Successful Targeting of an ATG7-RAF1 Gene Fusion in Anaplastic Pleomorphic Xanthoastrocytoma With Leptomeningeal Dissemination

2019 ◽  
pp. 1-7 ◽  
Author(s):  
Mehdi Touat ◽  
Nadia Younan ◽  
Philipp Euskirchen ◽  
Maxime Fontanilles ◽  
Karima Mokhtari ◽  
...  
2017 ◽  
Vol 19 (suppl_6) ◽  
pp. vi216-vi216 ◽  
Author(s):  
Alissa Thomas ◽  
Suzanne Tucker ◽  
Carl Nelson ◽  
Joshua Nickerson ◽  
Susan Durham ◽  
...  

2005 ◽  
Vol 22 (6) ◽  
pp. 614-618 ◽  
Author(s):  
Eva Passone ◽  
Stefano Pizzolitto ◽  
Serena D'Agostini ◽  
Miran Skrap ◽  
Maria Paola Gardiman ◽  
...  

2017 ◽  
Vol 134 (1) ◽  
pp. 159-162 ◽  
Author(s):  
Jason C. H. Chiang ◽  
Julie H. Harreld ◽  
Brent A. Orr ◽  
Suash Sharma ◽  
Azzam Ismail ◽  
...  

2018 ◽  
Vol 66 (1) ◽  
pp. e27465 ◽  
Author(s):  
Alissa A. Thomas ◽  
Suzanne M. Tucker ◽  
Carl J. Nelson ◽  
Joshua P. Nickerson ◽  
Susan R. Durham ◽  
...  

2019 ◽  
Vol 19 (5) ◽  
pp. 368-381 ◽  
Author(s):  
Linh N.K. Tran ◽  
Ganessan Kichenadasse ◽  
Pamela J. Sykes

Prostate cancer (PCa) is the most frequent cancer in men. The evolution from local PCa to castration-resistant PCa, an end-stage of disease, is often associated with changes in genes such as p53, androgen receptor, PTEN, and ETS gene fusion products. Evidence is accumulating that repurposing of metformin (MET) and valproic acid (VPA) either when used alone, or in combination, with another therapy, could potentially play a role in slowing down PCa progression. This review provides an overview of the application of MET and VPA, both alone and in combination with other drugs for PCa treatment, correlates the responses to these drugs with common molecular changes in PCa, and then describes the potential for combined MET and VPA as a systemic therapy for prostate cancer, based on potential interacting mechanisms.


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