Pin1 regulates the function and stability of specific phosphoproteins by catalyzing the cis/trans isomerization of peptidyl-prolyl bonds that follow phosphorylated serine or threonine residues, and is frequently overexpressed in cancer. In triple-negative breast cancer (TNBC), Pin1 mediates oncogenic signaling networks to drive the epithelial-mesenchymal transition (EMT) and cell migration, suggesting that Pin1 inhibition could address the critical need for targeted TNBC therapy. However, despite previous efforts, there are currently no Pin1 inhibitors that can serve as informative cellular probes. The goal of this research program is to develop the first covalent Pin1 inhibitors with the requisite potency, selectivity, and cell permeability to interrogate the potential of Pin1 as a therapeutic target in TNBC.
The first aim i s to synthesize linear and macrocyclic peptidomimetic inhibitors of Pin1 that act via the formation of a covalent adduct with a critical cysteine residue, Cys113, in the Pin1 active site. Such covalent inhibitors would overcome the limitations of existing Pin1 inhibitors by achieving added specificity and longer lasting biochemical effects. In the second aim, these inhibitors will be characterized with respect to their cellular target engagement, anti-proliferative effects, and effects on EMT and cell migration in TNBC. This proposal therefore offers the first Pin1 inhibitors with the required selectivity and potency to be used as cellular probes to study Pin1 biology, and contributes to the growing body of evidence for Pin1 inhibition as a treatment option for TNBC.

Public Health Relevance

The peptidyl-prolyl isomerase, Pin1, regulates the structure and activity of specific proteins by isomerizing phosphorylated Ser/Thr-Pro bonds. Pin1 is frequently overexpressed in triple-negative breast cancer (TNBC) and promotes cell transformation by stabilizing oncogenes and inactivating tumor suppressors, as well as by driving the epithelial-mesenchymal transition (EMT). This proposal has important public health applications because it offers the first potent, selective, and cell permeable covalent Pin1 inhibitors, which will not only serve as useful tool compounds with which to study Pin1 biology, but also will inform the design of future targeted therapies for TNBC.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
1F31CA225066-01
Application #
9469682
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Schmidt, Michael K
Project Start
2018-04-01
Project End
2020-03-31
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
Harvard University
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
082359691
City
Cambridge
State
MA
Country
United States
Zip Code