Background: Lung cancer chemoprevention is an important concept to reduce lung cancer incidence and thus lung cancer related mortality. Most chemoprevention approaches so far have either resulted in negative or even harmful results. The role of epigenetic alterations in non-small cell lung cancer is well established. We have exciting preliminary data that lung cancer risk is substantially decreased in US veterans with long term use of the HDAC-Inhibitor valproate compared to controls which were matched by age and diagnosis (HR 0.63;95%CI 0.51-0.74). In addition, we have in-vitro data that valproate has far further reaching epigenetic effects than merely upregulation of acetylated histones. Specifically, we also observe induction of the H3K4m2- 3 activating histone mark and downregulation of the DNAmethyltransferase (DNMT1) and the histone H3K9 methyltransferase G9A, together with a reduction in anchorage independent colony formation in soft-agar. We hypothesize that due to its direct and indirect epigenetic effects valproate can a) permanently reverse and b) prevent oncogenic transformation in bronchial epithelial cells. The study has three specific aims: #1: To determine the underlying mechanisms of HDAC-I mediated prevention and reversal of bronchial epithelial cell transformation and to study associated changes in histone modifications at individual gene levels #2: To determine the effects of HDAC-inhibition on genome-wide patterns of DNA methylation and H3K9me3- marks in carcinogen transformed cells. #3: To determine if HDAC-I exposure can reverse DNA methylation in the sputum of high-risk subjects for lung cancer Significance: Should HDAC inhibition, as hypothesized, truly permanently reverse oncogenic transformation, this will be a major milestone, since no other chemopreventive strategy has been show to have that effect so far. In this case, valproate would in fact be an ideal chemopreventive agent since it would allow to reset the "epigenetic clock" to a pre-transformed phenotype and it would alleviate the need for patients at risk to stay on life-long therapy. Preliminary data of our population study in US veterans strongly supports HDAC inhibition as a clinically active chemoprevention strategy in lung cancer. With a 37% absolute risk reduction for lung cancer incidence, this would translate into 55,000 lives saved per year.

Public Health Relevance

US veterans are at particularly high risk for lung cancer, mostly due to tobacco- and service related toxin exposure such as asbestos and agent orange. Therefore a study that could reduce this risk is of particular importance to the VA. We have exciting preliminary data that lung cancer risk may be substantially decreased in US veterans with long term use of the HDAC-Inhibitor valproate (HR 0.63;95% CI 0.51-0.74). Given 210,000 new lung cancers per year, this 37% risk reduction for the development of lung cancer could result in the prevention of 77,700 new lung cancer cases and about 55,000 deaths a year. We have cell-culture evidence that valproate exposure reverses epigenetic gene silencing of certain tumor suppressor genes and that it induces epigenetic changes that reach far beyond the expected mere increase in histone acetylation. We will test the hypothesis that HDAC-inhibition permanently reverses and prevents oncogenic transformation and determine the underlying molecular mechanisms.

Agency
National Institute of Health (NIH)
Institute
Veterans Affairs (VA)
Type
Veterans Administration (IK2)
Project #
5IK2BX001283-03
Application #
8601405
Study Section
Oncology A (ONCA)
Project Start
2012-01-01
Project End
2016-12-31
Budget Start
2014-01-01
Budget End
2014-12-31
Support Year
3
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Veterans Health Administration
Department
Type
DUNS #
824835805
City
Decatur
State
GA
Country
United States
Zip Code
30033