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    <identifier>10.57760/sciencedb.22961</identifier>
    <datestamp>2025-04-07T18:12:54Z</datestamp>
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<oai_dc:dc xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:date>2025-04-07</dc:date>
  <dc:title>The antitumor efficacy of Ganoderma lucidum spore oil in hepatoma H22-bearing mice depends on modulating immunity and inhibiting eicosanoid metabolism pathway in tumor cells</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.22961</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Ganoderma lucidum&amp;nbsp;spore oil&amp;nbsp;(GLSO) is a well-known dietary supplement that is beneficial for immuno-enhancement. Based on the close correlation between tumor occurrence and immunity. The immuno-enhancement&amp;nbsp;ability of GLSO in hepatoma H22-bearing mice was investigated in this study, and our work aimed to reveal the potential mechanisms of the antitumor efficacy&amp;nbsp;of GLSO. The&amp;nbsp;GLSO&amp;nbsp;components were identified via UHPLC-Q-Orbitrap HRMS. A H22 cell subcutaneously transplanted tumor mouse model was constructed, and GLSO was preadministered. The antitumor efficacy&amp;nbsp;of GLSO in hepatoma H22-bearing mice was evaluated according to tumor size, tumor growth curves, tumor inhibition rates and Ki67 expression level. T and B lymphocyte proliferation, delayed hypersensitivity, NK cell killing activity, macrophage phagocytotic activity, cytokine levels and CD69 molecule expression were detected to estimate immune function. Flow cytometry and Pro-DIA quantitative proteomics analysis were performed to investigate the potential mechanism of GLSO in tumor inhibition, which was verified by WB and RT-PCR. Thirty-eight&amp;nbsp;compounds&amp;nbsp;including triterpenoids, fatty acids and&amp;nbsp;esters, were identified from GLSO.&amp;nbsp;GLSO treatment prevented tumor occurrence and inhibited&amp;nbsp;tumor growth&amp;nbsp;because of the smaller initial and final tumor volumes and lower Ki67 expression. Treatment with GLSO promoted a&amp;nbsp;strong immune response in hepatoma H22-bearing mice&amp;nbsp;and improved tumor&amp;nbsp;immune microenvironment. Proteomics analysis showed that GLSO inhibited eicosanoid metabolism&amp;nbsp;pathway, WB and RT-PCR re-check these results. In conclusion, these findings support that GLSO prevents the occurrence of tumor depending on its immunomodulatory effects&amp;nbsp;and we first report&amp;nbsp;that GLSO restricts&amp;nbsp;tumor growth&amp;nbsp;by inhibiting eicosanoid metabolism&amp;nbsp;pathway.</dc:description>
  <dc:subject>Ganoderma lucidum spore oil; antitumor efficacy; immune enhancement; eicosanoid metabolism pathway; hepatoma H22-bearing mice</dc:subject>
  <dc:creator>Xueqian XIE</dc:creator>
  <dc:creator>Hongxu CHEN</dc:creator>
  <dc:creator>Shuiling CAO</dc:creator>
  <dc:creator>Rui XU</dc:creator>
  <dc:creator>Yanping CAI</dc:creator>
  <dc:creator>Bo XU</dc:creator>
  <dc:creator>Yunliang CHEN</dc:creator>
  <dc:creator>Kehan CHEN</dc:creator>
  <dc:creator>Wentao WEN</dc:creator>
  <dc:creator>Meng ZHAO</dc:creator>
  <dc:creator>Xuezhou KE</dc:creator>
  <dc:creator>Qi YI</dc:creator>
  <dc:creator>Chunjing LI</dc:creator>
  <dc:creator>Qing WANG</dc:creator>
  <dc:creator>Lian ZHOU</dc:creator>
  <dc:creator>Xia LUO</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-sa/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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