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    <identifier>10.57760/sciencedb.02892</identifier>
    <datestamp>2022-09-27T14:10:49Z</datestamp>
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  <dc:date>2022-09-27</dc:date>
  <dc:title>Micheliolide Enhances Radiosensitivities Dataset</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.02892</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>Micheliolide (MCL) has shown promising anti-inflammatory and anti-tumor efficacy. However, whether and how MCL enhances the sensitivity of non-small-cell lung cancer (NSCLC) to radiotherapy are still unknown. In the present paper, we found that MCL exerted a tumor cell killing effect on NSCLC cells in a dose-dependent manner, and MCL strongly sensitized p53-deficient NSCLC cells, but not the cells with wild-type p53 to irradiation (IR). Meanwhile, MCL markedly inhibited the expression of hypoxia-inducible factor-1&amp;alpha; (HIF-1&amp;alpha;) after IR and hypoxic exposure in H1299 and Calu-1 cells rather than in H460 cells. Consistently, radiation- or hypoxia-induced expression of vascular endothelial growth factor (VEGF) was also significantly inhibited by MCL in H1299 and Calu-1 cells, but not in H460 cells. Therefore, inhibition of the HIF-1&amp;alpha; pathway might, at least in part, contribute to the radiosensitizing effect of MCL. Further study showed that MCL could accelerate the degradation of HIF-1&amp;alpha; through the ubiquitin-proteosome system. In addition, the transfection of wild-type p53 into p53-null cells (H1299) attenuated the effect of MCL on inhibiting HIF-1&amp;alpha; expression. These results suggest MCL effectively sensitizes p53-deficient NSCLC cells to IR in a manner of inhibiting the HIF-1&amp;alpha; pathway via promoting HIF-1&amp;alpha; degradation, and p53 played a negative role in MCL-induced HIF-1&amp;alpha; degradation.</dc:description>
  <dc:subject>micheliolide; radiosensitizer; hypoxia-inducible factor-1α; vascular endothelial growth factor; p53</dc:subject>
  <dc:creator>Peizhong Kong</dc:creator>
  <dc:creator>Wei Han</dc:creator>
  <dc:rights>PUBLIC</dc:rights>
  <dc:rights>https://creativecommons.org/licenses/by/4.0/</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:relation>http://www.doi.org/10.3390/ijms21093392</dc:relation>
  <dc:publisher>Science Data Bank</dc:publisher>
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