3rd International conference on Natural Products for Cancer Prevention and Therapy, Kayseri, Türkiye, 18 - 20 Aralık 2019, cilt.40, ss.6
Kynurenic Acid (KYNA) is a metabolite of tryptophan pathway and also an endogenous
antagonist of glutamate receptors. Several studies indicated that glutamate antagonists have antiproliferative
potential. Moreover, subunits of the NMDA receptor which is one of the glutamate
receptors have been shown to be found in human hepatocellular carcinoma cell line (HepG2). In
this study, the antitumor effects of KYNA in HepG2 cells were investigated for the first time at the
molecular level. The effects of KYNA on the viability of HepG2 cells were determined by MTT
analyses. Effects of KYNA on mRNA transcriptions of apoptosis related genes Bax, Bcl-2 and
Caspase-3 were analyzed by qRT-PCR. mRNA expression analysis revealed that the mRNA levels
of effector Caspase-3 and pro-apoptotic Bax/Bcl-2 ratio were not increased in HepG2 cells treated
with KYNA. In conclusion, our findings showed that KYNA does not exert its anti-proliferative
effects on HepG2 cells through caspase-mediated apoptotic cell death, but it may perform this antiproliferative
effect through a different mechanism of death. Further studies are needed to find out
potential cell death mechanisms that may play a role in anti-proliferative activity of KYNA on
HepG2 cells.