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作 者:Naglaa M.El-Lakkany Hadeel H.Elkattan Alaa E.Elsisi
机构地区:[1]Department of Pharmacology,Theodor Bilharz Research Institute,Warrak El-Hadar,Imbaba,Giza 12411,Egypt [2]Department of Pharmacology and Toxicology,Faculty of Pharmacy,Tanta University,Tanta,Egypt
出 处:《Asian Pacific Journal of Tropical Biomedicine》2023年第3期131-138,共8页亚太热带生物医学杂志(英文版)
基 金:financial support from the Theodor Bilharz Research Institute;Warrak El-Hadar;Imbaba;Giza 12411,Egypt。
摘 要:Objective:To evaluate the efficacy of ponatinib plus gossypol against colorectal cancer HCT-116 and Caco-2 cells.Methods:Cells were treated with ponatinib and/or gossypol at increasing concentrations to evaluate synergistic drug interactions by combination index.Cell viability,FGF19/FGFR4,and apoptotic and autophagic cell death were studied.Results:Ponatinib(1.25-40μM)and gossypol(2.5-80μM)monotherapy inhibited HCT-116 and Caco-2 cell viability in a doseand time-dependent manner.The combination of ponatinib and gossypol at a ratio of 1 to 2 significantly decreased cell viability(P<0.05),with a>2-and>4-fold reduction in IC50,respectively,after 24 h and 48 h,as compared to the IC50 of ponatinib.Lower combined concentrations showed greater synergism(combination index<1)with a higher ponatinib dose reduction index.Moreover,ponatinib plus gossypol induced morphological changes in HCT-116and Caco-2 cells,increased beclin-1 and caspase-3,and decreased FGF19,FGFR4,Bcl-2 and p-Akt as compared to treatment with drugs alone.Conclusions:Gossypol enhances ponatinib's anticancer effects against colorectal cancer cells through antiproliferative,apoptotic,and autophagic mechanisms.This may open the way for the future use of ponatinib at lower doses with gossypol as a potentially safer targeted strategy for colorectal cancer treatment.
关 键 词:AUTOPHAGY APOPTOSIS Cell viability FGF19/FGFR4 GOSSYPOL PONATINIB HCT-116 CACO-2 Colorectal cancer
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