Melanoma is one of the few cancers, both early and late stages that has increased in incidence over the last few decades. The poor survival of patients with advanced or metastatic melanoma reflects its aggressive nature and the ineffectiveness of current treatment and prevention strategies. Chemoprevention represents a rational alternative to combat this deadly cancer by preventing, delaying or reversing the malignant transformation of a melanocyte. Demonstrating efficacy of any preventive intervention requires long-term, randomized clinical trials involving large populations. Such studies are logistically and financially difficult to perform with a tremendous investment of time and resources. The central hypotheses of this proposal are that a human model for melanoma Chemoprevention studying patients with dysplastic nevi can be used to test putative Chemoprevention agents by modulating important molecular events and that topical curcumin can delay or prevent transformation and progression of melanocytes in humans at least in part by its modulating effects on nuclear factor kappa B (NF-kB) and 12-lipoxygenase (12-LOX). In order to test these hypotheses the following four specific aims are proposed: (1) determine the proportion of patients with dysplastic nevi in the University of Michigan Multidisciplinary Melanoma Clinic who will participate in a prospective clinical trial requiring serial skin biopsies;(2) define the intra- and inter-lesional histopathologic and biomarker variability of nuclear factor kappa B (NF-kB) activation, 12-lipoxygenase (12-LOX), and prostaglandin E2 (PGE2) expression in normal skin, benign nevi, and dysplastic nevi;(3) define the absorption, safety, tolerability, and optimal dose concentration of topical curcumin;and (4) determine if topical curcumin can significantly alter the expression of nuclear factor kappa B (NF-kB) activation, 12- lipoxygenase (12-LOX), and downstream markers (Ki-67) in pigmented skin cells. The proposed studies will demonstrate that we can recruit sufficient patients for putative chemopreventive agents, that topical curcumin is safe and tolerable, and that curcumin modulates 12-LOX expression and NF-kB release in human skin. This line of investigation will help determine the importance of NF-kB and 12-LOX in melanoma carcinogenesis and provide an infrastructure for rapid testing of putative Chemoprevention agents and biomarkers in the future.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Academic/Teacher Award (ATA) (K07)
Project #
5K07CA111653-05
Application #
7922568
Study Section
Subcommittee G - Education (NCI)
Program Officer
Perkins, Susan N
Project Start
2006-09-19
Project End
2012-05-31
Budget Start
2010-09-01
Budget End
2012-05-31
Support Year
5
Fiscal Year
2010
Total Cost
$137,700
Indirect Cost
Name
University of Michigan Ann Arbor
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
073133571
City
Ann Arbor
State
MI
Country
United States
Zip Code
48109
Cha, Hyuk C; Harting, Mandy; Cha, Kelly B et al. (2012) Effects of contiguous scars in dermatoscopic evaluation of clinically atypical melanocytic nevi. J Am Acad Dermatol 66:e179-80
Lao, Christopher D; Johnson, Timothy; Sondak, Vernon K et al. (2011) Feasibility of serial biopsies of large dysplastic nevi as a melanoma chemoprevention model. J Am Acad Dermatol 64:1188-90