Head and neck cancers affect 40,000 individuals each year, accounting for 6% of malignancies. Radiation therapy, a mainstay of treatment, often causes irreversible damage to the salivary glands resulting in permanent xerostomia or dry mouth. These patients are at risk for oral and systemic infection and also experience significantly diminished quality of life. Our current treatments are only palliative (e.g. artificil saliva / chewing gum) and do not address the underlying pathology. Recent results from our laboratory have demonstrated therapeutic efficacy of nanoparticle (NP) mediated siRNA delivery to irradiated salivary tissue in a preclinical murine model. This transiently modulates th cellular response to radiation to favor survival. What remains unclear, however, is long term viability of this and other radioprotective strategies, particularly in evaluating the potential fo cellular quiescence or the risk of secondary malignancy. To investigate long term fate of radioprotected tissue, a needed step towards clinical translation, we are developing a nanoparticle system to co-deliver siRNA and an active estrogen agonist (Aim 1). This agent, 4-hydroxytamoxifen (4-OHT), when delivered to the appropriate transgenic tissues, will induce expression of a fluorescent reporter protein that will persist in treated cells and daughter cells beyond the transient effect of siRNA. Additionally, because the majority of radiation damage to biological tissues is from reactive oxygen species (ROS), we are interested in dampening the initial radiation insult. The only FDA-approved xerostomia prophylactic agent is amifostine, an intravenously administered radical scavenger, with a narrow therapeutic window, and the potential for systemic side effects including tumor protection. Our proposed strategy is to locally pre-treat the gland with a novel nanoparticle formulation aimed at arming salivary tissues with an antioxidant supply via the sustained intracellular release of active amifostine (Aim 2). Completion of these aims will identify targets and sequellae of radioprotection, while simultaneously determining which of the two therapeutic strategies is more effective. Also detailed within this application are clinical activities to complement the research training of the applicant. Both sponsors are committed to the applicant's development as a clinician-scientist and will continue to train the applicant in experimental design, scientific writing, and presentation. The applicant will also pursue four longitudinal clinical experiences with physicians working in cancer treatment to gain a better understanding of the clinical context of his research. Finally, the applicant will continue involvement in the development of future experimental studies during his medical training.

Public Health Relevance

Impact Head and neck cancers comprise 6% of malignancies diagnoses annually, affecting approximately 40,000 patients, who will then go on to receive radiotherapy. Radiation-induced xerostomia carries a significant risk for subsequent life threatening pathology and profoundly diminished quality of life for patients by interfering with their ability to eat and sleep. We propose novel nanoparticle platforms for radioprotection via localized, controlled delivery of siRNA and antioxidant therapies, which have the potential to prevent xerostomia altogether for our patients.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Individual Predoctoral NRSA for M.D./Ph.D. Fellowships (ADAMHA) (F30)
Project #
5F30CA206296-02
Application #
9275242
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Damico, Mark W
Project Start
2016-05-01
Project End
2020-04-30
Budget Start
2017-05-01
Budget End
2018-04-30
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
University of Rochester
Department
Biomedical Engineering
Type
Biomed Engr/Col Engr/Engr Sta
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Varghese, Jomy J; Schmale, Isaac L; Hansen, Mollie Eva et al. (2018) Murine Salivary Functional Assessment via Pilocarpine Stimulation Following Fractionated Radiation. J Vis Exp :
Varghese, J J; Schmale, I L; Mickelsen, D et al. (2018) Localized Delivery of Amifostine Enhances Salivary Gland Radioprotection. J Dent Res 97:1252-1259
Varghese, Jomy J; Schmale, Isaac L; Wang, Yuchen et al. (2018) Retroductal Nanoparticle Injection to the Murine Submandibular Gland. J Vis Exp :
Malcolm, Dominic W; Varghese, Jomy J; Sorrells, Janet E et al. (2018) The Effects of Biological Fluids on Colloidal Stability and siRNA Delivery of a pH-Responsive Micellar Nanoparticle Delivery System. ACS Nano 12:187-197