Skip to main content
. 2016 Jun 28;8(7):396. doi: 10.3390/nu8070396

Table 1.

Summary of proposed beneficial effects of co-administration of mangiferin alongside chemotherapeutic agents.

Chemotherapeutic Agent Cell Line Reference Evidence
Oxaliplatin HeLa, HT29, HL60 [48] Reduction in oxaliplatin IC50 values; counteracts resistance to oxaliplatin.
Etoposide HL60, U937 [11,13] Reduces oxidative stress. Protects normal cells without reducing sensitivity of HL60 to etoposide [13]. Activity of the drug is enhanced by mangiferin [11].
Doxorubicin MCF7, U937 [13,33] At high concentrations mangiferin can inhibit P-glycoprotein expression and chemosensitise for doxorubicin therapy [33]. Activity of the drug is enhanced by mangiferin [11].
Paclitaxel Triple negative breast cancer [60,62] IRAK1 overexpression confers a growth advantage [62]. Mangiferin may inhibit IRAK1 activation [60,62].
Cisplatin U937 [11] Inhibits ROS production [8]. Activity of the drug is enhanced by mangiferin; Impedes NFκB activation; Enhanced cell death in the presence of TNF [11].
Vincristine U937 [11] Inhibits ROS production [8]. Activity of the drug is enhanced by mangiferin; Impedes NFκB activation; Enhanced cell death in the presence of TNF [11].
Adriamycin U937 [11] Inhibits ROS production [8]. Activity of the drug is enhanced by mangiferin; Impedes NFκB activation; Enhanced cell death in the presence of TNF [11].
AraC U937 [11] Inhibits ROS production [8]. Activity of the drug is enhanced by mangiferin; Impedes NFκB activation; Enhanced cell death in the presence of TNF [11].