Faculty Opinions recommendation of Twist, a master regulator of morphogenesis, plays an essential role in tumor metastasis.

Author(s):  
Daniel Flynn
Cell ◽  
2004 ◽  
Vol 117 (7) ◽  
pp. 927-939 ◽  
Author(s):  
Jing Yang ◽  
Sendurai A Mani ◽  
Joana Liu Donaher ◽  
Sridhar Ramaswamy ◽  
Raphael A Itzykson ◽  
...  

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yuqing Wang ◽  
Wei Wang ◽  
Haoming Wu ◽  
Yu Zhou ◽  
Xiaodan Qin ◽  
...  

AbstractMetastasis is the leading cause of cancer-related death. Despite the recent advancements in cancer treatment, there is currently no approved therapy for metastasis. The present study reveals a potent and selective activity of PRAK in the regulation of tumor metastasis. While showing no apparent effect on the growth of primary breast cancers or subcutaneously inoculated tumor lines, Prak deficiency abrogates lung metastases in PyMT mice or mice receiving intravenous injection of tumor cells. Consistently, PRAK expression is closely associated with metastatic risk in human cancers. Further analysis indicates that loss of function of PRAK leads to a pronounced inhibition of HIF-1α protein synthesis, possibly due to reduced mTORC1 activities. Notably, pharmacological inactivation of PRAK with a clinically relevant inhibitor recapitulates the anti-metastatic effect of Prak depletion, highlighting the therapeutic potential of targeting PRAK in the control of metastasis.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Nan Zhao ◽  
Huizhi Sun ◽  
Baocun Sun ◽  
Dongwang Zhu ◽  
Xiulan Zhao ◽  
...  

2012 ◽  
Vol 40 (1) ◽  
pp. 44-50 ◽  
Author(s):  
John S. O'Neill ◽  
Akhilesh B. Reddy

Approximately daily, or circadian, rhythms are ubiquitous across eukaryotes. They are manifest in the temporal co-ordination of metabolism, physiology and behaviour, thereby allowing organisms to anticipate and synchronize with daily environmental cycles. Although cellular rhythms are self-sustained and cell-intrinsic, in mammals, the master regulator of timekeeping is localized within the hypothalamic SCN (suprachiasmatic nucleus). Molecular models for mammalian circadian rhythms have focused largely on transcriptional–translational feedback loops, but recent data have revealed essential contributions by intracellular signalling mechanisms. cAMP and Ca2+ signalling are not only regulated by the cellular clock, but also contribute directly to the timekeeping mechanism, in that appropriate manipulations determine the canonical pacemaker properties of amplitude, phase and period. It is proposed that daily auto-amplification of second messenger activity, through paracrine neuropeptidergic coupling, is necessary and sufficient to account for the increased amplitude, accuracy and robustness of SCN timekeeping.


2011 ◽  
Vol 71 (13) ◽  
pp. 4329-4333 ◽  
Author(s):  
Pradip Raychaudhuri ◽  
Hyun Jung Park

Author(s):  
Ming Kong ◽  
Yuwen Zhu ◽  
Jing Shao ◽  
Zhiwen Fan ◽  
Yong Xu

Sterol response element binding protein (SREBP) is a master regulator of cellular lipogenesis. One key step in the regulation of SREBP activity is its sequential cleavage and trans-location by several different proteinases including SREBP cleavage activating protein (SCAP). We have previously reported that Brahma related gene 1 (BRG1) directly interacts with SREBP1c and SREBP2 to activate pro-lipogenic transcription in hepatocytes. We report here that BRG1 deficiency resulted in reduced processing and nuclear accumulation of SREBP in the murine livers in two different models of non-alcoholic steatohepatitis (NASH). Exposure of hepatocytes to lipopolysaccharide (LPS) and palmitate (PA) promoted SREBP accumulation in the nucleus whereas BRG1 knockdown or inhibition blocked SREBP maturation. Further analysis revealed that BRG1 played an essential role in the regulation of SCAP expression. Mechanistically, BRG1 interacted with Sp1 and directly bound to the SCAP promoter to activate SCAP transcription. Forced expression of exogenous SCAP partially rescued the deficiency in the expression of SREBP target genes in BRG1-null hepatocytes. In conclusion, our data uncover a novel mechanism by which BRG1 contributes to SREBP-dependent lipid metabolism.


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