Nucleotide-based drugs, such as antisense (ASO), represent an essential class of drug types that are particularly useful for those so-called ?undruggable? targets by small molecules and antibodies. However, one of the biggest hurdles in the translation of ASO drugs is the poor in vivo delivery. Several barriers exist to prevent ASOs from efficiently reaching their target cells in vivo: rapid renal clearance, nuclease degradation, unspecific absorption, low efficiency to penetrate across the endothelium and spread in extravascular tissue. In this proposal, I aim to apply the technologies of peptide targeting and nanomaterial to enhance the delivery efficiency of ASOs into solid tumors. To prevent renal filtration and nuclease degradation, ASOs will be encapsulated within porous silicon nanoparticles (pSiNPs). pSiNPs are biodegradable and have low or no toxicity in vivo. More importantly, pSiNPs have likely the highest loading efficiency for ASOs and other oligonucleotides. The most important goal of our proposal is to help ASOs preferentially accumulate in tumors, and penetrate across tumor vessels to access to those target cells far away from the circulation. Our tumor-penetrating CendR peptides are one of the few tools available to achieve this goal. By engaging with certain receptor on the tumor vessels, CendR peptides activate an active transport process across tumor vessels along with a wide range of cargo types, including pSiNPs. In the Aim 1, I will synthesize CendR-functionalized, ASO-loaded pSiNPs. Besides chemical characterization, I will also validate the cell entry and gene-silencing efficacy of this system in vitro. In the Aim 2, I will evaluate the in vivo toxicity, pharmacokinetics and tissue distribution. In the Aim 3, the gene modulation and tumor-inhibitory efficacy of CendR-pSiNP-ASO will be determined using animal tumor models. My proposed studies hold great potential for improving the tumor delivery and antitumor efficacy of ASOs, and accelerating the transition of prototype ASO drugs into the clinic.

Public Health Relevance

Antisense molecules, composed of small strands of nucleotides, represent an important drug type that provides us almost unlimited power to eliminate disease-causing genes. However, the transition from the prototypes to marketed drugs has been slow, largely due to the low efficiency of delivering these molecules to their sites of action inside the body. Here we propose to combine the technologies of active targeting and nanomaterial to ?navigate? more antisense drugs into solid tumors, which holds the promise to boosting up their antitumor efficacy and accelerating the transition into the clinic.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
1R01CA214550-01
Application #
9289598
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Mckee, Tawnya C
Project Start
2017-09-14
Project End
2017-12-28
Budget Start
2017-09-14
Budget End
2017-12-28
Support Year
1
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Sanford Burnham Prebys Medical Discovery Institute
Department
Type
DUNS #
020520466
City
La Jolla
State
CA
Country
United States
Zip Code
92037