The goal of this proposal is to increase our understanding of the therapeutic benefits of using platelets for preventing the spread of cancer, or metastasis. Metastasis is the main cause of cancer-associated mortality that occurs when some cancer cells, also called circulating tumor cells (CTCs), detach from primary tumor sites and enter the bloodstream to invade other tissues and organs at different locations. The presence of CTCs in patients is associated with a poor prognosis because once CTCs enter the bloodstream it is difficult to prevent them from reaching secondary organs and spreading cancer. Therefore, targeting CTCs may represent a promising target for anticancer therapies. Once CTCs enter into the bloodstream, they face many survival challenges including immunological attack, shear forces, and apoptosis. To enhance their survival rate, CTCs strongly attract platelets to form a protective cloak that helps the cancer cells survive the forces in the bloodstream and to escape immune surveillance. Although the mechanisms by which platelets interact with circulating tumor cells are poorly understood, studies have shown that they are involved in cancer progress, especially during metastasis where platelets help to degrade extracellular matrix (ECM) to support the colonization of cancer cells in distant locations from the original tumor formation site. We propose to take advantage of platelets' innate association with circulating tumor cells and their storage, trafficking, and release capacities of small molecules, to engineer them as delivery vehicles for the development of next generation delivery methods for targeting and destroying CTCs to prevent or minimize metastasis.

Public Health Relevance

Metastasis is the main cause of cancer-associated mortality. Developing novel cell therapies that are capable of targeting and destroying circulating cancer cells would significantly improve human health. We will engineer platelets to seek and destroy cancer cells in the bloodstream before they invade other tissues and spread disease.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
NIH Director’s New Innovator Awards (DP2)
Project #
1DP2CA250006-01
Application #
9782048
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Watson, Joanna M
Project Start
2019-09-20
Project End
2024-06-30
Budget Start
2019-09-20
Budget End
2024-06-30
Support Year
1
Fiscal Year
2019
Total Cost
Indirect Cost
Name
University of Utah
Department
Biomedical Engineering
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112