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    <identifier>10.57760/sciencedb.28670</identifier>
    <datestamp>2025-09-25T14:30:25Z</datestamp>
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  <dc:date>2025-09-25</dc:date>
  <dc:title>Hippo Pathway Deficiency in Gastric Pit Cells: A Spontaneous Mouse Model of Antral Carcinogenesis</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.28670</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Overview: Multi-omic profiling of a pit cell&amp;ndash;targeted double-knockout (DKO) mouse model of antral gastric carcinogenesis and wild-type (WT) controls, all from gastric antrum tissue. Modalities include single-cell RNA sequencing (scRNA-seq), spatial transcriptomics, bulk proteomics, and untargeted metabolomics with age-matched designs.scRNA-seq: DKO (12 mice at 3, 6, 9, and 12 months; three per age) pooled within age to generate four DKO libraries; WT tissues from four mice (one per age) were pooled across ages to produce a single control library.Spatial transcriptomics: Four samples from the contralateral antrum of the scRNA-seq cohort: one DKO and one age-matched WT at 6 months, and one DKO and one WT at 12 months.Proteomics: Twelve antral tissues across four groups (DKO4, DKO8, WT4, WT8; n=3 per group) for quantitative protein profiling.Metabolomics: Thirty-two antral tissues across the same four groups (n=8 per group). Untargeted acquisition was performed in both positive and negative ion modes.</dc:description>
  <dc:subject>Hippo pathway; mouse model; gastric cancer; scRNA-seq; Spatial transcriptomics</dc:subject>
  <dc:creator>Wangyu Cai</dc:creator>
  <dc:creator>Wen Xie</dc:creator>
  <dc:rights>RESTRICTED</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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