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    <identifier>10.57760/sciencedb.09822</identifier>
    <datestamp>2023-08-20T14:46:18Z</datestamp>
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  <dc:date>2023-08-20</dc:date>
  <dc:title>MEHP activates JNK to inhibit the migration of human foreskin fibroblasts</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.09822</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>This study aimed to investigate the impact of mono(2-ethylhexyl) phthalate (MEHP) on the proliferation, apoptosis, and migration of human foreskin fibroblasts&amp;nbsp;cells (HFF-1) and the role of the JNK signaling pathway in cell migration. HFF-1 cells were randomly assigned to the control group with 0 MEHP exposure (M0) or the experimental groups with 25, 50, 100, 200, and 400 &amp;mu;mol/L MEHP exposure (M25, M50, M100, M200, and M400, respectively). After 24 and 48 h of MEHP exposure, the proliferation of HFF-1 cells in any group had no significant change. However, compared with the M0 group, the M200 and M400 groups presented substantially&amp;nbsp;increased apoptosis of HFF-1 cells. Moreover, cell migration ability significantly decreased in all groups (P &amp;lt; 0.05). Additionally, the transcription and phosphorylated protein activation of JNK kinase in HFF-1 cells were substantially&amp;nbsp;upregulated with the increase in MEHP exposure. Subsequently, HFF-1 cells were randomly divided into three groups: the DMSO blank control group, the 100 &amp;mu;M MEHP experimental group (M100), and the 100 &amp;mu;M MEHP plus 10 &amp;mu;M SP600125 (specific JNK inhibitor) experimental group (S10). The activation of JNK protein in HFF-1 cells was substantially&amp;nbsp;downregulated in the S10 group. HFF-1 cells were also divided into the blank control group (M0). They were treated with 100 &amp;mu;M MEHP and varying concentrations of SP600125 (5, 10, and 15 &amp;mu;M for S5, S10, and S15, respectively). As the concentration of the antagonist increased, the migration ability of HFF-1 cells was returned to normal. Finally, the ROS in HFF-1 cells increased under MEHP exposure. This finding indicates that the regulation of cell migration by the JNK signaling pathway plays an important role in the occurrence of hypospadias.</dc:description>
  <dc:subject>MEHP; HFF-1; JNK; cell migration</dc:subject>
  <dc:creator>Guoqiang Zhu</dc:creator>
  <dc:creator>Mingyong Li, PhD</dc:creator>
  <dc:creator>Xuan Yi</dc:creator>
  <dc:creator>Hu Zhang</dc:creator>
  <dc:creator>Wei Hu</dc:creator>
  <dc:creator>Xiaowen Fu</dc:creator>
  <dc:creator>Wei Jin</dc:creator>
  <dc:creator>Long Qin</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/publicdomain/zero/1.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:relation>http://www.doi.org/10.1080/19396368.2023.2262082</dc:relation>
  <dc:publisher>Science Data Bank</dc:publisher>
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