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Cytotoxic 4-Hydroxyprorocentrolide and Prorocentrolide C from Cultured DinoflagellateProrocentrum limaInduce Human Cancer Cell Death through Apoptosis and Cell Cycle Arrest
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Lee, Seon Min | - |
| dc.contributor.author | Kim, Na-Hyun | - |
| dc.contributor.author | Jeong, Eun Ju | - |
| dc.contributor.author | Rho, Jung-Rae | - |
| dc.date.accessioned | 2022-12-26T12:47:25Z | - |
| dc.date.available | 2022-12-26T12:47:25Z | - |
| dc.date.issued | 2020-05 | - |
| dc.identifier.issn | 2072-6651 | - |
| dc.identifier.issn | 2072-6651 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/6635 | - |
| dc.description.abstract | Prorocentrolide and its analogs, the novel naturally derived antitumor agents, have recently been identified in the dinoflagellateProrocentrum lima. In the current study, the underlying inhibitory mechanisms of 4-hydroxyprorocentrolide (1) and prorocentrolide C (2) on the proliferation of human carcinoma cells were determined.1and2arrested the cell cycle at the S phase in A549 cells and G2/M phase in HT-29 cells, leading to apoptotic cell death, as determined using fluorescence-activated cell sorting analysis with Annexin V/PI double staining. Apoptosis induced by these compounds was associated with alterations in the expression of cell cycle-regulating proteins (cyclin D1, cyclin E1, CDK2, and CDK4), as well as alterations in the levels of apoptosis-related proteins (PPAR, Bcl-2, Bcl-xl, and survivin). These findings provide new insights into the antitumor mechanisms of 4-hydroxyprorocentrolide and prorocentrolide C and a basis for future investigations assessing prorocentrolide analogs as prospective therapeutic drugs. | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | MDPI | - |
| dc.title | Cytotoxic 4-Hydroxyprorocentrolide and Prorocentrolide C from Cultured DinoflagellateProrocentrum limaInduce Human Cancer Cell Death through Apoptosis and Cell Cycle Arrest | - |
| dc.type | Article | - |
| dc.publisher.location | 스위스 | - |
| dc.identifier.doi | 10.3390/toxins12050304 | - |
| dc.identifier.scopusid | 2-s2.0-85084468815 | - |
| dc.identifier.wosid | 000541799400003 | - |
| dc.identifier.bibliographicCitation | TOXINS, v.12, no.5 | - |
| dc.citation.title | TOXINS | - |
| dc.citation.volume | 12 | - |
| dc.citation.number | 5 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Food Science & Technology | - |
| dc.relation.journalResearchArea | Toxicology | - |
| dc.relation.journalWebOfScienceCategory | Food Science & Technology | - |
| dc.relation.journalWebOfScienceCategory | Toxicology | - |
| dc.subject.keywordPlus | INHIBITOR OKADAIC ACID | - |
| dc.subject.keywordPlus | PROTEIN PHOSPHATASES | - |
| dc.subject.keywordPlus | CACO-2 CELLS | - |
| dc.subject.keywordPlus | TOXIN | - |
| dc.subject.keywordPlus | GENOTOXICITY | - |
| dc.subject.keywordPlus | LIMA | - |
| dc.subject.keywordAuthor | Prorocentrum lima | - |
| dc.subject.keywordAuthor | prorocentrolide | - |
| dc.subject.keywordAuthor | cytotoxic | - |
| dc.subject.keywordAuthor | apoptosis | - |
| dc.subject.keywordAuthor | cell cycle arrest | - |
| dc.subject.keywordAuthor | cancer | - |
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