scholarly journals PGD2/PTGDR2 Signaling Restricts the Self-Renewal and Tumorigenesis of Gastric Cancer

Stem Cells ◽  
2018 ◽  
Vol 36 (7) ◽  
pp. 990-1003 ◽  
Author(s):  
Bin Zhang ◽  
Qingli Bie ◽  
Peipei Wu ◽  
Jie Zhang ◽  
Benshuai You ◽  
...  
Keyword(s):  
The Self ◽  
2019 ◽  
Author(s):  
Liyan Wang ◽  
Bin Li ◽  
Xuhua Xiao ◽  
Xiaoyuan Yi ◽  
Feifei He

AbstractGastric cancer is one of the most serious cancers all over the world. Gastric tumor initiating cells (TIC) account for gastric tumorigenesis and metastasis. Here we identified circGTIC1 as a highly expressed circRNA in gastric cancer and gastric TICs. circGTIC1 knockout inhibited the self-renewal of gastric TICs and metastasis, and its overexpression activated gastric TICs. circGTIC1 drove the expression of Sox8 and exerted its role via Sox8-dependent manner. circGTIC1 associated with Ino80 chromatin remodeling complex, and recruited Ino80 complex to Sox8 promoter, finally initiated Sox8 expression. Our work revealed a novel circRNA to regulate gastric tumorigenesis and gastric TICs, adding a new layer for gastric TIC regulation and circRNA functions. CircGTIC1 plays a central role in gastric TIC self-renewal and metastasis. circGTIC1 drives the expression of Sox8 through recruiting Ino80 complex to Sox8 promoter. circGTIC1-Ino80-Sox8 axis can be used for gastric tumor and gastric TIC targeting. Our work revealed a novel circRNA to regulate gastric tumorigenesis and gastric TICs, adding a new layer for gastric TIC regulation and circRNA functions


2014 ◽  
Vol 50 (6) ◽  
pp. 645-656 ◽  
Author(s):  
Myoung-Eun Han ◽  
Hyun-Jung Kim ◽  
Dong Hoon Shin ◽  
Sun-Hwi Hwang ◽  
Chi-Dug Kang ◽  
...  

2015 ◽  
Vol 36 (6) ◽  
pp. 1657-1663 ◽  
Author(s):  
ZHENZHEN WEN ◽  
SHUJIONG FENG ◽  
LIJUAN WEI ◽  
ZHIMIN WANG ◽  
DEFEI HONG ◽  
...  

2013 ◽  
Vol 126 (18) ◽  
pp. 4220-4229 ◽  
Author(s):  
Q. Wu ◽  
Z. Yang ◽  
F. Wang ◽  
S. Hu ◽  
L. Yang ◽  
...  

2019 ◽  
Vol 14 (5) ◽  
pp. 428-436 ◽  
Author(s):  
Gabriele D. Bigoni-Ordóñez ◽  
Daniel Czarnowski ◽  
Tyler Parsons ◽  
Gerard J. Madlambayan ◽  
Luis G. Villa-Diaz

Cancer is a highly prevalent and potentially terminal disease that affects millions of individuals worldwide. Here, we review the literature exploring the intricacies of stem cells bearing tumorigenic characteristics and collect evidence demonstrating the importance of integrin α6 (ITGA6, also known as CD49f) in cancer stem cell (CSC) activity. ITGA6 is commonly used to identify CSC populations in various tissues and plays an important role sustaining the self-renewal of CSCs by interconnecting them with the tumorigenic microenvironment.


2020 ◽  
Vol 15 (6) ◽  
pp. 531-546 ◽  
Author(s):  
Hwa-Yong Lee ◽  
In-Sun Hong

Recent studies on the mechanisms that link metabolic changes with stem cell fate have deepened our understanding of how specific metabolic pathways can regulate various stem cell functions during the development of an organism. Although it was originally thought to be merely a consequence of the specific cell state, metabolism is currently known to play a critical role in regulating the self-renewal capacity, differentiation potential, and quiescence of stem cells. Many studies in recent years have revealed that metabolic pathways regulate various stem cell behaviors (e.g., selfrenewal, migration, and differentiation) by modulating energy production through glycolysis or oxidative phosphorylation and by regulating the generation of metabolites, which can modulate multiple signaling pathways. Therefore, a more comprehensive understanding of stem cell metabolism could allow us to establish optimal culture conditions and differentiation methods that would increase stem cell expansion and function for cell-based therapies. However, little is known about how metabolic pathways regulate various stem cell functions. In this context, we review the current advances in metabolic research that have revealed functional roles for mitochondrial oxidative phosphorylation, anaerobic glycolysis, and oxidative stress during the self-renewal, differentiation and aging of various adult stem cell types. These approaches could provide novel strategies for the development of metabolic or pharmacological therapies to promote the regenerative potential of stem cells and subsequently promote their therapeutic utility.


2021 ◽  
Vol 30 ◽  
pp. 096368972098511
Author(s):  
Gang Li ◽  
Xu Zhang ◽  
Xiangyang Guo ◽  
Yi Li ◽  
Chong Li

Bladder cancer is one of the most common malignancies. The existence of bladder cancer stem cells (BCSCs) has been suggested to underlie bladder tumor initiation and recurrence. Propofol is a commonly used intravenous anesthetic. Here, we find that propofol can dramatically block the activation of Hedgehog pathway in BCSCs. The propofol strongly repressed the growth of cancer cells. Attenuated proliferation and enhanced apoptosis of tumor cells were observed upon propofol stimulation. Furthermore, propofol reduced the self-renewal ability of BCSCs as well as the tumor formation. In conclusion, propofol is potentially used as a novel therapeutic agent for bladder cancer by targeting self-renewal through inhibiting Hedgehog pathway.


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