﻿<?xml version="1.0" encoding="UTF-8"?>
<ArticleSet>
  <Article>
    <Journal>
      <PublisherName>Shahrekord University of Medical Sciences</PublisherName>
      <JournalTitle>Journal of Herbmed Pharmacology</JournalTitle>
      <Issn>2345-5004</Issn>
      <Volume>4</Volume>
      <Issue>2</Issue>
      <PubDate PubStatus="ppublish">
        <Year>2015</Year>
        <Month>04</Month>
        <DAY>01</DAY>
      </PubDate>
    </Journal>
    <ArticleTitle>Cytotoxic activities of Euphorbia kopetdaghi against OVCAR-3 and EJ-138 cell lines</ArticleTitle>
    <FirstPage>49</FirstPage>
    <LastPage>52</LastPage>
    <Language>EN</Language>
    <AuthorList>
      <Author>
        <FirstName>Mahmoud</FirstName>
        <LastName>Aghaei</LastName>
      </Author>
      <Author>
        <FirstName>Mustafa</FirstName>
        <LastName>Ghanadian</LastName>
      </Author>
      <Author>
        <FirstName>Farough</FirstName>
        <LastName>Faez</LastName>
      </Author>
      <Author>
        <FirstName>Ebrahim</FirstName>
        <LastName>Esfandiary</LastName>
      </Author>
    </AuthorList>
    <PublicationType>Journal Article</PublicationType>
    <ArticleIdList>
      <ArticleId IdType="doi">
      </ArticleId>
    </ArticleIdList>
    <History>
    </History>
    <Abstract>Introduction: Over the centuries, the genus Euphorbia was known to be toxic to humans and animals. Recently, in a primary study significant suppressive activity against phytohemagglutinin activated T-cell proliferation has been reported from this plant. Therefore, this study was designed to evaluate the cytotoxic effects of different parts of E. kopetdaghi against cancer cell lines. Methods: Filtration and in vacuo concentration resulted in a green gum which was subjected on silica gel CC (hexane/Acetone, 0 →50) to several fractions: F1-F8. The inhibitory effects of obtained fractions with 5, 50, and 500 μg/ml concentrations were evaluated on proliferation and viability of cancer cells (OVCAR and EJ-138) in 48 hours treatment. Finally, cell viability was determined at a wavelength of 570 by 3-4,5-dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) method. Results: Based on studies of microscopic observation and viability testing, F1, F2, F4, F5, F6, and F7 showed significant cytotoxic effect at concentration of 50 and 500 μg/ml against EJ-138 and OVCAR-3 cell lines. These fractions inhibited growth of EJ-138 and OVCAR-3 cells in a concentration-dependent manner. Fraction of F8 induced tumor promotion significantly in EJ-138 and OVCAR-3 cells, respectively. Conclusion: Due to the inhibitory properties of E. kopetdaghi extract and its fractions on cancer cells of OVCAR3 and EJ-13, isolation, purification and identification of compounds presented in the fractions possessing cytotoxic effects are recommended which were the area of our future research.</Abstract>
    <ObjectList>
      <Object Type="keyword">
        <Param Name="value">Euphorbiaceae</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">Euphorbia kopetdaghi</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">cytotoxicity</Param>
      </Object>
      <Object Type="keyword">
        <Param Name="value">OVCAR</Param>
      </Object>
    </ObjectList>
  </Article>
</ArticleSet>