Anti-Tumor Activity of Eurycoma longifolia Root Extracts against K-562 Cell Line In Vitro and In Vivo Study.docVIP
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Anti-Tumor Activity of Eurycoma longifolia Root Extracts against K-562 Cell Line In Vitro and In Vivo Study
Anti-TumorActivityofEurycomalongifoliaRootExtracts
againstK-562CellLine:InVitroandInVivoStudy
OmarSaeedAliAl-Salahi1.,DanJi2.,AminMalikShahAbdulMajid3,ChanKit-Lam3,
WanZaidahAbdullah4,AbdelhamidZaki1,5,ShahKamalKhanJamalDin6,NarazahMohdYusoff1*,
AmanShahAbdulMajid1*.
1AdvancedMedicalandDentalInstitute(AMDI),UniversitiSainsMalaysia(USM),KepalaBatas,PulauPinang,Malaysia,2KeyLabofVisualDamageandRegeneration
RestorationofChongqing,SouthwestEyeHospital,SouthwestHospital,TheThirdMilitaryMedicalUniversity,Chongqing,P.R.China,3SchoolofPharmaceuticalSciences,
UniversitiSainsMalaysia,Penang,Malaysia,4HaematologyDepartment,SchoolofMedicalSciences,USM,KubangKerian,Kelantan,Malaysia,5TherapeuticChemistry
Department,NationalResearchCentre,CairoUniversity,Dokki,Cairo,Egypt,6OMFSurgery,HospitalSultanahBhiyah,AlorSetar,Kedah,Malaysia
Abstract
Eurycoma longifolia Jack has been widely used in traditional medicine for its antimalarial, aphrodisiac, anti-diabetic,
antimicrobial and anti-pyretic activities. Its anticancer activity has also been recently reported on different solid tumors,
howevernoanti-leukemicactivityofthisplanthasbeenreported.Thusthepresentstudyassessestheinvitroandinvivo
anti-proliferativeandapoptoticpotentialsofE.longifoliaonK-562leukemiccellline.TheK-562cells(purchasedfromATCC)
wereisolatedfrompatientswithchronicmyelocyticleukemia(CML)weretreatedwiththevariousfractions(TAF273,F3and
F4) of E. longifolia root methanolic extract at various concentrations and time intervals and the anti-proliferative activity
assessed by MTS assay. Flow cytometry was used to assess the apoptosis and cell cycle arrest. Nude mice injected
subcutaneously with 107K-562 cells were used to study the anti-leukemic activity of TAF273 in vivo. TAF273, F3 and F4
showed various degrees of growth inhibition with IC50 values of 19, 55 and 62mg/ml, respectively. TAF273 induced
apoptosis in a dose and time dependent manner. TAF273 arrested cell cycle at G1and S phases. Intraperitoneal
administration
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