scholarly journals Tussilago farfara L. augments TRAIL-induced apoptosis through MKK7/JNK activation by inhibition of MKK7-TIPRL in human hepatocellular carcinoma cells

2014 ◽  
Vol 32 (3) ◽  
pp. 1117-1123 ◽  
Author(s):  
HYO-JUNG LEE ◽  
HYUN-SOO CHO ◽  
SOO YOUNG JUN ◽  
JEONG-JU LEE ◽  
JI-YONG YOON ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Carcinoma Cells ◽  
Human Hepatocellular Carcinoma ◽  
Hepatocellular Carcinoma Cells ◽  
Tussilago Farfara ◽  
Induced Apoptosis ◽  
Jnk Activation ◽  
Human Hepatocellular Carcinoma Cells

scholarly journals 20(s)-ginsenoside Rh2 promotes TRAIL-induced apoptosis by upregulating DR5 in human hepatocellular carcinoma cells

2021 ◽  
Author(s):  
Wenmo Liu ◽  
Siqi Wang ◽  
Qinchuan Yang ◽  
Xinyao Feng ◽  
Bin Yu ◽  
...  
Keyword(s):  
Hepatocellular Carcinoma ◽  
Carcinoma Cells ◽  
Human Hepatocellular Carcinoma ◽  
Negative Regulator ◽  
Cancer Drug ◽  
Ginsenoside Rh2 ◽  
Apoptosis Pathway ◽  
Hepatocellular Carcinoma Cells ◽  
Induced Apoptosis ◽  
Human Hepatocellular Carcinoma Cells

Abstract Tumor necrosis factor-related apoptosis-inducing ligand (TRAIL) is a potential therapeutic anti-cancer drug with selective cytotoxicity in cancer cells. However, in multiple clinical trials, the therapeutic effect of TRAIL is limited owing to tumor resistance. The combination of small molecules or other drugs may represent a suitable strategy to overcome TRAIL resistance. This study found that 20(s)-ginsenoside Rh2 sensitized non-sensitive human hepatocellular carcinoma cells to TRAIL-induced apoptosis. The combination of TRAIL and Rh2 decreased cell viability and increased caspase cascade-induced apoptosis in several liver cancer cell lines. Moreover, we found that Rh2 reduced the apoptosis-related protein XIAP and Survivin, a negative regulator of the apoptosis pathway. At the same time, Rh2 can further enhance TRAIL-induced apoptosis by upregulating the death receptor 5 (DR5), thereby significantly enhancing its anti-tumor effect. Furthermore, Rh2 enhanced the therapeutic efficacy of TRAIL in mouse xenograft models, suggesting that Rh2 also sensitizes TRAIL in vivo. Taken together, our study indicates that Rh2 may act as a sensitizer in combination with TRAIL to increase the efficacy of its anti-tumor activity.

Sign in / Sign up

Export Citation Format

Share Document