Tumor suppressor genes (TSGs) elicit carcinogenic phenotypes by gene loss. In thousands of publications, however, TSGs have been assayed for activities by reintroduction into tumor cells with TSG deletions. Whereas the FHIT gene has been defined as a gene that causes programmed cell death when reintroduced to cancer cells, normal epithelial cells are FHIT+ and do not undergo signal or age-independent apoptosis. Because the FHIT gene is lost early, i.e., from premalignant bronchial epithelial cells, we determined the gene expression consequences of this event and discovered that FHIT gene inactivation increases expression of a set of proteins important in lung carcinogenesis including DNA methyltransferase 1 (Dnmt1), mitogen- activated protein kinase (Erk1) and nuclear factor Yalpha (NF-Yalpha). The mechanism of the increased mRNA and protein expression is specific stabilization of a set of normally unstable mRNAs. Moreover, increased expression of Dnmt1 is accompanied by an immediate and specific alteration in DNA methylation, which silences expression of a set of extracellularly localized tumor suppressors, including Ccn1, Ccn2 and Tgm2. Thus, our data indicate that the tumor suppressing function of Fhit involves limiting expression of oncoproteins by virtue of promoting specific mRNA decay and that Fhit loss initiates a gene expression and epigenetic cascade to promote carcinogenesis.
The specific aims of this project are: 1) To define the molecular steps by which Fhit depletion increases expression of Dnmt1 and other proteins. 2) To determine the relationship of Fhit-ApppA binding and hydrolytic activity to the function of Fhit as a regulator of expression of Dnmt1 and other proteins. 3) To define the genes that are individually and cooperatively dysregulated by loss of Fhit and gain of Dnmt1 in bronchial epithelial cells.

Public Health Relevance

Lung cancer is the leading cause of cancer deaths worldwide. The long term aim of this project is to reduce cancer incidence by exploiting the consequences of loss of the FHIT gene from bronchial epithelia. Indeed, because loss of Fhit expression leads to gain of Dnmt1 expression, this research suggests that Dnmt1 inhibition in bronchial airways may be a rational cancer chemo-preventative strategy for smokers and former smokers. Even a 10% reduction in lung cancer incidence could save more than 16,000 U.S. lives per year.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Project (R01)
Project #
5R01CA075954-15
Application #
8281595
Study Section
Special Emphasis Panel (ZRG1-BDA-M (02))
Program Officer
Knowlton, John R
Project Start
1997-08-01
Project End
2014-06-30
Budget Start
2012-07-01
Budget End
2014-06-30
Support Year
15
Fiscal Year
2012
Total Cost
$265,177
Indirect Cost
$81,760
Name
University of Iowa
Department
Biochemistry
Type
Schools of Medicine
DUNS #
062761671
City
Iowa City
State
IA
Country
United States
Zip Code
52242
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