Author/Authors :
Guertin، نويسنده , , David A. and Stevens، نويسنده , , Deanna M. and Saitoh، نويسنده , , Maki and Kinkel، نويسنده , , Stephanie and Crosby، نويسنده , , Katherine and Sheen، نويسنده , , Joon-Ho and Mullholland، نويسنده , , David J. and Magnuson، نويسنده , , Mark A. and Wu، نويسنده , , Hong and Sabatini، نويسنده , , David M.، نويسنده ,
Abstract :
Summary
omplex 2 (mTORC2) contains the mammalian target of rapamycin (mTOR) kinase and the Rictor regulatory protein and phosphorylates Akt. Whether this function of mTORC2 is critical for cancer progression is unknown. Here, we show that transformed human prostate epithelial cells lacking PTEN require mTORC2 to form tumors when injected into nude mice. Furthermore, we find that Rictor is a haploinsufficient gene and that deleting one copy protects Pten heterozygous mice from prostate cancer. Finally, we show that the development of prostate cancer caused by Pten deletion specifically in prostate epithelium requires mTORC2, but that for normal prostate epithelial cells, mTORC2 activity is nonessential. The selective requirement for mTORC2 in tumor development suggests that mTORC2 inhibitors may be of substantial clinical utility.
