Home General Physiology and Biophysics 2022 General Physiology and Biophysics Vol.41, No.4, p. 263–274, 2022

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Founded: 1982
ISSN  1338-4325 (online)

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General Physiology and Biophysics Vol.41, No.4, p. 263–274, 2022

Title: Induction of apoptosis through inactivation of ROS-dependent PI3K/Akt signaling pathway by platycodin D in human bladder urothelial carcinoma cells
Author: Cheol Park, Hee-Jae Cha, Hyesook Lee, Jin-Woo Jeong, Min Ho Han, Kyoung Seob Song, Gi-Young Kim, Young-Chae Chang, Sun-Hee Leem, Jin Won Hyun, Heui-Soo Kim, Su Hyun Hong, Yung Hyun Choi

Abstract: Platycodin D (PD) is a triterpenoid saponin, a major bioactive constituent of the roots of Platycodon grandiflorum, which is well known for possessing various pharmacological properties. However, the anti-cancer mechanism of PD in bladder cancer cells remains poorly understood. In the current study, we investigated the effect of PD on the growth of human bladder urothelial carcinoma cells. PD treatment significantly reduced the cell survival of bladder cancer cells associated with induction of apoptosis and DNA damage. PD inhibited the expression of inhibitor of apoptosis family members, activated caspases, and induced cleavage of poly (ADP-ribose) polymerase. PD also increased the release of cytochrome c into the cytoplasm by disrupting the mitochondrial membrane potential while upregulating the expression ratio of Bax to Bcl-2. The PD-mediated anti-proliferative effect was significantly inhibited by pre-treatment with a pan-caspase inhibitor, but not by an inhibitor of necroptosis. Moreover, PD suppressed the phosphoinositide 3-kinase (PI3K)/Akt/mammalian target of rapamycin (mTOR) signaling pathway, and the apoptosis-inducing effect of PD was further enhanced by a PI3K inhibitor. In addition, PD increased the accumulation of reactive oxygen species (ROS), whereas N-acetyl cysteine (NAC), an ROS inhibitor, significantly attenuated the growth inhibition and inactivation of the PI3K/Akt/mTOR signaling caused by PD. Furthermore, NAC significantly suppressed apoptosis, DNA damage, and decreased cell viability induced by PD treatment. Collectively, our findings indicated that PD blocked the growth of bladder urothelial carcinoma cells by inducing ROS-mediated inactivation of the PI3K/Akt/mTOR signaling.

Keywords: Platycodin D — Apoptosis — ROS — PI3K/Akt/mTOR
Published online: 28-Jul-2022
Year: 2022, Volume: 41, Issue: 4 Page From: 263, Page To: 274
doi:10.4149/gpb_2022013


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