scholarly journals Analysis of genes regulated by DUX4 via oxidative stress reveals potential therapeutic targets for treatment of facioscapulohumeral dystrophy

Redox Biology ◽  
2021 ◽  
pp. 102008
Author(s):  
Anna Karpukhina ◽  
Ivan Galkin ◽  
Yinxing Ma ◽  
Carla Dib ◽  
Roman Zinovkin ◽  
...  
2018 ◽  
Vol 134 ◽  
pp. 208-217 ◽  
Author(s):  
Peiying Li ◽  
R. Anne Stetler ◽  
Rehana K. Leak ◽  
Yejie Shi ◽  
Yan Li ◽  
...  

2021 ◽  
Vol 28 ◽  
Author(s):  
Abeer Mohsin ◽  
Kanwal Haneef ◽  
Amber Ilyas ◽  
Shamshad Zarina ◽  
Zehra Hashim

Background: The increasing incidence and mortality rate of HCC is a major concern, especially for developing countries of the world. Hence, extensive research is being carried out in order to explore new approaches for developing successful therapeutic strategies for HCC. The controversial role of oxidative stress in the prognosis and treatment of various diseases such as cancer has become the area of great interest and intrigue for many scientists throughout the world. Objective: We aim to investigate the role of induced oxidative stress on the suppression of HCC Huh-7 cancerous cells as therapeutic approach. Methods: Induction of oxidative stress via H2O2 treatment produced cell cytotoxicity in a dose dependent manner and also led to the over expression of GSTP-1 and PRX-2. The expression of GSTP-1 and PRX-2 was compared in HCC Huh-7 treated, untreated cells and normal hepatocytes using immunocytochemistry. Furthermore, the effects of oxidative stress on cell cycle arrest were also studied through flow cytometry. Results: Our study demonstrated the inhibition of cancer cell proliferation as a result of H2O2 induction by arresting the cell cycle at G2 phase. Conclusion: The induction of oxidative stress could be a potential therapeutic approach for treating HCC in the future. GSTP-1 and PRX-2 can serve as substantial therapeutic targets for the treatment of HCC.


2013 ◽  
Vol 140 (3) ◽  
pp. 239-257 ◽  
Author(s):  
Luc Rochette ◽  
Julie Lorin ◽  
Marianne Zeller ◽  
Jean-Claude Guilland ◽  
Luc Lorgis ◽  
...  

2016 ◽  
Vol 108 ◽  
pp. 1-10 ◽  
Author(s):  
Sergio Portal-Núñez ◽  
Pedro Esbrit ◽  
María José Alcaraz ◽  
Raquel Largo

2020 ◽  
Vol 21 (14) ◽  
pp. 4962 ◽  
Author(s):  
Humna Bhagani ◽  
Suzanne A. Nasser ◽  
Ali Dakroub ◽  
Ahmed F. El-Yazbi ◽  
Assaad A. Eid ◽  
...  

Diabetic cardiomyopathy (DCM) is a constellation of symptoms consisting of ventricular dysfunction and cardiomyocyte disarray in the presence of diabetes. The exact cause of this type of cardiomyopathy is still unknown; however, several processes involving the mitochondria, such as lipid and glucose metabolism, reactive oxygen species (ROS) production, apoptosis, autophagy and mitochondrial biogenesis have been implicated. In addition, polyphenols have been shown to improve the progression of diabetes. In this review, we discuss some of the mechanisms by which polyphenols, particularly resveratrol, play a role in slowing the progression of DCM. The most important intermediates by which polyphenols exert their protective effect include Bcl-2, UCP2, SIRT-1, AMPK and JNK1. Bcl-2 acts to attenuate apoptosis, UCP2 decreases oxidative stress, SIRT-1 increases mitochondrial biogenesis and decreases oxidative stress, AMPK increases autophagy, and JNK1 decreases apoptosis and increases autophagy. Our dissection of these molecular players aims to provide potential therapeutic targets for the treatment of DCM.


2013 ◽  
Vol 62 (5) ◽  
pp. 764-775 ◽  
Author(s):  
Joshua A. Smith ◽  
Sookyoung Park ◽  
James S. Krause ◽  
Naren L. Banik

2016 ◽  
Vol 2016 ◽  
pp. 1-10 ◽  
Author(s):  
Zhanpeng Wang ◽  
Zhuonan Li ◽  
Yanshuo Ye ◽  
Lijuan Xie ◽  
Wei Li

Accumulating evidence has indicated that oxidative stress (OS) is associated with the development of hepatocellular carcinoma (HCC). However, the mechanisms remain largely unknown. Normally, OS occurs when the body receives any danger signal—from either an internal or external source—and further induces DNA oxidative damage and abnormal protein expression, placing the body into a state of vulnerability to the development of various diseases such as cancer. There are many factors involved in liver carcinogenesis, including hepatitis B virus (HBV) and hepatitis C virus (HCV) infection, alcohol abuse, and nonalcoholic fatty liver disease (NAFLD). The relationship between OS and HCC has recently been attracting increasing attention. Therefore, elucidation of the impact of OS on the development of liver carcinogenesis is very important for the prevention and treatment of liver cancer. This review focuses mainly on the relationship between OS and the development of HCC from the perspective of cellular and molecular mechanisms and the etiology and therapeutic targets of HCC.


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