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dc.creatorYiallouris A., Patrikios I., Johnson E.O., Sereti E., Dimas K., De Ford C., Fedosova N.U., Graier W.F., Sokratous K., Kyriakou K., Stephanou A.en
dc.date.accessioned2023-01-31T11:37:53Z
dc.date.available2023-01-31T11:37:53Z
dc.date.issued2018
dc.identifier10.1038/s41419-018-0772-x
dc.identifier.issn20414889
dc.identifier.urihttp://hdl.handle.net/11615/80889
dc.description.abstractIn the healthcare sector, phytocompounds are known to be beneficial by contributing or alleviating a variety of diseases. Studies have demonstrated the progressive effects of phytocompounds on immune-related diseases and to exhibit anticancer effects. Graviola tree is an evergreen tree with its extracts (leafs and seeds) been reported having anticancer properties, but the precise target of action is not clear. Using an in silico approach, we predicted that annonacin, an Acetogenin, the active agent found in Graviola leaf extract (GLE) to potentially act as a novel inhibitor of both sodium/potassium (NKA) and sarcoplasmic reticulum (SERCA) ATPase pumps. We were able to validate and confirm the in silico studies by showing that GLE inhibited NKA and SERCA activity in intact cells. In the present study, we also demonstrated the antiproliferative and anticancer effects of GLE in a variety of cancer cell lines with limited toxic effects on non-transformed cells. Moreover, our results revealed that known inhibitors of both NKA and SERCA pumps could also promote cell death in several cancer cell lines. In addition, a mouse xenograft cancer model showed GLE as able to reduce tumor size and progression. Finally, bioprofiling studies indicated a strong correlation between overexpression of both NKA and SERCA gene expression vs. survival rates. Overall, our results demonstrated that GLE can promote selective cancer cell death via inhibiting NKA and SERCA, and thus can be considered as a potential novel treatment for cancer. After molecular analysis of GLE by liquid chromatography-mass spectrometry and ESI-QTOF-MS analysis, it was found that the MS spectrum of the high abundant chromatographic peak purified sample highly consisted of annonacin. © 2018 The Author(s).en
dc.language.isoenen
dc.sourceCell Death and Diseaseen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85049735863&doi=10.1038%2fs41419-018-0772-x&partnerID=40&md5=b37e0011ff170d0ed9106bf117d1cdea
dc.subjectacetogeninen
dc.subjectadenosine triphosphatase (potassium sodium)en
dc.subjectalcoholen
dc.subjectannonacinen
dc.subjectsarcoplasmic reticulum calcium transporting adenosine triphosphataseen
dc.subjectadenosine triphosphatase (potassium sodium)en
dc.subjectannonacinen
dc.subjectantineoplastic agenten
dc.subjectfuran derivativeen
dc.subjectlactoneen
dc.subjectplant extracten
dc.subjectsarcoplasmic reticulum calcium transporting adenosine triphosphataseen
dc.subjectanimal experimenten
dc.subjectanimal modelen
dc.subjectAnnona muricataen
dc.subjectantineoplastic activityen
dc.subjectantiproliferative activityen
dc.subjectArticleen
dc.subjectcancer cell destructionen
dc.subjectcancer cell lineen
dc.subjectcomputer modelen
dc.subjectgene overexpressionen
dc.subjectin vitro studyen
dc.subjectliquid chromatography-mass spectrometryen
dc.subjectmouseen
dc.subjectnonhumanen
dc.subjectplant leafen
dc.subjectpriority journalen
dc.subjectthin layer chromatographyen
dc.subjecttumor regressionen
dc.subjecttumor volumeen
dc.subjecttumor xenograften
dc.subjectanimalen
dc.subjectAnnonaen
dc.subjectcell deathen
dc.subjectchemistryen
dc.subjectdrug effecten
dc.subjectdrug screeningen
dc.subjectmetabolismen
dc.subjectpancreas tumoren
dc.subjectsignal transductionen
dc.subjecttandem mass spectrometryen
dc.subjectAnimalsen
dc.subjectAnnonaen
dc.subjectAntineoplastic Agentsen
dc.subjectCell Deathen
dc.subjectChromatography, Thin Layeren
dc.subjectFuransen
dc.subjectLactonesen
dc.subjectMiceen
dc.subjectPancreatic Neoplasmsen
dc.subjectPlant Extractsen
dc.subjectSarcoplasmic Reticulum Calcium-Transporting ATPasesen
dc.subjectSignal Transductionen
dc.subjectSodium-Potassium-Exchanging ATPaseen
dc.subjectTandem Mass Spectrometryen
dc.subjectXenograft Model Antitumor Assaysen
dc.subjectNature Publishing Groupen
dc.titleAnnonacin promotes selective cancer cell death via NKA-dependent and SERCA-dependent pathwaysen
dc.typejournalArticleen


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