Data from mTORC2 Signaling Drives the Development and Progression of Pancreatic Cancer

Abstract

<div>Abstract<p>mTOR signaling controls several critical cellular functions and is deregulated in many cancers, including pancreatic cancer. To date, most efforts have focused on inhibiting the mTORC1 complex. However, clinical trials of mTORC1 inhibitors in pancreatic cancer have failed, raising questions about this therapeutic approach. We employed a genetic approach to delete the obligate mTORC2 subunit <i>Rictor</i> and identified the critical times during which tumorigenesis requires mTORC2 signaling. <i>Rictor</i> deletion resulted in profoundly delayed tumorigenesis. Whereas previous studies showed most pancreatic tumors were insensitive to rapamycin, treatment with a dual mTORC1/2 inhibitor strongly suppressed tumorigenesis. In late-stage tumor-bearing mice, combined mTORC1/2 and PI3K inhibition significantly increased survival. Thus, targeting mTOR may be a potential therapeutic strategy in pancreatic cancer. <i>Cancer Res; 76(23); 6911–23. ©2016 AACR</i>.</p></div>