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Suppression of NRF2/ARE by convallatoxin sensitises A549 cells to 5-FU-mediated apoptosis
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, June | - |
| dc.contributor.author | Kang, Jong-Su | - |
| dc.contributor.author | Nam, Le Ba | - |
| dc.contributor.author | Yoo, Ok-Kyung | - |
| dc.contributor.author | Keum, Young-Sam | - |
| dc.date.accessioned | 2023-04-28T06:40:45Z | - |
| dc.date.available | 2023-04-28T06:40:45Z | - |
| dc.date.issued | 2018-12-02 | - |
| dc.identifier.issn | 1071-5762 | - |
| dc.identifier.issn | 1029-2470 | - |
| dc.identifier.uri | https://scholarworks.dongguk.edu/handle/sw.dongguk/8700 | - |
| dc.description.abstract | NF-E2-related factor 2 (NRF2) regulates transcription of phase II cytoprotective enzymes to protect normal cells against oxidative stress. However, a high level of NRF2 offers a growth advantage, chemoresistance, and radioresistance in cancer. In the present study, we have identified convallatoxin as a novel inhibitor of NRF2/ARE. Suppression of NRF2 by convallatoxin was not transcriptionally mediated, but regulated at the level of proteolysis. Convallatoxin activated GSK-3 beta and suppression of NRF2 by convallatoxin required the Neh6 domain. Convallatoxin sensitised A549 cells to 5-fluorouracil-mediated cell death by promoting apoptosis. Together, our results provide evidence that convallatoxin might be useful as a chemotherapeutic adjuvant due to its ability to suppress NRF2/ARE. | - |
| dc.format.extent | 8 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | TAYLOR & FRANCIS LTD | - |
| dc.title | Suppression of NRF2/ARE by convallatoxin sensitises A549 cells to 5-FU-mediated apoptosis | - |
| dc.type | Article | - |
| dc.publisher.location | 영국 | - |
| dc.identifier.doi | 10.1080/10715762.2018.1489132 | - |
| dc.identifier.scopusid | 2-s2.0-85053306631 | - |
| dc.identifier.wosid | 000457432500021 | - |
| dc.identifier.bibliographicCitation | FREE RADICAL RESEARCH, v.52, no.11-12, pp 1416 - 1423 | - |
| dc.citation.title | FREE RADICAL RESEARCH | - |
| dc.citation.volume | 52 | - |
| dc.citation.number | 11-12 | - |
| dc.citation.startPage | 1416 | - |
| dc.citation.endPage | 1423 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Biochemistry & Molecular Biology | - |
| dc.relation.journalWebOfScienceCategory | Biochemistry & Molecular Biology | - |
| dc.subject.keywordPlus | KEAP1-NRF2 PATHWAY | - |
| dc.subject.keywordPlus | BETA-TRCP | - |
| dc.subject.keywordPlus | CANCER | - |
| dc.subject.keywordAuthor | 5-Fluorouracil (5-FU) | - |
| dc.subject.keywordAuthor | antioxidant response element (ARE) | - |
| dc.subject.keywordAuthor | convallatoxin | - |
| dc.subject.keywordAuthor | NRF2 | - |
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