Synthesis of Acetogenin Analogs as Potential Therapeutics for Treating Prostate Cancer

2002 ◽  
Author(s):  
Brian L. Pagenkopf
2018 ◽  
Vol 160 ◽  
pp. 108-119 ◽  
Author(s):  
Lavinia A. Carabet ◽  
Nada Lallous ◽  
Eric Leblanc ◽  
Fuqiang Ban ◽  
Helene Morin ◽  
...  

2021 ◽  
Vol 22 (10) ◽  
pp. 5306
Author(s):  
Yingjie Shen ◽  
Hyoung Jae Lee ◽  
Rui Zhou ◽  
Hangun Kim ◽  
Gen Chen ◽  
...  

Prostate cancer (PCa) is the second most leading cause of death in males. Our previous studies have demonstrated that δ-catenin plays an important role in prostate cancer progression. However, the molecular mechanism underlying the regulation of δ-catenin has not been fully explored yet. In the present study, we found that δ-catenin could induce phosphorylation of p21Waf and stabilize p21 in the cytoplasm, thus blocking its nuclear accumulation for the first time. We also found that δ-catenin could regulate the interaction between AKT and p21, leading to phosphorylation of p21 at Thr-145 residue. Finally, EGF was found to be a key factor upstream of AKT/δ-catenin/p21 for promoting proliferation and metastasis in prostate cancer. Our findings provide new insights into molecular controls of EGF and the development of potential therapeutics targeting δ-catenin to control prostate cancer progression.


2003 ◽  
Vol 86 (7) ◽  
pp. 2671-2686 ◽  
Author(s):  
Frédéric Leroux ◽  
Tilman U. Hutschenreuter ◽  
Céline Charrière ◽  
Rosario Scopelliti ◽  
Rolf W. Hartmann

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Hui-Ming Lin ◽  
Iva Nikolic ◽  
Jessica Yang ◽  
Lesley Castillo ◽  
Niantao Deng ◽  
...  

2021 ◽  
Vol 22 (19) ◽  
pp. 10537
Author(s):  
Przemysław Hałubiec ◽  
Agnieszka Łazarczyk ◽  
Oskar Szafrański ◽  
Torsten Bohn ◽  
Joanna Dulińska-Litewka

Prostate cancer (PC) is the second most common tumor in males. The search for appropriate therapeutic options against advanced PC has been in process for several decades. Especially after cessation of the effectiveness of hormonal therapy (i.e., emergence of castration-resistant PC), PC management options have become scarce and the prognosis is poor. To overcome this stage of disease, an array of natural and synthetic substances underwent investigation. An interesting and promising class of compounds constitutes the derivatives of natural retinoids. Synthesized on the basis of the structure of retinoic acid, they present unique and remarkable properties that warrant their investigation as antitumor drugs. However, there is no up-to-date compilation that consecutively summarizes the current state of knowledge about synthetic retinoids with regard to PC. Therefore, in this review, we present the results of the experimental studies on synthetic retinoids conducted within the last decade. Our primary aim is to highlight the molecular targets of these compounds and to identify their potential promise in the treatment of PC.


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