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Leaf extract of Osbeckia octandra induces apoptosis in oral squamous cell carcinoma cells

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dc.contributor.author김진-
dc.contributor.author김주영-
dc.date.accessioned2022-12-22T01:25:37Z-
dc.date.available2022-12-22T01:25:37Z-
dc.date.issued2022-01-
dc.identifier.issn*-
dc.identifier.urihttps://ir.ymlib.yonsei.ac.kr/handle/22282913/191212-
dc.description.abstractBackground: Osbeckia octandra is a plant endemic to Sri Lanka and is used in ethnomedicine for treating various diseases. However, the anti-cancer properties of O. octandra are yet to be fully investigated. In the present study, we evaluated the anti-cancer effects of O. octandra on oral cancer cells. Methods: Human oral cancer cell lines (HSC2, YD10B, YD38, YD9, and YD32) were used in this study. BrdU incorporation, cell cycle and annexin-V/PI staining were all evaluated using flow cytometry to determine the extent to which O. octandra leaf extract inhibits cell proliferation and induces apoptosis. Cell viability and reactive oxygen species (ROS) were also measured in order to investigate the anti-cancer effects of O. octandra extracts. Western blotting was performed to detect cell cycle related protein such as cyclin d1 and cdk4, and to detect apoptosis-related proteins such as Bcl-2, Bcl-XL, Bax, Caspase-9, Cleaved caspase-3, Fas, Caspase-8, and Bid. Results: Leaf extract of O. octandra reduced oral squamous cell carcinoma (OSCC) cell viability in a dose-dependent manner. Leaf extract of O. octandra has non-toxic in normal keratinocytes. Also, O. octandra extract interrupted the DNA replication via G1 phase arrests, and this effect was independent of ROS generation. In the apoptosis-related experiments, the population of annexin V-positive cells increased upon treatment with O. octandra extract. Furthermore, the expression of anti-apoptotic protein (Bcl-2 and Bcl-xL) was decreased, whereas the expression of cleaved caspase-3 protein was increased in O. octandra-treated OSCC cells. Conclusions: The results suggest that a leaf extract of O. octandra inhibited the proliferation of OSCC cells through G1 phase arrest and interrupting DNA replication. The leaf extract of O. octandra could trigger the apoptotic response via caspase 3 activation in OSCC cells. These results suggest that O. octandra has the potential to be developed as an alternative medicine for treating OSCC.-
dc.description.statementOfResponsibilityopen-
dc.formatapplication/pdf-
dc.languageEnglish-
dc.publisherBioMed Central-
dc.relation.isPartOfBMC COMPLEMENTARY MEDICINE AND THERAPIES-
dc.rightsCC BY-NC-ND 2.0 KR-
dc.subject.MESHAntineoplastic Agents, Phytogenic / pharmacology*-
dc.subject.MESHAntineoplastic Agents, Phytogenic / therapeutic use-
dc.subject.MESHApoptosis / drug effects-
dc.subject.MESHCarcinoma, Squamous Cell / drug therapy*-
dc.subject.MESHCell Line, Tumor / drug effects-
dc.subject.MESHHumans-
dc.subject.MESHMouth Neoplasms / drug therapy*-
dc.subject.MESHMyrtales*-
dc.subject.MESHPhytotherapy-
dc.subject.MESHPlant Extracts / pharmacology*-
dc.subject.MESHPlant Extracts / therapeutic use-
dc.subject.MESHSri Lanka-
dc.titleLeaf extract of Osbeckia octandra induces apoptosis in oral squamous cell carcinoma cells-
dc.typeArticle-
dc.contributor.collegeCollege of Dentistry (치과대학)-
dc.contributor.departmentDept. of Oral Pathology (구강병리학교실)-
dc.contributor.googleauthorJue Young Kim-
dc.contributor.googleauthorJin Kim-
dc.contributor.googleauthorB M Ratnayake Bandara-
dc.contributor.googleauthorWanninayake M Tilakaratne-
dc.contributor.googleauthorDokyeong Kim-
dc.identifier.doi10.1186/s12906-022-03505-4-
dc.contributor.localIdA01009-
dc.relation.journalcodeJ04368-
dc.identifier.eissn2662-7671-
dc.identifier.pmid35078428-
dc.subject.keywordApoptosis-
dc.subject.keywordCell cycle arrest-
dc.subject.keywordOral squamous cell carcinoma-
dc.subject.keywordOsbeckia octandra-
dc.contributor.alternativeNameKim, Jin-
dc.contributor.affiliatedAuthor김진-
dc.citation.volume22-
dc.citation.number1-
dc.citation.startPage20-
dc.identifier.bibliographicCitationBMC COMPLEMENTARY MEDICINE AND THERAPIES, Vol.22(1) : 20, 2022-01-
Appears in Collections:
2. College of Dentistry (치과대학) > Dept. of Oral Pathology (구강병리학교실) > 1. Journal Papers

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