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    <responseDate>2026-10-14T13:31:48Z</responseDate>
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    <identifier>10.57760/sciencedb.45504</identifier>
    <datestamp>2026-08-05T15:23:57Z</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>2026-08-05</dc:date>
  <dc:title>Effects of Hedysari Radix before and after honey-processing paired with vinegar-processed Curcumae Rhizoma on apoptosis and autophagy of lung cancer cells-raw data</dc:title>
  <dc:identifier>doi:10.57760/sciencedb.45504</dc:identifier>
  <dc:language>en</dc:language>
  <dc:description>This study aims to compare the effects of honey processed Hedysari Radix-vinegar-processed&amp;nbsp;Curcumae Rhizoma&amp;nbsp;(HPHR-VPCR)&amp;nbsp;and Hedysari Radix-vinegar-processed&amp;nbsp;Curcumae Rhizoma&amp;nbsp;(HR-VPCR)&amp;nbsp;on apoptosis and autophagy in A549 cells and NCI-H1299 cells, and explore the mechanism of&amp;nbsp;HPHR-VPCR inducing&amp;nbsp;apoptosis and autophagy. Twenty-one SPF grade SD rats were randomly divided into three groups:&amp;nbsp;control&amp;nbsp;(Con) group, HR-VPCR&amp;nbsp;group, and HPHR-VPCR&amp;nbsp;group. The dosage of each drug pair was 4.63 g/kg, and the drug containing serum was taken after continuous administration for seven&amp;nbsp;days; Hoechst33258 staining was used to detect cell apoptosis morphology, and flow cytometry was used to detect cell apoptosis rate; The monodansylcadaverine (MDC) method was used to detect cellular autophagy; Transmission electron microscopy was used to detect autophagosomes and autolysosomes; Western blot was used to detect the expression of&amp;nbsp;ubiquitin-binding protein P62&amp;nbsp;(P62), beclin1(BECN1), B-cell lymphoma-2 (BCL-2), and BCL-2 associated X protein (BAX) proteins. The results of Hoechst33258 and flow cytometry analysis showed that in the groups treated with HR-VPCR&amp;nbsp;and HPHR-VPCR, chromatin accumulation, nuclear concentration and fragmentation were severe, apoptosis fluorescence was enhanced, and the proportion of apoptosis increased; The MDC method detection results showed that the green fluorescence of the HR-VPCR&amp;nbsp;group and HPHR-VPCR group was enhanced, and autophagosomes were increased; The Western blot results showed that compared with the blank group, the expression of P62 and BCL-2 proteins was significantly reduced in HPHR-VPCR&amp;nbsp;group, while the expression of BECN1&amp;nbsp;and BAX proteins was significantly increased (P&amp;lt;0.01, P&amp;lt;0.05). In summary, both HR-VPCR&amp;nbsp;and HPHR-VPCR&amp;nbsp;can induce cell apoptosis and autophagy. HPHR-VPCR&amp;nbsp;is superior to HR-VPCR&amp;nbsp;in inducing cell apoptosis and autophagy. The induction of apoptosis and autophagy in lung cancer cells by HPHR-VPCR&amp;nbsp;is related to the decrease of P62 and BCL-2, as well as the increase of BECN1&amp;nbsp;and BAX expression.</dc:description>
  <dc:subject>honey-processed Hedysari Radix-vinegar-processed Curcumae Rhizoma; Hedysari Radix-vinegar-processed Curcumae Rhizoma; apoptosis;  autophagy; lung cancer cells</dc:subject>
  <dc:creator>ma ding cai</dc:creator>
  <dc:rights>RESTRICTED</dc:rights>
  <dc:type>dataset</dc:type>
  <dc:publisher>Science Data Bank</dc:publisher>
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