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      <ref-type name="Journal Article">17</ref-type>
      <contributors>
        <authors>
          <author>Aiqin Liu</author>
          <author>Bing Yan</author>
          <author>Richeng Jiang</author>
        </authors>
      </contributors>
      <titles>
        <title>MULBERROSIDE A EXTRACT ENHANCES THE ANTITUMOR EFFICACY OF PACLITAXEL BY INHIBITING THE HIF-1Α/SHH SIGNALING PATHWAY IN LEWIS LUNG CARCINOMA-BEARING MICE</title>
        <secondary-title>Journal of Animal and Plant Sciences</secondary-title>
        <alt-title>JAPS</alt-title>
      </titles>
      <dates><year>2026</year><pub-dates><date>2026</date></pub-dates></dates>
      <volume>36</volume>
      <number>6</number>
      <isbn>1018-7081</isbn>
      <electronic-resource-num>https://doi.org/10.36899/JAPS.2026.6.0149</electronic-resource-num>
      <abstract>&lt;p style=&quot;text-align: justify;&quot;&gt;The present work set out to determine whether Mulberroside A (MA) extract could boost the antitumor efficacy of paclitaxel (PTX) in Lewis lung carcinoma (LLC)-bearing mice through modulation of the HIF-1&amp;alpha;/SHH signaling pathway. LLC-bearing C57BL/6 mice were randomized into control, model, PTX, MA, PTX+MA, PTX+MA+HIF-1&amp;alpha; inhibitor (YC-1) and PTX+MA+SHH inhibitor (Cyclopamine) groups. Tumor growth, apoptosis (TUNEL), microvascular density (MVD and CD31 staining), and histopathology (H&amp;amp;E) were assessed. Expression of HIF-1&amp;alpha;/SHH pathway components and downstream targets (VEGF, Bcl-2 and caspase-3) was measured by qPCR, and Western blot.&amp;nbsp;&amp;nbsp;PTX+MA synergistically inhibited tumor growth and reduced MVD versus PTX alone (&lt;em&gt;P&lt;/em&gt;&amp;le;0.05), while a higher level of apoptotic cells was observed (&lt;em&gt;P&lt;/em&gt;&amp;le;0.05). This was accompanied by downregulation of HIF-1&amp;alpha;, SHH, SMO, GLI1, VEGF, and Bcl-2, and upregulation of caspase-3 (&lt;em&gt;P&lt;/em&gt;&amp;le;0.05). Addition of HIF-1&amp;alpha; or SHH inhibitors partially reversed these effects, confirming pathway involvement. MA enhances PTX antitumor efficacy in LLC-bearing mice by suppressing the HIF-1&amp;alpha;/SHH axis, thereby inhibiting angiogenesis and promoting apoptosis. This combination may represent a potential strategy to improve chemotherapy efficacy in lung cancer.&lt;/p&gt;</abstract>
      <keywords><keyword>Mulberroside A extract; HIF-1α/SHH pathway; lung cancer; tumor-bearing mice; paclitaxel</keyword></keywords>
      <publisher>Pakistan Agricultural Scientists Forum</publisher>
      <urls><related-urls><url>https://thejaps.org.pk/AbstractView.aspx?mid=2025-JAPS-1366</url></related-urls></urls>
    </record>
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