<?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">10.24060/2076-3093-2024-14-2-180-185</article-id><article-id custom-type="elpub" pub-id-type="custom">surgonco-955</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>Механизмы онкопротективных эффектов фитостеролов. Обзор литературы</article-title><trans-title-group xml:lang="en"><trans-title>Mechanisms of Cancerprotective Effects of Phytosterols. Literature Review</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-0371-0385</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Рахматуллина</surname><given-names>И. Р.</given-names></name><name name-style="western" xml:lang="en"><surname>Rakhmatullina</surname><given-names>I. R.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Рахматуллина Ирина Робинзоновна — д.м.н., профессор, кафедра онкологии и клинической морфологии</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Irina R. Rakhmatullina — Dr. Sci. (Med.), Prof., Department of Oncology and Clinical Morphology</p><p>Ufa</p></bio><email xlink:type="simple">i.r.rakhmatullina@gmail.com</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Кудашкина</surname><given-names>Н. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Kudashkina</surname><given-names>N. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кудашкина Наталья Владимировна — д.фарм.н., профессор, кафедра фармакогнозии и ботаники</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Natalya V. Kudashkina — Dr. Sci. (Pharmacy), Prof., Department of Pharmacognosy and Botany</p><p>Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-1360-8125</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Фролова</surname><given-names>В. Ю.</given-names></name><name name-style="western" xml:lang="en"><surname>Frolova</surname><given-names>V. Yu.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Фролова Вероника Юрьевна — к.м.н., кафедра онкологии и клинической морфологии, поликлиника</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Veronika Yu. Frolova — Cand. Sci. (Med.), Department of Oncology and Clinical Morphology, Outpatient Clinic</p><p>Ufa</p></bio><xref ref-type="aff" rid="aff-2"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0009-3746-8225</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Озиева</surname><given-names>М. Х.</given-names></name><name name-style="western" xml:lang="en"><surname>Ozieva</surname><given-names>M. Kh.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Озиева Мадина Хасановна — к.м.н., кафедра госпитальной хирургии, Центр амбулаторной онкологической помощи</p><p>Магас</p><p>Назрань</p></bio><bio xml:lang="en"><p>Madina Kh. Ozieva — Cand. Sci. (Med.), Department of Hospital Surgery, Outpatient Oncological Care Center</p><p>Magas</p><p>Nazran</p></bio><xref ref-type="aff" rid="aff-3"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0009-0006-9416-1228</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Садыков</surname><given-names>Б. И.</given-names></name><name name-style="western" xml:lang="en"><surname>Sadykov</surname><given-names>B. I.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Садыков Булат Ильдарович — ординатор, кафедра онкологии и клинической морфологии</p><p>Республика Башкортостан, Уфа</p></bio><bio xml:lang="en"><p>Bulat I. Sadykov — Resident, Department of Oncology and Clinical Morphology</p><p>Ufa</p></bio><xref ref-type="aff" rid="aff-1"/></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>Башкирский государственный медицинский университет; Республиканский клинический онкологический диспансер</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Bashkir State Medical University; Republican Clinical Oncology Dispensary</institution><country>Russian Federation</country></aff></aff-alternatives><aff-alternatives id="aff-3"><aff xml:lang="ru"><institution>Ингушский государственный университет; Городская поликлиника</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Ingush State University; City Clinic</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2024</year></pub-date><pub-date pub-type="epub"><day>05</day><month>07</month><year>2024</year></pub-date><volume>14</volume><issue>2</issue><fpage>180</fpage><lpage>185</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Рахматуллина И.Р., Кудашкина Н.В., Фролова В.Ю., Озиева М.Х., Садыков Б.И., 2024</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="ru">Рахматуллина И.Р., Кудашкина Н.В., Фролова В.Ю., Озиева М.Х., Садыков Б.И.</copyright-holder><copyright-holder xml:lang="en">Rakhmatullina I.R., Kudashkina N.V., Frolova V.Y., Ozieva M.K., Sadykov B.I.</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/955">https://www.surgonco.ru/jour/article/view/955</self-uri><abstract><p>Онкологические заболевания являются второй причиной смертности в  Российской Федерации. Продление жизни пациентов с  онкологической патологией предусматривает лечение токсическими препаратами с  множественными побочными явлениями. Сегодня ученые всего мира стремятся найти препараты без токсических явлений. Мы обратились к  фитостеролам. Фитостеролы  — это класс стероидов, широко распространенных в растениях как важный компонент мембран растительных клеток. К ним относятся стигмастерол, бета-ситостерол, кампестерол. При раке печени было найдено, что стигмастерол повышает экспрессию проапоптотических генов (Bax, p53) и снижает экспрессию антиапоптотического гена Bcl-2 в клетках рака печени HepG2. Стигмастерол способен вызывать остановку клеток в фазе G0-G1 (стационарная фаза), в результате чего в фазе G2/M (фаза деления) оказывается намного меньше клеток. Стигмастерол индуцирует апоптоз и защитную аутофагию в  клетках рака желудка, ингибируя при этом сигнальный путь Akt/mTOR. β-ситостерол проявляет ингибирующее рост и  цитотоксическое действие против ряда установленных линий раковых клеток in  vitro и in vivo, но не вызывает острых/подострых токсических эффектов. β-ситостерол широко используется для лечения хронических заболеваний предстательной железы. В  США за  2020  год потребители с  этой целью потратили 24 827 065  долларов на  биологически активные добавки, содержащие бета-ситостерол. Кампестерол индуцирует апоптоз клеток через митохондриальный путь. Кампестерол цитотоксичен по отношению к клеткам U937 гепатоцеллюлярного рака. Кампестерол вызывает апоптоз клеток и активирует проапоптотические сигналы в клеточных линиях рака яичников человека. В данном обзоре литературы мы убедительно показали, что конкретные вещества этой группы — бета-ситостерол, стигмастерол и кампестерол — обладают выраженным противоопухолевым эффектом.</p></abstract><trans-abstract xml:lang="en"><p>Cancer is recognized as the second leading cause of mortality in the Russian Federation. Prolonging the life of oncology patients involves treatment with toxic drugs, causing multiple side effects. Today, scientists around the world are striving to find non-toxic drugs. The present study explores phytosterols. Phytosterols refer to a class of steroids widely distributed in plants as an essential component of plant cell membranes. They include stigmasterol, beta-sitosterol, and campesterol. Stigmasterol has been found to increase the expression of proapoptotic genes (Bax, p53) and decrease the expression of the antiapoptotic gene Bcl-2 in HepG2 liver cancer cells. Stigmasterol is able to induce cell arrest in G0-G1 phase (stationary phase), resulting in fewer cells in the G2/M phase (division phase). It induces apoptosis and protective autophagy in gastric cancer cells while inhibiting the Akt/mTOR signaling pathway. β-sitosterol exhibits growth inhibitory and cytotoxic effects against a number of established cancer cell lines in vitro and in vivo, and remains free from acute/subacute toxic effects. β-sitosterol is widely used to treat chronic prostate diseases. In 2020, spendings on dietary supplements rich in beta-sitosterol accounted for $24 827 065 in the USA. Campesterol induces cell apoptosis via the mitochondrial pathway. It appears cytotoxic to U937 hepatocellular cancer cells. Campesterol induces cell apoptosis and activates proapoptotic signaling in ovarian cancer cell lines of a person. The present literature review demonstrates that specific substances in this group, beta-sitosterol, stigmasterol, and campesterol, provide pronounced antitumor effects.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>фитостеролы</kwd><kwd>фитостерины</kwd><kwd>рак</kwd><kwd>новообразования</kwd><kwd>противоопухолевая активность</kwd><kwd>бета-ситостерол</kwd><kwd>стигмастерол</kwd><kwd>кампестерол</kwd></kwd-group><kwd-group xml:lang="en"><kwd>phytosterols</kwd><kwd>phytosterin</kwd><kwd>cancer</kwd><kwd>neoplasms</kwd><kwd>antitumor activity</kwd><kwd>beta-sitosterol</kwd><kwd>stigmasterol</kwd><kwd>campesterol</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">Ганцев Ш.Х., Ганцев К.Ш., Кайдарова Д.Р., Кзыргалин Ш.Р., Кобяков Г.Л., Кудайбергенова И.О. и др. Онкология. М.: ГЭОТАР; 2023.</mixed-citation><mixed-citation xml:lang="en">Gantsev Sh.Kh., Gantsev K.Sh., Kaydarova D.R., Kzyrgalin Sh.R., Kobyakov G.L., Kudaibergenova I.O., et al. Oncology. Moscow: GEOTAR; 2023 (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Sonawane P.D., Pollier J., Panda S., Szymanski J., Massalha H., Yona M., et al. Plant cholesterol biosynthetic pathway overlaps with phytosterol metabolism. Nat Plants. 2016;3:16205. DOI: 10.1038/nplants.2016.205</mixed-citation><mixed-citation xml:lang="en">Sonawane P.D., Pollier J., Panda S., Szymanski J., Massalha H., Yona M., et al. Plant cholesterol biosynthetic pathway overlaps with phytosterol metabolism. Nat Plants. 2016;3:16205. DOI: 10.1038/nplants.2016.205</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Bansal R., Sen S.S., Muthuswami R., Madhubala R. Stigmasterol as a potential biomarker for amphotericin B resistance in Leishmania donovani. J Antimicrob Chemother. 2020;75(4):942–50. DOI: 10.1093/jac/dkz515</mixed-citation><mixed-citation xml:lang="en">Bansal R., Sen S.S., Muthuswami R., Madhubala R. Stigmasterol as a potential biomarker for amphotericin B resistance in Leishmania donovani. J Antimicrob Chemother. 2020;75(4):942–50. DOI: 10.1093/jac/dkz515</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Zhang X., Wang J., Zhu L., Wang X., Meng F., Xia L., et al. Advances in Stigmasterol on its anti-tumor effect and mechanism of action. Front Oncol. 2022;12:1101289. DOI: 10.3389/fonc.2022.1101289</mixed-citation><mixed-citation xml:lang="en">Zhang X., Wang J., Zhu L., Wang X., Meng F., Xia L., et al. Advances in Stigmasterol on its anti-tumor effect and mechanism of action. Front Oncol. 2022;12:1101289. DOI: 10.3389/fonc.2022.1101289</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Kim Y.S., Li X.F., Kang K.H., Ryu B., Kim S.K. Stigmasterol isolated from marine microalgae Navicula incerta induces apoptosis in human hepatoma HepG2 cells. BMB Rep. 2014;47(8):433–8. DOI: 10.5483/bmbrep.2014.47.8.153</mixed-citation><mixed-citation xml:lang="en">Kim Y.S., Li X.F., Kang K.H., Ryu B., Kim S.K. Stigmasterol isolated from marine microalgae Navicula incerta induces apoptosis in human hepatoma HepG2 cells. BMB Rep. 2014;47(8):433–8. DOI: 10.5483/bmbrep.2014.47.8.153</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Shuo Zhang Y.W., Wang L. The inhibitory effect of stigmasterol on hepatocellular carcinoma cells in vitro and in vivo and its effect on proliferation cycle and apoptosis. Adv Modern Biomed. 2008;8(11):2016–7. DOI: 10.13241/j.cnki.pmb.2008.11.017</mixed-citation><mixed-citation xml:lang="en">Shuo Zhang Y.W., Wang L. The inhibitory effect of stigmasterol on hepatocellular carcinoma cells in vitro and in vivo and its effect on proliferation cycle and apoptosis. Adv Modern Biomed. 2008;8(11):2016–7. DOI: 10.13241/j.cnki.pmb.2008.11.017</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Dong Y., Chen C., Chen C., Zhang C., Zhang L., Zhang Y., et al. Stigmasterol inhibits the progression of lung cancer by regulating retinoic acid-related orphan receptor C. Histol Histopathol. 2021;36(12):1285– 99. DOI: 10.14670/HH-18-388</mixed-citation><mixed-citation xml:lang="en">Dong Y., Chen C., Chen C., Zhang C., Zhang L., Zhang Y., et al. Stigmasterol inhibits the progression of lung cancer by regulating retinoic acid-related orphan receptor C. Histol Histopathol. 2021;36(12):1285– 99. DOI: 10.14670/HH-18-388</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Zhao H., Zhang X., Wang M., Lin Y., Zhou S. Stigmasterol simultaneously induces apoptosis and protective autophagy by inhibiting Akt/ mTOR pathway in gastric cancer cells. Front Oncol. 2021;11. DOI :10.3389/fonc.2021.629008</mixed-citation><mixed-citation xml:lang="en">Zhao H., Zhang X., Wang M., Lin Y., Zhou S. Stigmasterol simultaneously induces apoptosis and protective autophagy by inhibiting Akt/ mTOR pathway in gastric cancer cells. Front Oncol. 2021;11. DOI: 10.3389/fonc.2021.629008</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Woyengo T.A., Ramprasath V.R., Jones P.J. Anticancer effects of phytosterols. Eur J Clin Nutr. 2009;63(7):813–20. DOI: 10.1038/ejcn.2009.29</mixed-citation><mixed-citation xml:lang="en">Woyengo T.A., Ramprasath V.R., Jones P.J. Anticancer effects of phytosterols. Eur J Clin Nutr. 2009;63(7):813–20. DOI: 10.1038/ejcn.2009.29</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Liao P.C., Lai M.H., Hsu K.P., Kuo Y.H., Chen J., Tsai M.C., et al. Identification of β-Sitosterol as in vitro anti-inflammatory constituent in Moringa oleifera. J Agric Food Chem. 2018;66(41):10748–59. DOI: 10.1021/acs.jafc.8b04555</mixed-citation><mixed-citation xml:lang="en">Liao P.C., Lai M.H., Hsu K.P., Kuo Y.H., Chen J., Tsai M.C., et al. Identification of β-Sitosterol as in vitro anti-inflammatory constituent in Moringa oleifera. J Agric Food Chem. 2018;66(41):10748–59. DOI: 10.1021/acs.jafc.8b04555</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Gupta M.B., Nath R., Srivastava N., Shanker K., Kishor K., Bhargava K.P. Anti-inflammatory and antipyretic activities of beta-sitosterol. Planta Med. 1980;39(2):157–63. DOI: 10.1055/s-2008-1074919</mixed-citation><mixed-citation xml:lang="en">Gupta M.B., Nath R., Srivastava N., Shanker K., Kishor K., Bhargava K.P. Anti-inflammatory and antipyretic activities of beta-sitosterol. Planta Med. 1980;39(2):157–63. DOI: 10.1055/s-2008-1074919</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Nirmal S.A., Pal S.C., Mandal S.C., Patil A.N. Analgesic and antiinflammatory activity of β-sitosterol isolated from Nyctanthes arbortristis leaves. Inflammopharmacology. 2012;20:219–24. DOI: 10.1007/s10787-011-0110-8</mixed-citation><mixed-citation xml:lang="en">Nirmal S.A., Pal S.C., Mandal S.C., Patil A.N. Analgesic and antiinflammatory activity of β-sitosterol isolated from Nyctanthes arbortristis leaves. Inflammopharmacology. 2012;20:219–24. DOI: 10.1007/s10787-011-0110-8</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Babu S., Jayaraman S. An update on β-sitosterol: A potential herbal nutraceutical for diabetic management. Biomed Pharmacother. 2020;131:110702. DOI: 10.1016/j.biopha.2020.110702</mixed-citation><mixed-citation xml:lang="en">Babu S., Jayaraman S. An update on β-sitosterol: A potential herbal nutraceutical for diabetic management. Biomed Pharmacother. 2020;131:110702. DOI: 10.1016/j.biopha.2020.110702</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Bin Sayeed M.S., Ameen S.S. Beta-Sitosterol: a promising but orphan nutraceutical to fight against cancer. Nutr Cancer. 2015;67(8):1214–20. DOI: 10.1080/01635581.2015.1087042</mixed-citation><mixed-citation xml:lang="en">Bin Sayeed M.S., Ameen S.S. Beta-Sitosterol: a promising but orphan nutraceutical to fight against cancer. Nutr Cancer. 2015;67(8):1214–20. DOI: 10.1080/01635581.2015.1087042</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Nair P.P., Turjman N., Kessie G., Calkins B., Goodman G.T., Davidovitz H., et al. Diet, nutrition intake, and metabolism in populations at high and low risk for colon cancer. Dietary cholesterol, beta-sitosterol, and stigmasterol. Am J Clin Nutr. 1984;40(4 Suppl):927–30. DOI: 10.1093/ajcn/40.4.927</mixed-citation><mixed-citation xml:lang="en">Nair P.P., Turjman N., Kessie G., Calkins B., Goodman G.T., Davidovitz H., et al. Diet, nutrition intake, and metabolism in populations at high and low risk for colon cancer. Dietary cholesterol, beta-sitosterol, and stigmasterol. Am J Clin Nutr. 1984;40(4 Suppl):927–30. DOI: 10.1093/ajcn/40.4.927</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Jayaprakasha G.K., Mandadi K.K., Poulose S.M., Jadegoud Y., Nagana Gowda G.A., Patil B.S. Inhibition of colon cancer cell growth and antioxidant activity of bioactive compounds from Poncirus trifoliata (L.) Raf. Bioorg Med Chem. 2007;15(14):4923–32. DOI: 10.1016/j.bmc.2007.04.044</mixed-citation><mixed-citation xml:lang="en">Jayaprakasha G.K., Mandadi K.K., Poulose S.M., Jadegoud Y., Nagana Gowda G.A., Patil B.S. Inhibition of colon cancer cell growth and antioxidant activity of bioactive compounds from Poncirus trifoliata (L.) Raf. Bioorg Med Chem. 2007;15(14):4923–32. DOI: 10.1016/j.bmc.2007.04.044</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Macoska J.A. The use of beta-sitosterol for the treatment of prostate cancer and benign prostatic hyperplasia. Am J Clin Exp Urol. 2023;11(6):467–80. PMID: 38148931</mixed-citation><mixed-citation xml:lang="en">Macoska J.A. The use of beta-sitosterol for the treatment of prostate cancer and benign prostatic hyperplasia. Am J Clin Exp Urol. 2023;11(6):467–80. PMID: 38148931</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Kaighn M.E., Narayan K.S., Ohnuki Y., Lechner J.F., Jones L.W. Establishment and characterization of a human prostatic carcinoma cell line (PC-3). Invest Urol. 1979;17(1):16–23. PMID: 447482</mixed-citation><mixed-citation xml:lang="en">Kaighn M.E., Narayan K.S., Ohnuki Y., Lechner J.F., Jones L.W. Establishment and characterization of a human prostatic carcinoma cell line (PC-3). Invest Urol. 1979;17(1):16–23. PMID: 447482</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Awad A.B., Fink C.S., Williams H., Kim U. In vitro and in vivo (SCID mice) effects of phytosterols on the growth and dissemination of human prostate cancer PC-3 cells. Eur J Cancer Prev. 2001;10(6):507–13. DOI: 10.1097/00008469-200112000-00005</mixed-citation><mixed-citation xml:lang="en">Awad A.B., Fink C.S., Williams H., Kim U. In vitro and in vivo (SCID mice) effects of phytosterols on the growth and dissemination of human prostate cancer PC-3 cells. Eur J Cancer Prev. 2001;10(6):507–13. DOI: 10.1097/00008469-200112000-00005</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Awad A.B., Burr A.T., Fink C.S. Effect of resveratrol and beta-sitosterol in combination on reactive oxygen species and prostaglandin release by PC-3 cells. Prostaglandins Leukot Essent Fatty Acids. 2005;72(3):219– 26. DOI: 10.1016/j.plefa.2004.11.005</mixed-citation><mixed-citation xml:lang="en">Awad A.B., Burr A.T., Fink C.S. Effect of resveratrol and beta-sitosterol in combination on reactive oxygen species and prostaglandin release by PC-3 cells. Prostaglandins Leukot Essent Fatty Acids. 2005;72(3):219– 26. DOI: 10.1016/j.plefa.2004.11.005</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Segura R., Javierre C., Lizarraga M.A., Ros E. Other relevant components of nuts: phytosterols, folate and minerals. Br J Nutr. 2006;96(Suppl 2):S36–44. DOI: 10.1017/bjn20061862</mixed-citation><mixed-citation xml:lang="en">Segura R., Javierre C., Lizarraga M.A., Ros E. Other relevant components of nuts: phytosterols, folate and minerals. Br J Nutr. 2006;96(Suppl 2):S36–44. DOI: 10.1017/bjn20061862</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Calpe-Berdiel L., Escolà-Gil J.C., Blanco-Vaca F. New insights into the molecular actions of plant sterols and stanols in cholesterol metabolism. Atherosclerosis. 2009;203(1):18–31. DOI: 10.1016/j.atherosclerosis.2008.06.026</mixed-citation><mixed-citation xml:lang="en">Calpe-Berdiel L., Escolà-Gil J.C., Blanco-Vaca F. New insights into the molecular actions of plant sterols and stanols in cholesterol metabolism. Atherosclerosis. 2009;203(1):18–31. DOI: 10.1016/j.atherosclerosis.2008.06.026</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">O’Callaghan Y., Kenny O., O’Connell N.M., Maguire A.R., McCarthy F.O., O’Brien N.M. Synthesis and assessment of the relative toxicity of the oxidised derivatives of campesterol and dihydrobrassicasterol in U937 and HepG2 cells. Biochimie. 2013;95(3):496–503. DOI: 10.1016/j.biochi.2012.04.019</mixed-citation><mixed-citation xml:lang="en">O’Callaghan Y., Kenny O., O’Connell N.M., Maguire A.R., McCarthy F.O., O’Brien N.M. Synthesis and assessment of the relative toxicity of the oxidised derivatives of campesterol and dihydrobrassicasterol in U937 and HepG2 cells. Biochimie. 2013;95(3):496–503. DOI: 10.1016/j.biochi.2012.04.019</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Hsu H.F., Huang K.H., Lu K.J., Chiou S.J., Yen J.H., Chang C.C., et al. Typhonium blumei extract inhibits proliferation of human lung adenocarcinoma A549 cells via induction of cell cycle arrest and apoptosis. J Ethnopharmacol. 2011;135(2):492–500. DOI: 10.1016/j.jep.2011.03.048</mixed-citation><mixed-citation xml:lang="en">Hsu H.F., Huang K.H., Lu K.J., Chiou S.J., Yen J.H., Chang C.C., et al. Typhonium blumei extract inhibits proliferation of human lung adenocarcinoma A549 cells via induction of cell cycle arrest and apoptosis. J Ethnopharmacol. 2011;135(2):492–500. DOI: 10.1016/j.jep.2011.03.048</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Li Q., Jiang C., Zu Y., Song Z., Zhang B., Meng X., et al. SFE-CO2 extract from Typhonium giganteum Engl. tubers, induces apoptosis in human hepatoma SMMC-7721 cells involvement of a ROS-mediated mitochondrial pathway. Molecules. 2011;16(10):8228–42. DOI: 10.3390/molecules16108228</mixed-citation><mixed-citation xml:lang="en">Li Q., Jiang C., Zu Y., Song Z., Zhang B., Meng X., et al. SFE-CO2 extract from Typhonium giganteum Engl. tubers, induces apoptosis in human hepatoma SMMC-7721 cells involvement of a ROS-mediated mitochondrial pathway. Molecules. 2011;16(10):8228–42. DOI: 10.3390/molecules16108228</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Pinton P., Giorgi C., Siviero R., Zecchini E., Rizzuto R. Calcium and apoptosis: ER-mitochondria Ca2+ transfer in the control of apoptosis. Oncogene. 2008;27(50):6407–18. DOI: 10.1038/onc.2008.308</mixed-citation><mixed-citation xml:lang="en">Pinton P., Giorgi C., Siviero R., Zecchini E., Rizzuto R. Calcium and apoptosis: ER-mitochondria Ca2+ transfer in the control of apoptosis. Oncogene. 2008;27(50):6407–18. DOI: 10.1038/onc.2008.308</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Bae H., Park S., Yang C., Song G., Lim W. Disruption of endoplasmic reticulum and ROS production in human ovarian cancer by campesterol. Antioxidants. 2021;10:379. DOI: 10.3390/antiox10030379</mixed-citation><mixed-citation xml:lang="en">Bae H., Park S., Yang C., Song G., Lim W. Disruption of endoplasmic reticulum and ROS production in human ovarian cancer by campesterol. Antioxidants. 2021;10:379. DOI: 10.3390/antiox1003037</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>
