long non-coding RNA PVT1 in tumor tissues and in extracellular vesicles of colorectal cancer correlates with cancer progression. Tumor Biology. 2017;39(4). DOI: 10.1177/1010428317699122</mixed-citation><mixed-citation xml:lang="en">Guo K., Yao J., Yu Q., Li Z., Huang H., Cheng J., et al. The expression pattern of long non-coding RNA PVT1 in tumor tissues and in extracellular vesicles of colorectal cancer correlates with cancer progression. Tumor Biology. 2017;39(4). DOI: 10.1177/1010428317699122</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Xue M., Chen W., Xiang A., Wang R., Chen H., Pan J., et al. Hypoxic exosomes facilitate bladder tumor growth and development through transferring long non-coding RNA-UCA1. Mol Cancer. 25;16(1):143. DOI: 10.1186/s12943-017-0714-8</mixed-citation><mixed-citation xml:lang="en">Xue M., Chen W., Xiang A., Wang R., Chen H., Pan J., et al. Hypoxic exosomes facilitate bladder tumor growth and development through transferring long non-coding RNA-UCA1. Mol Cancer. 25;16(1):143. DOI: 10.1186/s12943-017-0714-8</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">David C.J., Huang Y.H., Chen M., Su J., Zou Y., Bardeesy N., et al. TGF-β Tumor Suppression through a Lethal EMT. Cell. 2016;164(5):1015–30. DOI: 10.1016/j.cell.2016.01.009</mixed-citation><mixed-citation xml:lang="en">David C.J., Huang Y.H., Chen M., Su J., Zou Y., Bardeesy N., et al. TGF-β Tumor Suppression through a Lethal EMT. Cell. 2016;164(5):1015–30. DOI: 10.1016/j.cell.2016.01.009</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Xu C.G., Yang M.F., Ren Y.Q., Wu C.H., Wang L.Q. Exosomes mediated transfer of lncRNA UCA1 results in increased tamoxifen resistance in breast cancer cells. Eur Rev Med Pharmacol Sci. 2016;20(20):4362–8. PMID: 27831634</mixed-citation><mixed-citation xml:lang="en">Xu C.G., Yang M.F., Ren Y.Q., Wu C.H., Wang L.Q. Exosomes mediated transfer of lncRNA UCA1 results in increased tamoxifen resistance in breast cancer cells. Eur Rev Med Pharmacol Sci. 2016;20(20):4362–8. PMID: 27831634</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Dong H., Wang W., Chen R., Zhang Y., Zou K., Ye M., et al. Exosomemediated transfer of lncR-NASNHG14 promotes trastuzumab chemoresistance in breast cancer. Int J Oncol. 2018;53(3):1013–26. DOI: 10.3892/ijo.2018.4467</mixed-citation><mixed-citation xml:lang="en">Dong H., Wang W., Chen R., Zhang Y., Zou K., Ye M., et al. Exosomemediated transfer of lncR-NASNHG14 promotes trastuzumab chemoresistance in breast cancer. Int J Oncol. 2018;53(3):1013–26. DOI: 10.3892/ijo.2018.4467</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang W., Cai X., Yu J., Lu X., Qian Q., Qian W. Exosome-mediated transfer of lncRNA RP11838N2.4 promotes erlotinib resistance in nonsmall cell lung cancer. Int J Oncol. 2018;53(2):527–38. DOI: 10.3892/ijo.2018.4412</mixed-citation><mixed-citation xml:lang="en">Zhang W., Cai X., Yu J., Lu X., Qian Q., Qian W. Exosome-mediated transfer of lncRNA RP11838N2.4 promotes erlotinib resistance in nonsmall cell lung cancer. Int J Oncol. 2018;53(2):527–38. DOI: 10.3892/ijo.2018.4412</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Schmidt M., Fernandez de Mattos S., van der Horst A., Klompmaker R., Kops G.J., Lam E.W., et al. Cell cycle inhibition by FoxO forkhead transcription factors involves downregulation of cyclin D. Mol Cell Biol. 2002;22(22):7842–52. DOI: 10.1128/mcb.22.22.7842-7852.2002</mixed-citation><mixed-citation xml:lang="en">Schmidt M., Fernandez de Mattos S., van der Horst A., Klompmaker R., Kops G.J., Lam E.W., et al. Cell cycle inhibition by FoxO forkhead transcription factors involves downregulation of cyclin D. Mol Cell Biol. 2002;22(22):7842–52. DOI: 10.1128/mcb.22.22.7842-7852.2002</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Kang M., Ren M., Li Y., Fu Y., Deng M., Li C. Exosome-mediated transfer of lncRNA PART1 induces gefitinib resistance in esophageal squamous cell carcinoma via functioning as a competing endogenous RNA. J Exp Clin Cancer Res. 2018;37(1):171. DOI: 10.1186/s13046018-0845-9</mixed-citation><mixed-citation xml:lang="en">Kang M., Ren M., Li Y., Fu Y., Deng M., Li C. Exosome-mediated transfer of lncRNA PART1 induces gefitinib resistance in esophageal squamous cell carcinoma via functioning as a competing endogenous RNA. J Exp Clin Cancer Res. 2018;37(1):171. DOI: 10.1186/s13046018-0845-9</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Qu L., Ding J., Chen C., Wu Z.J., Liu B., Gao Y., et al. Exosome-transmitted lncARSR promotes sunitinib resistance in renal cancer by acting as a competing endogenous RNA. Cancer Cell. 2016;29(5):653–68. DOI: 10.1016/j.ccell.2016.03.004</mixed-citation><mixed-citation xml:lang="en">Qu L., Ding J., Chen C., Wu Z.J., Liu B., Gao Y., et al. Exosome-transmitted lncARSR promotes sunitinib resistance in renal cancer by acting as a competing endogenous RNA. Cancer Cell. 2016;29(5):653–68. DOI: 10.1016/j.ccell.2016.03.004</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Von Hoff D.D., Ervin T., Arena F.P., Chiorean E.G., Infante J., Moore M., et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N Engl J Med. 2013;369(18):1691–703. DOI: 10.1056/NEJMoa1304369</mixed-citation><mixed-citation xml:lang="en">Von Hoff D.D., Ervin T., Arena F.P., Chiorean E.G., Infante J., Moore M., et al. Increased survival in pancreatic cancer with nab-paclitaxel plus gemcitabine. N Engl J Med. 2013;369(18):1691–703. DOI: 10.1056/NEJMoa1304369</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Senthebane D.A., Rowe A., Thomford N.E., Shipanga H., Munro D., Mazeedi MAMA, et al. The role of tumor microenvironment in chemoresistance: to survive, keep your enemies closer. Int J Mol Sci. 2017;18(7):1586. DOI: 10.3390/ijms18071586</mixed-citation><mixed-citation xml:lang="en">Senthebane D.A., Rowe A., Thomford N.E., Shipanga H., Munro D., Mazeedi MAMA, et al. The role of tumor microenvironment in chemoresistance: to survive, keep your enemies closer. Int J Mol Sci. 2017;18(7):1586. DOI: 10.3390/ijms18071586</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Maemondo M., Inoue A., Kobayashi K., Sugawara S., Oizumi S., Isobe H., et al. Gefitinib or chemotherapy for non-small-cell lung cancer with mutated EGFR. N Engl J Med. 2010;362(25):2380–8. DOI: 10.1056/NEJMoa0909530</mixed-citation><mixed-citation xml:lang="en">Maemondo M., Inoue A., Kobayashi K., Sugawara S., Oizumi S., Isobe H., et al. Gefitinib or chemotherapy for non-small-cell lung cancer with mutated EGFR. N Engl J Med. 2010;362(25):2380–8. DOI: 10.1056/NEJMoa0909530</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Lei Y., Guo W., Chen B., Chen L., Gong J., Li W. Tumor-released lncRNA H19 promotes gefitinib resistance via packaging into exosomes in non‑small cell lung cancer. Oncol Rep. 2018;40(6):3438–46. DOI: 10.3892/or.2018.6762</mixed-citation><mixed-citation xml:lang="en">Lei Y., Guo W., Chen B., Chen L., Gong J., Li W. Tumor-released lncRNA H19 promotes gefitinib resistance via packaging into exosomes in non‑small cell lung cancer. Oncol Rep. 2018;40(6):3438–46. DOI: 10.3892/or.2018.6762</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Kang M., Ren M., Li Y., Fu Y., Deng M., Li C. Exosome-mediated transfer of lncRNA PART1 induces gefitinib resistance in esophageal squamous cell carcinoma via functioning as a competing endogenous RNA. J Exp Clin Cancer Res. 2018;37(1):171. DOI: 10.1186/s13046018-0845-9</mixed-citation><mixed-citation xml:lang="en">Kang M., Ren M., Li Y., Fu Y., Deng M., Li C. Exosome-mediated transfer of lncRNA PART1 induces gefitinib resistance in esophageal squamous cell carcinoma via functioning as a competing endogenous RNA. J Exp Clin Cancer Res. 2018;37(1):171. DOI: 10.1186/s13046018-0845-9</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Coelho R.C., Reinert T., Campos F., Peixoto F.A., de Andrade C.A., Castro T., et al. Sunitinib treatment in patients with advanced renal cell cancer: The Brazilian National Cancer Institute (INCA) experience. Int Braz J Urol. 2016;42(4):694–703. DOI: 10.1590/S1677-5538. IBJU.2015.0226</mixed-citation><mixed-citation xml:lang="en">Coelho R.C., Reinert T., Campos F., Peixoto F.A., de Andrade C.A., Castro T., et al. Sunitinib treatment in patients with advanced renal cell cancer: The Brazilian National Cancer Institute (INCA) experience. Int Braz J Urol. 2016;42(4):694–703. DOI: 10.1590/S1677-5538. IBJU.2015.0226</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Qu L., Ding J., Chen C., Wu Z.J., Liu B., Gao Y., et al. Exosome-transmitted lncARSR promotes sunitinib resistance in renal cancer by acting as a competing endogenous RNA. Cancer Cell. 2016;29(5):653–68. DOI: 10.1016/j.ccell.2016.03.004</mixed-citation><mixed-citation xml:lang="en">Qu L., Ding J., Chen C., Wu Z.J., Liu B., Gao Y., et al. Exosome-transmitted lncARSR promotes sunitinib resistance in renal cancer by acting as a competing endogenous RNA. Cancer Cell. 2016;29(5):653–68. DOI: 10.1016/j.ccell.2016.03.004</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Yang Y.N., Zhang R., Du J.W., Yuan H.H., Li Y., Wei X., et al. Predictive role of UCA1-containing exosomes in cetuximab-resistant colorectal cancer. Cancer Cell Int. 2018;18:164. DOI: 10.1186/s12935-018-0660-6</mixed-citation><mixed-citation xml:lang="en">Yang Y.N., Zhang R., Du J.W., Yuan H.H., Li Y., Wei X., et al. Predictive role of UCA1-containing exosomes in cetuximab-resistant colorectal cancer. Cancer Cell Int. 2018;18:164. DOI: 10.1186/s12935-018-0660-6</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Fan Q., Yang L., Zhang X., Peng X., Wei S., Su D., et al. The emerging role of exosome-derived non-coding RNAs in cancer biology. Cancer Lett. 20181;414:107–115. DOI: 10.1016/j.canlet.2017.10.040</mixed-citation><mixed-citation xml:lang="en">Fan Q., Yang L., Zhang X., Peng X., Wei S., Su D., et al. The emerging role of exosome-derived non-coding RNAs in cancer biology. Cancer Lett. 20181;414:107–115. DOI: 10.1016/j.canlet.2017.10.040</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Yang H., Fu H., Xu W., Zhang X. Exosomal non-coding RNAs: a promising cancer biomarker. Clin Chem Lab Med. 2016;1;54(12):1871–9. DOI: 10.1515/cclm-2016-0029</mixed-citation><mixed-citation xml:lang="en">Yang H., Fu H., Xu W., Zhang X. Exosomal non-coding RNAs: a promising cancer biomarker. Clin Chem Lab Med. 2016;1;54(12):1871–9. DOI: 10.1515/cclm-2016-0029</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Marrugo-Ramírez J., Mir M., Samitier J. Blood-based cancer biomarkers in liquid biopsy: a promising non-invasive alternative to tissue biopsy. Int J Mol Sci. 2018;19(10). DOI: 10.3390/ijms19102877</mixed-citation><mixed-citation xml:lang="en">Marrugo-Ramírez J., Mir M., Samitier J. Blood-based cancer biomarkers in liquid biopsy: a promising non-invasive alternative to tissue biopsy. Int J Mol Sci. 2018;19(10). DOI: 10.3390/ijms19102877</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Coumans F.A.W., Brisson A.R., Buzas E.I., Dignat-George F., Drees E.E.E., El-Andaloussi S., et al. Methodological guidelines to study extracellular vesicles. Circ Res. 2017;120(10):1632–48. DOI: 10.1161/CIRCRESAHA.117.309417</mixed-citation><mixed-citation xml:lang="en">Coumans F.A.W., Brisson A.R., Buzas E.I., Dignat-George F., Drees E.E.E., El-Andaloussi S., et al. Methodological guidelines to study extracellular vesicles. Circ Res. 2017;120(10):1632–48. DOI: 10.1161/CIRCRESAHA.117.309417</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>
