scholarly journals Molecular Characterization and Expression Pattern of Tripartite Motif Protein 39 in Gallus gallus with a Complete PRY/SPRY Domain

2011 ◽  
Vol 12 (6) ◽  
pp. 3797-3809 ◽  
Author(s):  
Chunqing Pan ◽  
Heng Zhao ◽  
Lin Shen ◽  
Jiping Sheng
2018 ◽  
Vol 79 ◽  
pp. 42-51 ◽  
Author(s):  
Julan Kim ◽  
Ju-Won Kim ◽  
Dong-Gyun Kim ◽  
Bo-Hye Nam ◽  
Young-Ok Kim ◽  
...  

2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Je-Jung Lee ◽  
In Ho Park ◽  
Man Sup Kwak ◽  
Woo Joong Rhee ◽  
Songhee H. Kim ◽  
...  

AbstractAlthough cellular senescence has emerged as a novel therapeutic concept in cancer, its underlying mechanisms remain unclear. High mobility group box 1 (HMGB1) and stimulator of interferon genes (STING) are involved in senescence. However, their interactions in senescence have not been reported. Therefore, in this study, we investigated the relationships between HMGB1 and STING in senescence in cancer and other cells. In mouse melanoma cells and several other cell lines, doxorubicin treatment induced senescence in an HMGB1-dependent manner. These responses were mediated by STING, and this function of STING was negatively regulated by the E3 ligase tripartite motif protein 30α (TRIM30α). We also found that HMGB1 bound to the TRIM30α promoter and then suppressed its expression by inhibiting its transcription, which enhanced STING-induced senescence. This mechanism was further mediated by signal transducer and activator of transcription 6 (STAT6) and p21. Overall, our findings demonstrated that HMGB1 orchestrated STING-STAT6-p21-mediated senescence by regulating TRIM30α as an alternative anticancer mechanism.


2009 ◽  
Vol 71 (4-5) ◽  
pp. 469-481 ◽  
Author(s):  
Xiaoxia Dai ◽  
Changjun You ◽  
Lei Wang ◽  
Guoxing Chen ◽  
Qifa Zhang ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document