Development of Bag-1L as a therapeutic target in androgen receptor-dependent prostate cancer

نویسندگان

  • Laura Cato
  • Antje Neeb
  • Adam Sharp
  • Victor Buzón
  • Scott B Ficarro
  • Linxiao Yang
  • Claudia Muhle-Goll
  • Nane C Kuznik
  • Ruth Riisnaes
  • Daniel Nava Rodrigues
  • Olivier Armant
  • Victor Gourain
  • Guillaume Adelmant
  • Emmanuel A Ntim
  • Thomas Westerling
  • David Dolling
  • Pasquale Rescigno
  • Ines Figueiredo
  • Friedrich Fauser
  • Jennifer Wu
  • Jaice T Rottenberg
  • Liubov Shatkina
  • Claudia Ester
  • Burkhard Luy
  • Holger Puchta
  • Jakob Troppmair
  • Nicole Jung
  • Stefan Bräse
  • Uwe Strähle
  • Jarrod A Marto
  • Gerd Ulrich Nienhaus
  • Bissan Al-Lazikani
  • Xavier Salvatella
  • Johann S de Bono
  • Andrew Cb Cato
  • Myles Brown
چکیده

Targeting the activation function-1 (AF-1) domain located in the N-terminus of the androgen receptor (AR) is an attractive therapeutic alternative to the current approaches to inhibit AR action in prostate cancer (PCa). Here we show that the AR AF-1 is bound by the cochaperone Bag-1L. Mutations in the AR interaction domain or loss of Bag-1L abrogate AR signaling and reduce PCa growth. Clinically, Bag-1L protein levels increase with progression to castration-resistant PCa (CRPC) and high levels of Bag-1L in primary PCa associate with a reduced clinical benefit from abiraterone when these tumors progress. Intriguingly, residues in Bag-1L important for its interaction with the AR AF-1 are within a potentially druggable pocket, implicating Bag-1L as a potential therapeutic target in PCa.

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عنوان ژورنال:

دوره 6  شماره 

صفحات  -

تاریخ انتشار 2017