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<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="research-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Acta Naturae</journal-id><journal-title-group><journal-title xml:lang="en">Acta Naturae</journal-title><trans-title-group xml:lang="ru"><trans-title>Acta Naturae</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2075-8251</issn><publisher><publisher-name xml:lang="en">Acta Naturae Ltd</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">10310</article-id><article-id pub-id-type="doi">10.32607/20758251-2019-11-1-81-90</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Research Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Экспериментальные статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Research Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Mauritian Endemic Medicinal Plant Extracts Induce G2/M Phase Cell Cycle Arrest and Growth Inhibition of Oesophageal Squamous Cell Carcinoma in Vitro</article-title><trans-title-group xml:lang="ru"><trans-title>Mauritian Endemic Medicinal Plant Extracts Induce G2/M Phase Cell Cycle Arrest and Growth Inhibition of Oesophageal Squamous Cell Carcinoma in Vitro</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name><surname>Rummun</surname><given-names>N.</given-names></name><address><country country="MU">Mauritius</country></address><email>v.neergheen@uom.ac.mu</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff7"/></contrib><contrib contrib-type="author"><name><surname>Hughes</surname><given-names>R. E.</given-names></name><address><country country="GB">United Kingdom</country></address><email>v.neergheen@uom.ac.mu</email></contrib><contrib contrib-type="author"><name><surname>Beesoo</surname><given-names>R.</given-names></name><address><country country="MU">Mauritius</country></address><email>v.neergheen@uom.ac.mu</email><xref ref-type="aff" rid="aff9"/><xref ref-type="aff" rid="aff7"/><xref ref-type="aff" rid="aff6"/><xref ref-type="aff" rid="aff9"/></contrib><contrib contrib-type="author"><name><surname>Li</surname><given-names>W. W.</given-names></name><address><country country="GB">United Kingdom</country></address><email>v.neergheen@uom.ac.mu</email></contrib><contrib contrib-type="author"><name><surname>Aldulaimi</surname><given-names>O.</given-names></name><address><country country="GB">United Kingdom</country></address><email>v.neergheen@uom.ac.mu</email></contrib><contrib contrib-type="author"><name><surname>Macleod</surname><given-names>K. G.</given-names></name><address><country country="GB">United Kingdom</country></address><email>v.neergheen@uom.ac.mu</email><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name><surname>Bahorun</surname><given-names>T.</given-names></name><address><country country="MU">Mauritius</country></address><email>v.neergheen@uom.ac.mu</email><xref ref-type="aff" rid="aff7"/></contrib><contrib contrib-type="author"><name><surname>Carragher</surname><given-names>N. O.</given-names></name><address><country country="GB">United Kingdom</country></address><email>N.Carragher@ed.ac.uk</email><xref ref-type="aff" rid="aff6"/></contrib><contrib contrib-type="author"><name><surname>Kagansky</surname><given-names>A.</given-names></name><address><country country="GB">United Kingdom</country></address><email>kagasha@yahoo.com</email><xref ref-type="aff" rid="aff6"/><xref ref-type="aff" rid="aff8"/></contrib><contrib contrib-type="author"><name><surname>Neergheen-Bhujun</surname><given-names>V. S.</given-names></name><address><country country="MU">Mauritius</country></address><email>v.neergheen@uom.ac.mu</email><xref ref-type="aff" rid="aff9"/><xref ref-type="aff" rid="aff7"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">University of Mauritius</institution></aff><aff><institution xml:lang="ru"></institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">ANDI Centre of Excellence for Biomedical and Biomaterials Research</institution></aff><aff><institution xml:lang="ru"></institution></aff></aff-alternatives><aff-alternatives id="aff3"><aff><institution xml:lang="en">Institute for Science and Technology in Medicine</institution></aff><aff><institution xml:lang="ru"></institution></aff></aff-alternatives><aff-alternatives id="aff4"><aff><institution xml:lang="en">Cancer Research UK Edinburgh Centre, University of Edinburgh</institution></aff><aff><institution xml:lang="ru"></institution></aff></aff-alternatives><aff-alternatives id="aff5"><aff><institution xml:lang="en">University of Edinburgh</institution></aff><aff><institution xml:lang="ru"></institution></aff></aff-alternatives><aff id="aff6"><institution>University of Edinburgh</institution></aff><aff id="aff7"><institution>ANDI Centre of Excellence for Biomedical and Biomaterials Research</institution></aff><aff id="aff8"><institution>Far Eastern Federal University</institution></aff><aff id="aff9"><institution>University of Mauritius</institution></aff><pub-date date-type="pub" iso-8601-date="2019-03-15" publication-format="electronic"><day>15</day><month>03</month><year>2019</year></pub-date><volume>11</volume><issue>1</issue><issue-title xml:lang="en">VOL 11, NO1 (2019)</issue-title><issue-title xml:lang="ru">ТОМ 11, №1 (2019)</issue-title><fpage>81</fpage><lpage>90</lpage><history><date date-type="received" iso-8601-date="2020-01-17"><day>17</day><month>01</month><year>2020</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2019, Rummun N., Hughes R.E., Beesoo R., Li W.W., Aldulaimi O., Macleod K.G., Bahorun T., Carragher N.O., Kagansky A., Neergheen-Bhujun V.S.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2019, Rummun N., Hughes R.E., Beesoo R., Li W.W., Aldulaimi O., Macleod K.G., Bahorun T., Carragher N.O., Kagansky A., Neergheen-Bhujun V.S.</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="en">Rummun N., Hughes R.E., Beesoo R., Li W.W., Aldulaimi O., Macleod K.G., Bahorun T., Carragher N.O., Kagansky A., Neergheen-Bhujun V.S.</copyright-holder><copyright-holder xml:lang="ru">Rummun N., Hughes R.E., Beesoo R., Li W.W., Aldulaimi O., Macleod K.G., Bahorun T., Carragher N.O., Kagansky A., Neergheen-Bhujun V.S.</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://actanaturae.ru/2075-8251/article/view/10310">https://actanaturae.ru/2075-8251/article/view/10310</self-uri><abstract xml:lang="en"><p>Terrestrial plants have contributed massively to the development of modern oncologic drugs. Despite the wide acceptance of Mauritian endemic flowering plants in traditional medicine, scientific evidence of their chemotherapeutic potential is lacking. This study aimed to evaluate the in vitro tumor cytotoxicity of leaf extracts from five Mauritian endemic medicinal plants, namely Acalypha integrifolia Willd (Euphorbiaceae), Labourdonnaisia glauca Bojer (Sapotaceae), Dombeya acutangula Cav. subsp. rosea Friedmann (Malvaceae), Gaertnera psychotrioides (DC.) Baker (Rubiaceae), and Eugenia tinifolia Lam (Myrtaceae).<ext-link ext-link-type="uri" xlink:href="https://www.yogatrail.com/blog/wp-includes/random_compat/rolex-oyster-perpetual-day-date-real-or-fake.html">rolex oyster perpetual day date real or fake</ext-link> The cytotoxicities of the extracts were determined against six human cancer cell lines, including cervical adenocarcinoma, colorectal carcinoma, oesophageal adenocarcinoma, and oesophageal squamous cell carcinoma. The potent extracts were further investigated using cell cycle analysis and reverse phase protein array (RPPA) analysis. The antioxidant properties and polyphenolic profile of the potent extracts were also evaluated. Gas chromatography mass spectrometry (GC-MS) analyses revealed the presence of (+)-catechin and gallocatechin in E. tinifolia and L. glauca, while gallic acid was detected in A. integrifolia. L. glauca, A. integrifolia, and E. tinifolia were highly selective towards human oesophageal squamous cell carcinoma (KYSE-30) cells. L. glauca and E. tinifolia arrested KYSE- 30 cells in the G2/M phase, in a concentration-dependent manner. RPPA analysis indicated <ext-link ext-link-type="uri" xlink:href="http://www.danek.cz/common/ckeditor/plugins/showblocks/images/how-to-know-if-rolex-fake.html">rolex fake</ext-link> that the extracts may partly exert their tumor growth-inhibitory activity by upregulating the intracellular level of 5′AMP-activated kinase (AMPK). The findings highlight the potent antiproliferative activity of three Mauritian endemic leaf extracts against oesophageal squamous c<ext-link ext-link-type="uri" xlink:href="https://www.sendets.fr/admin/highslide/graphics/outlines/cheap-replica-luxury-watches.html">cheap replica luxury watches</ext-link> ell carcinoma and calls for further investigation into their chemotherapeutic application.</p></abstract><trans-abstract xml:lang="ru"><p>Terrestrial plants have contributed massively to the development of modern oncologic drugs. Despite the wide acceptance of Mauritian endemic flowering plants in traditional medicine, scientific evidence of their chemotherapeutic potential is lacking. This study aimed to evaluate the in vitro tumor cytotoxicity of leaf extracts from five Mauritian endemic medicinal plants, namely Acalypha integrifolia Willd (Euphorbiaceae), Labourdonnaisia glauca Bojer (Sapotaceae), Dombeya acutangula Cav. subsp. rosea Friedmann (Malvaceae), Gaertnera psychotrioides (DC.) Baker (Rubiaceae), and Eugenia tinifolia Lam (Myrtaceae). The cytotoxicities of the extracts were determined against six human cancer cell lines, including cervical adenocarcinoma, colorectal carcinoma, oesophageal adenocarcinoma, and oesophageal squamous cell carcinoma. The potent extracts were further investigated using cell cycle analysis and reverse phase protein array (RPPA) analysis. The antioxidant properties and polyphenolic profile of the potent extracts were also evaluated. Gas chromatography mass spectrometry (GC-MS) analyses revealed the presence of (+)-catechin and gallocatechin in E. tinifolia and L. glauca, while gallic acid was detected in A. integrifolia. L. glauca, A. integrifolia, and E. tinifolia were highly selective towards human oesophageal squamous cell carcinoma (KYSE-30) cells. L. glauca and E. tinifolia arrested KYSE- 30 cells in the G2/M phase, in a concentration-dependent manner. RPPA analysis indicated that the extracts may partly exert their tumor growth-inhibitory activity by upregulating the intracellular level of 5′AMP-activated kinase (AMPK). The findings highlight the potent antiproliferative activity of three Mauritian endemic leaf extracts against oesophageal squamous cell carcinoma and calls for further investigation into their chemotherapeutic application.</p></trans-abstract><kwd-group xml:lang="en"><kwd>Mauritian endemic</kwd><kwd>medicinal plant</kwd><kwd>oesophageal carcinoma</kwd><kwd>tumor cytotoxicity</kwd><kwd>AMPK</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>[1] Pennathur A., Gibson M.K., Jobe B.A., Luketich J.D. // Lancet. 2013, V.381, №9864, P.400-412</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>[2] Napier K.J. // World J. Gastrointest. 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