Prolyl endopeptidase inhibitor Y-29794 blocks the IRS1-AKT-mTORC1 pathway and inhibits survival and in vivo tumor growth of triple-negative breast cancer

  • Cancer Biol Ther. 2020 Nov 1;21(11):1033-1040. doi: 10.1080/15384047.2020.1824989.
Ricardo E Perez  1 ,  Sarah Calhoun  1 ,  Daeun Shim  1 ,  Victor V Levenson  1 ,  Lei Duan  1 ,  Carl G Maki  1
Affiliations
  • 1. Department of Cell and Molecular Medicine, Rush University Medical Center , Chicago, IL, USA.
Abstract

Prolyl endopeptidase (PREP), also known as prolyl oligopeptidase (POP), is an enzyme that cleaves short Peptides (<30 Amino acids in length) on the C-terminal side of proline. PREP is highly expressed in multiple carcinomas and is a potential target for Cancer therapy. A potent inhibitor of PREP, Y-29794, causes long-lasting inhibition of PREP in mouse tissues. However, there are no reports on Y-29794 effects on Cancer cell and tumor proliferation. Using cell line models of aggressive Triple-Negative Breast Cancer (TNBC), we show here that Y-29794 inhibited proliferation and induced death in multiple TNBC cell lines. Cell death induced by Y-29794 coincided with inhibition of the IRS1-AKT-mTORC1 survival signaling pathway, although stable depletion of PREP alone was not sufficient to reduce IRS1-AKT-mTORC1 signaling or induce death. These results suggest that Y-29794 elicits its Cancer cell killing effect by targeting other mechanisms in addition to PREP. Importantly, Y-29794 inhibited tumor growth when tested in xenograft models of TNBC in mice. Induction of cell death in culture and inhibition of xenograft tumor growth support the potential utility of Y-29794 or its derivatives as a treatment option for TNBC Tumors.

Keywords
IRS1-AKT-mTORC1 pathway; Prolyl endopeptidase; triple-negative breast cancer.
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