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    <journal-meta>
      <journal-id journal-id-type="nlm-ta">Avicenna J Med Biotech</journal-id>
      <journal-id journal-id-type="publisher-id">arij002</journal-id>
      <journal-title-group>
        <journal-title>Avicenna Journal of Medical Biotechnology</journal-title>
      </journal-title-group>
      <issn pub-type="ppub">2008-2835</issn>
      <issn pub-type="epub">2008-4625</issn>
      <publisher>
        <publisher-name>Avicenna Research Institute</publisher-name>
      </publisher>
    </journal-meta>

    <article-meta>
      <article-id pub-id-type="publisher-id">ajmb230</article-id>
      <article-id pub-id-type="doi"></article-id>
      <article-id pub-id-type="pmid"></article-id>
      <article-categories>
        <subj-group subj-group-type="heading">
             <subject></subject> 
        </subj-group>
        <subj-group>
            <subject></subject>
        </subj-group> 
      </article-categories>
      <title-group>
        <article-title>Evaluation of the Anti-proliferative Effects of &lt;i&gt;Ophiocoma erinaceus&lt;/i&gt; Methanol Extract Against Human Cervical Cancer Cells</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Baharara</surname><given-names>Javad</given-names></name></contrib><aff>Monoclonal Antibody Research Center, Avicenna Research Institute, ACECR, Tehran, Iran</aff></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Amini</surname><given-names>Elaheh</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Namvar</surname><given-names>Farideh</given-names></name></contrib><aff>Department of Radiation Oncology, Shohada Tajrish Hospital, Shahid Beheshti University of Medical Science, Tehran, Iran</aff></contrib-group>
      <pub-date pub-type="ppub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <pub-date pub-type="epub">
        <day></day>
        <month></month>
        <year></year>
      </pub-date>
      <volume>8</volume>
      <issue>1</issue>
      <fpage>29</fpage>
      <lpage>35</lpage>
      <history>
        <date date-type="received">
          <day>11</day>
          <month>7</month>
          <year>2015</year>
        </date>
        <date date-type="accepted">
          <day>15</day>
          <month>10</month>
          <year>2015</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p&gt;Background: Marine organisms provide appreciable source of novel bioactive compounds with pharmacological potential. There is little information in correlation with anti-cancer activities of brittle star. In the present study, anti-neoplastic efficacy of &lt;em&gt;Ophiocoma erinaceus&lt;/em&gt; methanol extract against human cervical cancer cells was investigated.&lt;br /&gt;
Methods: The HeLa cells were cultured and exposed to brittle star methanol extract for 24 and 48 &lt;em&gt;hr&lt;/em&gt;. The anti-proliferative properties were examined by MTT assay and the type of cell death induced was evaluated through morphological changes, flow cytometry, Annexin kit and caspase assay. To assess the anti-metastatic activity, wound healing assay was conducted and photographs were taken from the scratched areas. Further, to understand molecular mechanism of cell apoptosis, the expression of Bax was evaluated.&lt;br /&gt;
Results: The morphological analysis and MTT assay exhibited that the brittle star methanol extract can exert dose dependent inhibitory effect on cells viability (IC&lt;sub&gt;50&lt;/sub&gt;, 50 &lt;em&gt;&amp;mu;g/ml&lt;/em&gt;). Flow cytometry and fluorescence microscopy demonstrated increment of sub-G1 peak, early and late apoptosis in HeLa treated cells. Wound healing migration assay showed that brittle star extract has anti-neoplastic efficacy by inhibiting cell migration. Caspase assay and RT-PCR analysis revealed that brittle star methanol extract induced caspase dependent apoptosis in HeLa cells through up-regulation of caspase-3 followed by up-regulation of Bax gene which is a hallmark of intrinsic pathway recruitment.&lt;br /&gt;
Conclusion: These results represented further insights into the chemopreventive potential of brittle star as a valuable source of unknown therapeutic agents against human cervical cancer.&lt;/p&gt;

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      </abstract>
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