The long term goal of this research is to develop clinically relevant multimodal MSN-based therapeutic strategies with the ability of overcoming chemo and stromal resistance to improve the final outcome of pancreatic ductal adenocarcinoma (PDAC) treatment. PDAC is the fourth leading cause of cancer death in the United States. This is one of the most difficult conditions to treat, with a 5-year survival at abot 6%. The horrific prognosis of PDAC is a result of late diagnosis and the tumor's refractory behavior toward current drug treatment. Mesoporous silica nanoparticles (MSNs) hold considerable promise as the next generation of nanomedicine that enables the early detection of disease, simultaneous monitoring and treatment, and targeted therapy with minimal toxicity. The hypothesis underlying this proposal is that by using MSNs as scaffold, we can combine different therapies such as chemotherapy, targeted therapy and combination therapy to overcome some of the main deficiencies in the current treatment of PDAC. The main target of this proposal is to develop multimodal MSN-based therapeutic strategies with the ability of overcoming chemo and stromal resistance to improve the final outcome of PDAC treatment. This goal will be accomplished by completion of three Specific Aims: 1) To develop novel MSN-based approaches for combinatorial chemotherapy and targeted therapy of PDAC; 2) To evaluate the in vivo biodistribution, pharmacokinetics, targeting ability and therapeutic efficacy of MSN materials developed in Aim 1; and 3) To develop MSN-based delivery platforms that combine chemotherapy and targeted therapy with stromal-depleting agents as novel strategies to improve PDAC treatment. The results of this work will lead to the development of several platforms with the ability of overcoming chemo and stromal resistance to improve the treatment of PDAC. Moreover; the in vivo results, obtained from a unique triplet transgenic PDAC mouse model, will provide the proof of concept to justify the evaluation of these platforms in clinical studies. These advancements in PDAC treatment will eventually impact the clinical care of this deadly disease.

Public Health Relevance

The proposed research is relevant to public health because pancreatic cancer is the fourth leading cause of cancer death in the USA. Although some progress has been made in developing novel targeted therapies, the overall survival rate has not improved in the last decade. In this work, we develop and evaluate nanoparticle-based combinatorial therapies that overcome chemo and stromal resistance to improve the final outcome of pancreatic cancer treatment.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15CA192160-01
Application #
8812549
Study Section
Nanotechnology Study Section (NANO)
Program Officer
Fu, Yali
Project Start
2014-12-23
Project End
2017-12-22
Budget Start
2014-12-23
Budget End
2017-12-22
Support Year
1
Fiscal Year
2015
Total Cost
$437,210
Indirect Cost
$139,889
Name
University of North Carolina Charlotte
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
066300096
City
Charlotte
State
NC
Country
United States
Zip Code
28223
Dréau, Didier; Moore, Laura Jeffords; Alvarez-Berrios, Merlis P et al. (2016) Mucin-1-Antibody-Conjugated Mesoporous Silica Nanoparticles for Selective Breast Cancer Detection in a Mucin-1 Transgenic Murine Mouse Model. J Biomed Nanotechnol 12:2172-2184
Alvarez-Berríos, Merlis P; Vivero-Escoto, Juan L (2016) In vitro evaluation of folic acid-conjugated redox-responsive mesoporous silica nanoparticles for the delivery of cisplatin. Int J Nanomedicine 11:6251-6265
Walker, William A; Tarannum, Mubin; Vivero-Escoto, Juan L (2016) Cellular Endocytosis and Trafficking of Cholera Toxin B-Modified Mesoporous Silica Nanoparticles. J Mater Chem B 4:1254-1262