Photoacoustic imaging of chemotherapy-induced apoptosis in squamous cell carcinoma

2012 ◽  
Author(s):  
Quihong Yang ◽  
Huizhong Cui ◽  
Shuang Cai ◽  
Xinmai Yang ◽  
M. Laird Forrest
2019 ◽  
Vol 17 (4) ◽  
pp. 463-469
Author(s):  
Hou Deqiang ◽  
Gao Yufeng ◽  
Bai Ning ◽  
Dong Yu

Isoliquiritigenin is a flavonoid commonly found in liquorice and has been identified as a potent anti-tumor agent. The aim of this study was to investigate whether isoliquiritigenin regulates the proliferation and apoptosis of tongue squamous cell carcinoma cells by regulating forkhead box G1 expression via miR-21. MTT assay and flow cytometry were used to analyze cell proliferation and apoptosis, respectively. Quantitative real time polymerase chain reaction and western blotting were used to detect mRNA and protein expression levels, respectively. The relationship between miR-21 and forkhead box G1 was detected by dual luciferase assay. Isoliquiritigenin inhibited proliferation and induced apoptosis of tongue squamous cell carcinoma cells, and decreased miR-21 levels and promoted forkhead box G1 expression. Forkhead box G1 was then identified as a target of miR-21 and ISL could promote forkhead box G1 expression by inhibiting miR-21. Further analysis suggested that upregulation of miR-21 improved proliferation and suppressed apoptosis of tongue squamous cell carcinoma cells by inhibiting forkhead box G1 expression. Finally, our results revealed that isoliquiritigenin inhibited proliferation and induced apoptosis of tongue squamous cell carcinoma cells by regulating miR-21. Isoliquiritigenin might act as a novel therapeutic treatment for tongue squamous cell carcinoma cells through up-regulation of forkhead box G1 expression via inhibiting miR-21expression.


2020 ◽  
Vol 21 (21) ◽  
pp. 7947
Author(s):  
Jing-Ru Weng ◽  
Wei-Yu Lin ◽  
Li-Yuan Bai ◽  
Jing-Lan Hu ◽  
Chia-Hsien Feng

We recently isolated a cardiac glycoside (CG), αldiginoside, from an indigenous plant in Taiwan, which exhibits potent tumor-suppressive efficacy in oral squamous cell carcinoma (OSCC) cell lines (SCC2095 and SCC4, IC50 < 0.2 µM; 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assays). Here, we report that αldiginoside caused Sphase arrest and apoptosis, through the inhibition of a series of signaling pathways, including those mediated by cyclin E, phospho-CDC25C (p-CDC25C), and janus kinase/signal transducer and activator of transcription (JAK/STAT)3. αldiginoside induced apoptosis, as indicated by caspase activation and poly (ADP-ribose) polymerase (PARP) cleavage. Equally important, αldiginoside reduced Mcl-1 expression through protein degradation, and overexpression of Mcl-1 partially protected SCC2095 cells from αldiginoside’s cytotoxicity. Taken together, these data suggest the translational potential of αldiginoside to foster new therapeutic strategies for OSCC treatment.


2019 ◽  
Vol 120 (8) ◽  
pp. 13893-13902 ◽  
Author(s):  
Wu Zhou ◽  
Shoumin Zhang ◽  
Jianguo Li ◽  
Zhenlu Li ◽  
Yuping Wang ◽  
...  

2020 ◽  
Vol 16 (15) ◽  
pp. 2883-2894
Author(s):  
Yinan Yao ◽  
Luyun Cui ◽  
Jiani Ye ◽  
Guangdie Yang ◽  
Guohua Lu ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document