A novel 7-azaisoindigo derivative-induced cancer cell apoptosis and mitochondrial dysfunction mediated by oxidative stress

2010 ◽  
pp. n/a-n/a
Author(s):  
Jing-jing Xu ◽  
Xiao-min Dai ◽  
Hai-liang Liu ◽  
Wen-jie Guo ◽  
Jing Gao ◽  
...  
2018 ◽  
Vol 9 (11) ◽  
pp. 5536-5546 ◽  
Author(s):  
Yang Wang ◽  
Yang-Jia Li ◽  
Xiao-Hui Huang ◽  
Can-Can Zheng ◽  
Xing-Feng Yin ◽  
...  

Functional screen and quantitative proteomics reveal that food-source liensinine induces colorectal cancer cell apoptosisviathe JNK-mitochondrial dysfunction signaling pathway.


2020 ◽  
Vol 11 (12) ◽  
pp. 3215-3222
Author(s):  
Xinming Li ◽  
Yanan Hou ◽  
Jintao Zhao ◽  
Jin Li ◽  
Song Wang ◽  
...  

The 1,2-diselenolane unit is a general scaffold to construct glutathione-dependent prodrugs that show increased potency to cancer cells, and work via a combination of chemotherapy and oxidative stress.


2012 ◽  
Vol 13 (3) ◽  
pp. 138-147 ◽  
Author(s):  
Wang Zhiyu ◽  
Cheng Yue ◽  
Wang Neng ◽  
Wang Dong Mei ◽  
Li Ying Wei ◽  
...  

2020 ◽  
Vol 22 (1) ◽  
pp. 155-164
Author(s):  
Jiuling Li ◽  
Yany Li ◽  
Lanlan Chen ◽  
Bingbing Yu ◽  
Yanan Xue ◽  
...  

2016 ◽  
Vol 4 (13) ◽  
pp. 2351-2358 ◽  
Author(s):  
Tianqi Nie ◽  
Hualian Wu ◽  
Ka-Hing Wong ◽  
Tianfeng Chen

Herein, we demonstrated a new and facial synthesis of highly uniformed SeNPs using glucose as the reductant and surface decorator. Glu–SeNPs induced cancer cell apoptosisviainduction of apoptosis by triggering intracellular ROS overproduction and mitochondrial dysfunction.


2008 ◽  
Vol 7 (8) ◽  
pp. 2319-2327 ◽  
Author(s):  
Jessica R. Kirshner ◽  
Suqin He ◽  
Vishwasenani Balasubramanyam ◽  
Jane Kepros ◽  
Chin-Yu Yang ◽  
...  

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Yu Wang ◽  
Liming Zhu ◽  
Mei Guo ◽  
Gang Sun ◽  
Kun Zhou ◽  
...  

AbstractWHSC1 is a histone methyltransferase that facilitates histone H3 lysine 36 dimethylation (H3K36me2), which is a permissive mark associated with active transcription. In this study, we revealed how WHSC1 regulates tumorigenesis and chemosensitivity of colorectal cancer (CRC). Our data showed that WHSC1 as well as H3K36me2 were highly expressed in clinical CRC samples, and high WHSC1 expression is associated with poorer prognosis in CRC patients. WHSC1 reduction promoted colon cancer cell apoptosis both in vivo and in vitro. We found that B cell lymphoma-2 (BCL2) expression, an anti-apoptotic protein, is markedly decreased in after WHSC1 depletion. Mechanistic characterization indicated that WHSC1 directly binds to the promoter region of BCL2 gene and regulate its H3K36 dimethylation level. What’s more, our study indicated that WHSC1 depletion promotes chemosensitivity in CRC cells. Together, our results suggested that WHSC1 and H3K36me2 modification might be optimal therapeutic targets to disrupt CRC progression and WHSC1-targeted therapy might potentially overcome the resistance of chemotherapeutic agents.


2020 ◽  
Vol 21 (10) ◽  
pp. 571-582
Author(s):  
Jia Qi Li ◽  
Jia Lu Li ◽  
Yuan Hong Xie ◽  
Yao Wang ◽  
Xiao Nan Shen ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document