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    <responseDate>2026-10-12T11:11:37Z</responseDate>
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    <identifier>10.57760/sciencedb.j00217.11626</identifier>
    <datestamp>2026-01-22T11:16:28Z</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>2026-01-22</dc:date>
  <dc:title>Investigation of the Anti-Lung Cancer Activity and Mechanism of Umbilical Cord Blood Stem Cell-Derived NK Cell Exosomes</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.j00217.11626</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Objective In order to determine the therapeutic efficacy and mechanism of action of natural killer cell-based exosomes from umbilical cord blood stem cells (UCB-NK-EXO) in a lung cancer model.Methods Cultured umbilical cord blood mononuclear cells (CBMCs) followed by IL-21 culture system to expand NK cells. All exosomes were isolated as well as obtained from the collected cell culture supernatant. The proliferation and apoptosis caused by UCB-NK-EXO to A549 lung cancer cells are observed by the CCK-8test and flow cytometry. Uptake by cells after exosome treatment was checked with confocal microscopy. A549 xenograft tumors were made in nude mice, and UCB-NK-EXO was given through the tail vein. The tumor growth happens and the liver &amp;amp; kidney in serum was checked for functions tests. I used western blot methodology to find out if there was a related-apoptosis signaling molecule in the tumor squads.Results UCB-NK-EXO greatly inhibited the proliferation of A549 cells (P &amp;lt;0.01), and promoted the apoptosis of the cells (P&amp;lt;0.001). It was also successfully internalized by the cells. The UCB-NK-EXO group had a much stronger anti-tumor effect than the DOX group in the in vivo experiments and also had a better effect on survival time p&amp;lt;0.001. UCB-NK-EXO treatment has no bodyweight loss and no hepatorenal toxicity of above Western blot results show cytotoxic protein like Granzyme B &amp;amp; Perforin exist in UCB-NK-EXO and Tumor tissue has very high expression of Apoptotic proteins like Caspase related proteins.Conclusion UCB-NK-EXO effectively inhibits the growth of A549 lung cancer both in vitro and in vivo. The mechanism involves the delivery of cytotoxic proteins to tumor cells, activation of the Caspase-dependent apoptosis pathway, and subsequent induction of tumor cell apoptosis. UCB-NK-EXO demonstrates superior antitumor efficacy and a more favorable safety profile compared to the conventional chemotherapeutic agent doxorubicin.</dc:description>
  <dc:subject>Natural killer cells; Exosomes; Tumor; Umbilical cord blood stem cells</dc:subject>
  <dc:creator>Jingjing.Wang</dc:creator>
  <dc:creator>Cailing.Tong</dc:creator>
  <dc:creator>Taoling.Yan</dc:creator>
  <dc:creator>Zhanqing.Li</dc:creator>
  <dc:creator>Xuemei.Wu</dc:creator>
  <dc:creator>Anyun.Wu</dc:creator>
  <dc:creator>Yufei.Long</dc:creator>
  <dc:creator>Zhenting.Lin</dc:creator>
  <dc:creator>Zhongquan.Qi</dc:creator>
  <dc:creator>Tianshu.Lan</dc:creator>
  <dc:rights>EMBARGO</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by-nc-nd/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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