Targeted Core Shell Nanogels for Triple Negative Breast Cancer The central goal of this project is to improve systemic therapies of cancer using soft nanomaterials that can deeply penetrate into tumors and deliver potent anticancer agents to targeted cancer cells. Many small-molecule therapeutics that were highly promising for cancer therapy, eventually failed clinical translation due to toxicity, poor solubility, stability and othr delivery related problems. Recent advances in nanoparticle drug carriers provide a unique opportunity to "rescue" these agents and enable their clinical application. This is the focal point of our research using nanocarriers that can incorporate such agents, and preferentially deliver them to tumors. Our group has successfully developed a novel platform for drug delivery that uses aqueous polymeric gel nanoparticles, core-shell nanogels (CSNGs). CSNGs are manufactured through a proprietary self-assembly process and can be readily filled with various drug payloads. They are water-swollen and are practically non- adhesive, which may diminish their off-target side effects. We hypothesize that (a) the systemic and tumor flow dynamics of CSNGs will be a function of their molecular architecture and mechanical properties (b) and that these properties can be rationally controlled to modify the PK, distribution and tumor penetration of the CSNGs and the drugs they deliver. We will focus our research efforts on using CSNGs in the triple negative breast cancer (TNBC), a disease that despite treatment advances, still has a very poor outcome. As targeting strategies we will use the novel single-domain polypeptide antagonists of the EGFR and HER3 that are frequently overexpressed in TNBC and are associated with higher risk of mortality in TNBC. We assembled a cross- disciplinary team of physician-scientists and experts in nanotechnology, pharmacology and chemoinformatics, and will focus our research efforts on using POx micelle therapeutics in TNBC, a disease that despite treatment advances has a very poor outcome.
The specific aims are: 1. Determine how the molecular architecture and mechanical properties of polypeptide-based CSNGs affects their ability to load, deliver and release therapeutic cargos. 2. Determine how the structure and mechanical properties of the drug-loaded CSNGs affect the in vivo PK and tumor distribution of the drugs and nanogels in murine models of TNBC. 3. Develop EGFR and HER3 targeted drug-loaded CSNGs with maximal tumor penetration, maximal delivery of drug payload to tumors and potent anti-tumor activity in TNBC These integrative efforts allow to address major barriers in developing novel nanotechnology platforms for the treatment of TNBC, and facilitate our understanding of the cancer biology and the mechanisms of in vivo delivery. If successful, we will determine a new targeted formulation of chemotherapeutic drugs in CSNGs that may be highly effective in treatment of TNBC. The results will then be reviewed with our clinical advisors for further consideration of these formulations for translational and clinical development.

Public Health Relevance

The proposed research focuses on an innovative targeting strategy to treat triple negative breast cancer (TNBC) that despite treatment advances has a very poor outcome;we will use biodegradable nanogels that carry potent chemotherapeutic agents and are decorated with novel polypeptide antagonists to EFGR and HER3 receptors displayed in the TNBC. The softness of the nanogels is adjusted in an attempt to maximize the penetration of the nanogels deeply into tumor, which is one of the major barriers to targeted nanotherapeutics, and such soft targeted nanogels can deliver and release their therapeutic cargo to the TNBC tumors. The polypeptide antagonists of the receptors attached to nanogels act in concert with the delivered drugs and inhibit downstream signaling pathways to produce most potent therapeutic effect on the TNBC.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project--Cooperative Agreements (U01)
Project #
1U01CA198910-01
Application #
8959834
Study Section
Special Emphasis Panel (ZCA1-TCRB-9 (M1))
Program Officer
Morris, Stephanie A
Project Start
2015-08-14
Project End
2020-07-31
Budget Start
2015-08-14
Budget End
2016-07-31
Support Year
1
Fiscal Year
2015
Total Cost
$494,617
Indirect Cost
$130,002
Name
University of North Carolina Chapel Hill
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
608195277
City
Chapel Hill
State
NC
Country
United States
Zip Code
27599