Accession Number:



Targeting the UPR to Circumvent Endocrine Resistance in Breast Cancer

Personal Author(s):

Corporate Author:

Georgetown University Washington United States

Report Date:



In this Idea Expansion IDEX Grant, we propose that targeting IRE1 in endocrine resistant breast cancer cells with N-4-Phenoxy-phenyl-2-5-pyridin-3-yl-2H-1,2,4triazol-3-ylsulfanyl-acetamide NPPTA lead compound, or its analogs, will block pro-survival signaling from the UPR and prevent survival via pro-survival autophagy and an inhibition of apoptosis. We hypothesize that these effects will be mediated in part by the inhibition of XBP1 splicing and its ability to regulate BCL2 family members and NFB. Furthermore, a combination of NPPTA and AEs will interact synergistically to selectively kill AE resistant breast cancer cells in vitro and in vivo.

Descriptive Note:

Technical Report,15 Sep 2013,14 Sep 2016



Communities Of Interest:

Distribution Statement:

Approved For Public Release;

File Size: