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        <identifier>oai:figshare.com:article/33771097</identifier>
        <datestamp>2026-09-15T04:30:04Z</datestamp>
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          <dc:title>Supplementary file 1_GATA2-driven ZNF486-JAM2 activation collaboratively counteracts epithelial-mesenchymal transition and in vitro invasion in endometrial cancer.docx</dc:title>
          <dc:creator>Xing Fan (88299)</dc:creator>
          <dc:creator>Zhengjiao Tong (24558813)</dc:creator>
          <dc:creator>Yingxia Ou (24912052)</dc:creator>
          <dc:creator>Xiaoli Wang (46677)</dc:creator>
          <dc:creator>Rong Wang (59795)</dc:creator>
          <dc:subject>Oncology and Carcinogenesis not elsewhere classified</dc:subject>
          <dc:subject>epithelial-mesenchymal transition</dc:subject>
          <dc:subject>GATA2</dc:subject>
          <dc:subject>invasion</dc:subject>
          <dc:subject>Jam2</dc:subject>
          <dc:subject>migration</dc:subject>
          <dc:subject>transcriptional regulation</dc:subject>
          <dc:subject>uterine corpus endometrial carcinoma</dc:subject>
          <dc:subject>ZNF486</dc:subject>
          <dc:description>Objective&lt;p&gt;To investigate the role and molecular mechanism of the GATA2/ZNF486/JAM2 transcriptional regulatory axis in the invasion and migration of Uterine Corpus Endometrial Carcinoma (UCEC).&lt;/p&gt;Methods&lt;p&gt;We employed reverse transcription quantitative polymerase chain reaction (RT-qPCR) and Western blot (WB) to assess the expression levels of ZNF486, GATA2, and JAM2 in UCEC cell lines. Lentivirus-mediated overexpression and knockdown cell lines were established, and CCK-8, colony formation, Transwell, and wound healing assays were performed to evaluate cell proliferation, invasion, and migration. WB and immunofluorescence were used to detect changes in epithelial-mesenchymal transition (EMT) markers. The direct binding and transcriptional activation of target gene promoters by transcription factors were confirmed through ChIP-qPCR and dual-luciferase reporter assays.&lt;/p&gt;Results&lt;p&gt;ZNF486 was significantly downregulated in UCEC. Its overexpression upregulated E-cadherin, downregulated N-cadherin and Vimentin, and markedly inhibited cell proliferation, invasion, and migration. Mechanistically, ZNF486 directly bound to and transcriptionally activated the JAM2 promoter; knockdown of JAM2 partially attenuated the tumor-suppressive effects of ZNF486. Furthermore, GATA2 was identified as an upstream transcription factor that directly activated ZNF486 transcription; knockdown of ZNF486 abrogated the tumor-suppressive effects induced by GATA2 overexpression.&lt;/p&gt;Conclusion&lt;p&gt;GATA2 inhibits EMT, invasion, and migration in UCEC by transcriptionally activating the ZNF486-JAM2 axis. This pathway provides a potential molecular framework for understanding UCEC progression.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-15T04:30:04Z</dc:date>
          <dc:type>Dataset</dc:type>
          <dc:type>Dataset</dc:type>
          <dc:identifier>10.3389/fonc.2026.1931641</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Supplementary_file_1_GATA2-driven_ZNF486-JAM2_activation_collaboratively_counteracts_epithelial-mesenchymal_transition_and_in_vitro_invasion_in_endometrial_cancer_docx/33771097</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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