Ferulic acid reverses P-glycoprotein-mediated multidrug resistance via inhibition of PI3K/Akt/NF-κB signaling pathway

被引:57
|
作者
Muthusamy, Ganesan [1 ]
Gunaseelan, Srithar [1 ]
Prasad, Nagarajan Rajendra [1 ]
机构
[1] Annamalai Univ, Dept Biochem & Biotechnol, Annamalainagar 608002, Tamil Nadu, India
关键词
Ferulic acid; Multidrug resistance; P-glycoprotein; NF-kappa B; Phosphatidyinositol; 3-kinase; NF-KAPPA-B; CELLS; EXPRESSION; DOXORUBICIN; CANCER; CHEMORESISTANCE; PROLIFERATION; TRANSCRIPTION; SUPPRESSION; MDR1;
D O I
10.1016/j.jnutbio.2018.09.022
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In this study, the modulatory effect of ferulic acid on P-glycoprotein (P-gp)-mediated multidrug resistance (MDR) was examined in KB Ch(R)8-5 resistant cells and drug-resistant tumor xenografts. We observed that ferulic acid enhanced the cytotoxicity of doxorubicin and vincristine in the P-gp overexpressing KB Ch(R)8-5 cells. Further, ferulic acid enhances the doxorubicin induced gamma H2AX foci formation and synergistically augmented doxorubicin-induced apoptotic signaling in the drug resistant cells. It has also been noticed that NF-kappa B nuclear translocation was suppressed by ferulic acid and that this response might be associated with the modulation of phosphatidyinositol 3-kinase (PI3K)/Akt/signaling pathway. We also found that ferulic acid and doxorubicin combination reduced the size of KB Ch(R)8-5 tumor xenograft by threefold as compared to doxorubicin-alone treated group. Thus, ferulic acid contributes to the reversal of the MDR through suppression of P-gp expression via the inhibition of PI3K/Akt/NF-kappa B signaling pathway. (C) 2018 Elsevier Inc. All rights reserved.
引用
收藏
页码:62 / 71
页数:10
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