

<!DOCTYPE article PUBLIC "-//NLM//DTD Journal Publishing DTD v3.0 20080202//EN" "journalpublishing3.dtd">
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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">ajmb70637</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>Curcuma xanthorrhiza Extract Modulates CASP3 and TIMP1 Expression and  Regulates 8-OHdG, Collagen, and Protein Levels in UV-Induced BJ Cells</article-title>
      </title-group>
        <contrib-group><contrib contrib-type="author"><name><surname>Widowati</surname><given-names>Wahyu</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Hidayat</surname><given-names>Meilinah</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Tjokropranoto</surname><given-names>Rita</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Nur Triharsiwi </surname><given-names>Dwi</given-names></name></contrib></contrib-group><contrib-group><contrib contrib-type="author"><name><surname>Sari Widya Kusuma</surname><given-names>Hanna</given-names></name></contrib></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>18</volume>
      <issue>1</issue>
      <fpage>48</fpage>
      <lpage>54</lpage>
      <history>
        <date date-type="received">
          <day>4</day>
          <month>7</month>
          <year>2025</year>
        </date>
        <date date-type="accepted">
          <day>8</day>
          <month>10</month>
          <year>2025</year>
        </date>
      </history>
      <abstract>
      <p>
      &lt;p&gt;Background: Ultraviolet (UV) radiation poses a significant health risk, particularly in high-exposure regions including Indonesia, contributing to more than 1.5 million UV-related Disability-Adjusted Life Years (DALYs) globally due to its involvement in photoaging, skin cancers, and chronic inflammation. This study aimed to evaluate the Curcuma xanthorrhiza extract (CXE) mitigating effects against UV-induced damage in human dermal fibroblasts (BJ cells) by assessing gene expression, protein integrity, DNA damage, and collagen levels. Methods: BJ fibroblasts were irradiated to UV radiation and given CXE at 3.13&amp;ndash;12.5 &amp;micro;g/ml concentrations. TIMP1 and CASP3 gene expression were analyzed via qRT-PCR, while total protein, 8-hydroxy-2&amp;prime;-deoxyguanosine (8-OHdG), and collagen content were measured using ELISA. Results: CXE treatment significantly upregulated TIMP1 and downregulated CASP3 expression in a concentration-dependent manner, with the strongest effects showed at 12.5 &amp;micro;g/ml (p&amp;lt;0.05). At the same concentration, CXE significantly restored total protein levels, reduced 8-OHdG accumulation, and preserved collagen content compared with the UV-induced control (p&amp;lt;0.05). Conclusion: These findings suggest CXE exerts reparative effects against UV-induced photoaging through antioxidant, anti-apoptotic, and Extracellular Matrix (ECM) preserving mechanisms, supporting its potential as a botanical anti-aging therapy.&lt;/p&gt;

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      </abstract>
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