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    <responseDate>2026-10-14T17:35:14Z</responseDate>
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    <identifier>10.57760/sciencedb.36071</identifier>
    <datestamp>2026-04-30T08:38:00Z</datestamp>
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  <dc:date>2026-04-30</dc:date>
  <dc:title>Quantitative secretome atlas of soluble E-cadherin-driven vascular leakage in the lung pre-metastatic niche of salivary adenoid cystic carcinoma</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.36071</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>This data set reports the comprehensive, label-free quantitative proteomic profile of conditioned media from high-metastatic (SACC-LM) versus low-metastatic (SACC-83) salivary adenoid cystic carcinoma cells. LC-MS/MS analysis identified and quantified 5,342 proteins (FDR &amp;le; 1 % at PSM, protein level), of which 1,847 were significantly differentially secreted (&amp;ge; 2-fold change, p &amp;le; 0.05). Bioinformatic enrichment highlighted over-representation of cell-adhesion molecules, serine hydrolases and apical-junction components, with soluble E-cadherin (sE-cad/CDH1) displaying the strongest up-regulation (22-fold) in the metastatic secretome. The inventory provides a resource for investigating tumour-derived factors that destabilise endothelial tight-junctions via the Rac2/LIMK/cofilin-1 axis and offers candidate biomarkers for monitoring or targeting the lung pre-metastatic niche in SACC.</dc:description>
  <dc:subject>E-cadherin; metastasis; Salivary adenoid cystic carcinoma</dc:subject>
  <dc:creator>Zhou Jinwen</dc:creator>
  <dc:creator>You Quan</dc:creator>
  <dc:creator>Jiang Jian</dc:creator>
  <dc:creator>Guo Tao</dc:creator>
  <dc:creator>Kong Jing</dc:creator>
  <dc:rights>RESTRICTED</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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