http://purl.uniprot.org/citations/32432742 | http://www.w3.org/1999/02/22-rdf-syntax-ns#type | http://purl.uniprot.org/core/Journal_Citation |
http://purl.uniprot.org/citations/32432742 | http://www.w3.org/2000/01/rdf-schema#comment | "ObjectiveIncreasing evidence has shown that autophagy related proteins and hypoxia-inducible factor-1α (HIF-1α) are both involved in the malignant progress of nasopharyngeal carcinoma (NPC), and HIF-1α plays an emerging role in the chemosensitivity of NPC cells. However, it is still unknown whether autophagy related proteins are associated with HIF-1α in regulating the chemosensitivity of NPC cells.Materials and methodsQuantitative Real-time PCR (qPCR) was applied to determine mRNA levels of HIF-1α and the autophagy related proteins, such as ATG3, ATG4B, ATG5, Beclin1, ATG7, ATG10, ATG12 and ATG16L1. Western blot was applied to determine protein levels of HIF-1α, ATG4B and cleaved Caspase-3. Cell viability and death were investigated by cell counting kit-8 and trypan blue exclusion assay. In addition, Caspase-3 activity was detected to reflect apoptosis. Furthermore, Luciferase reporter assay was applied to explore the mechanism by which HIF-1α transcriptionally upregulated ATG4B expression.ResultsOur study reveals that HIF-1α increased ATG4B expression in NPC cells, and in turn upregulated the cisplatin (DDP)-induced protective autophagy, resulting in enhanced killing effect of DDP to NPC cells. In mechanism, reporter assay showed that HIF-1α upregulated ATG4B expression by activating its gene promoter region. The binding site (-225 to -216) was required for HIF-1α-induced increase of ATG4B gene promoter activity.ConclusionsThese results indicate that HIF-1α elevates ATG4B via promoting its transcription, which alleviates the sensitivity of DDP in NPC cells through enhancing protective autophagy, suggesting that ATG4B, upregulated by HIF-1α, may be a novel target for DDP sensitization in the treatment of NPC in clinic."xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.org/dc/terms/identifier | "doi:10.26355/eurrev_202005_21168"xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/author | "Huang J."xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/author | "Yu S."xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/author | "Yuan F."xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/author | "Li H.B."xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/author | "Lou Z.P."xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/date | "2020"xsd:gYear |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/name | "Eur Rev Med Pharmacol Sci"xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/pages | "4793-4802"xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/title | "Autophagy related 4B, upregulated by HIF-1alpha, attenuates the sensitivity to cisplatin in nasopharyngeal carcinoma cells."xsd:string |
http://purl.uniprot.org/citations/32432742 | http://purl.uniprot.org/core/volume | "24"xsd:string |
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