{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,12]],"date-time":"2026-10-12T18:50:09Z","timestamp":1791831009866,"version":"4.3.4"},"reference-count":21,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"1","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2017,1]]},"abstract":"<jats:sec>\n                    <jats:title>Background:<\/jats:title>\n                    <jats:p>\n                      Cancer is a term for a large group of different diseases, all involving uncontrolled cell growth. Many of\n                      <jats:italic toggle=\"yes\">Euphorbiaceae<\/jats:italic>\n                      plants have been traditionally used for the treatment of ulcers, tumors, warts, and other diseases. In addition, in the last decade, there are studies showing cytotoxic effects of different species of\n                      <jats:italic toggle=\"yes\">Euphorbia<\/jats:italic>\n                      on tumor cell lines. In this study, we attempted to determine if\n                      <jats:italic toggle=\"yes\">Euphorbia turcomanica<\/jats:italic>\n                      possess any cytotoxic activity.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Materials and Methods:<\/jats:title>\n                    <jats:p>Solvents extracted the plant powder with various polarities by a maceration method, and qualitative phytochemical analyzes were carried out on them to identify the constituents. On the other hand, the possible cytotoxicity of different extracts on Hela and HT-29 tumor cells was measured by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay and 50% reduction in cell survival was considered as a cytotoxic effect. Analyze of variance followed by Student-Newman-Keuls test was used to see the differences among the groups.<\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Results:<\/jats:title>\n                    <jats:p>\n                      Phytochemical analysis of\n                      <jats:italic toggle=\"yes\">E. turcomanica<\/jats:italic>\n                      showed the presence of flavonoid, alkaloid, anthraquinone and tannin in plant aerial parts. Methanol-water, acetone, dichloromethane, methanol, and heptane extracts of\n                      <jats:italic toggle=\"yes\">E. turcomanica<\/jats:italic>\n                      significantly reduced viability of Hela cells (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt; 0.05) with inhibitory concentration 50% (IC\n                      <jats:sub>50<\/jats:sub>\n                      ) of 50, 90, 230, 420, and 450 \u03bcg\/ml, respectively. While methanol-water, dichloromethane, methanol, ethyl acetate, and heptane extracts were cytotoxic with IC\n                      <jats:sub>50<\/jats:sub>\n                      of 43, 115, 125, 250, and 390 \u03bcg\/ml, respectively (\n                      <jats:italic toggle=\"yes\">P<\/jats:italic>\n                      &lt; 0.05), on HT-29 cells.\n                    <\/jats:p>\n                  <\/jats:sec>\n                  <jats:sec>\n                    <jats:title>Conclusion:<\/jats:title>\n                    <jats:p>\n                      It can be concluded that\n                      <jats:italic toggle=\"yes\">E. turcomanica<\/jats:italic>\n                      is a good candidate for further study toward cytotoxic agents.\n                    <\/jats:p>\n                  <\/jats:sec>","DOI":"10.4103\/2277-9175.192734","type":"journal-article","created":{"date-parts":[[2016,10,20]],"date-time":"2016-10-20T06:35:55Z","timestamp":1476945355000},"update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":13,"title":["Phytochemical Screening and Cytotoxic Evaluation of Euphorbia turcomanica on Hela and HT-29 Tumor Cell Lines"],"prefix":"10.4103","volume":"6","author":[{"given":"Mehdi","family":"Aliomrani","sequence":"first","affiliation":[{"name":"From the Department of Toxicology and Pharmacology, School of Pharmacy, Tehran University of Medical Sciences, Tehran, Iran"},{"name":"Department of Pharmaceutical Biotechnology, School of Pharmacy and Pharmaceutical Sciences, Isfahan University of Medical Sciences, Isfahan, Iran"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Abbas","family":"Jafarian","sequence":"additional","affiliation":[{"name":"Department of Pharmaceutical Biotechnology, 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