scholarly journals Coptis japonica Makino extract suppresses angiogenesis through regulation of cell cycle-related proteins

2016 ◽  
Vol 80 (6) ◽  
pp. 1095-1106 ◽  
Author(s):  
Seo Ho Kim ◽  
Eok-Cheon Kim ◽  
Wan-Joong Kim ◽  
Myung-Hun Lee ◽  
Sun-Young Kim ◽  
...  
Hepatology ◽  
1998 ◽  
Vol 27 (3) ◽  
pp. 691-696 ◽  
Author(s):  
Lena C. E. Ohlson ◽  
Lena Koroxenidou ◽  
Inger Porsch Hällström

2007 ◽  
Vol 321 (2) ◽  
pp. 648-655 ◽  
Author(s):  
Yong Lim ◽  
Tack-Joong Kim ◽  
Yong-Ri Jin ◽  
Dong-Woon Kim ◽  
Jin-Sook Kwon ◽  
...  

2011 ◽  
Vol 2011 ◽  
pp. 1-12 ◽  
Author(s):  
Alfonso Baldi ◽  
Antonio De Luca ◽  
Vincenzo Esposito ◽  
Mara Campioni ◽  
Enrico P. Spugnini ◽  
...  

The cell cycle is the cascade of events that allows a growing cell to duplicate all its components and split into two daughter cells. Cell cycle progression is mediated by the activation of a highly conserved family of protein kinases, the cyclin-dependent kinases (CDKs). CDKs are also regulated by related proteins called cdk inhibitors grouped into two families: the INK4 inhibitors (p16, p15, p19, and p18) and the Cip/Kip inhibitors (p21, p27, and p53). Several studies report the importance of cell-cycle proteins in the pathogenesis and the prognosis of lung cancer. This paper will review the most recent data from the literature about the regulation of cell cycle. Finally, based essentially on the data generated in our laboratory, the expression, the diagnostic, and prognostic significance of cell-cycle molecules in lung cancer will be examined.


2020 ◽  
Vol 10 ◽  
Author(s):  
Soudeh Ghafouri-Fard ◽  
Hamed Shoorei ◽  
Farhad Tondro Anamag ◽  
Mohammad Taheri

Cell cycle is regulated by a number of proteins namely cyclin-dependent kinases (CDKs) and their associated cyclins which bind with and activate CDKs in a phase specific manner. Additionally, several transcription factors (TFs) such as E2F and p53 and numerous signaling pathways regulate cell cycle progression. Recent studies have accentuated the role of long non-coding RNAs (lncRNAs) and microRNAs (miRNAs) in the regulation of cell cycle. Both lncRNAs and miRNAs interact with TFs participating in the regulation of cell cycle transition. Dysregulation of cell cycle regulatory miRNAs and lncRNAs results in human disorders particularly cancers. Understanding the role of lncRNAs, miRNAs, and TFs in the regulation of cell cycle would pave the way for design of anticancer therapies which intervene with the cell cycle progression. In the current review, we describe the role of lncRNAs and miRNAs in the regulation of cell cycle and their association with human malignancies.


2006 ◽  
Vol 114 (S 1) ◽  
Author(s):  
B Trojanowicz ◽  
Z Chen ◽  
J Bialek ◽  
Y Radestock ◽  
S Hombach-Klonisch ◽  
...  

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