Skip to main content
Grant Details

Grant Number: 5R01CA072030-04 Interpret this number
Primary Investigator: Farrow, Diana
Organization: Fred Hutchinson Cancer Research Center
Project Title: Mutagen Sensitivity & Progression in Barretts Esophagus
Fiscal Year: 1999
Back to top


Abstract

DESCRIPTION: (Adapted from the Applicant's Abstract): Barretts esophagus is a metaplastic condition that occurs in 10-20% of persons with chronic gastroesophageal reflux. Persons with this condition are at high risk, estimated at 1-2% per year, of developing esophageal adenocarcinoma, a cancer that is increasing rapidly in incidence. This proposal builds upon an ongoing cohort study of persons with Barrett's metaplasia that is designed to identify cell cycle and genetic abnormalities that predict risk of developing high grade dysplasia or adenocarcinoma, and to use these biomarkers as intermediate endpoints in epidemiologic studies. The overall goal of the proposed study is to determine whether chromosomal instability, as measured in vitro in cultured lymphocytes by the bleomycin sensitivity assay, or in vivo as allelic losses on specific chromosomes, predicts neoplastic progression among patients (N=335) with Barrett s esophagus. Specific aims are to test the hypothesis that 1) bleomycin-sensitive persons are at increased risk of histologic progression to high grade dysplasia or cancer, or of developing validated intermediate endpoints including aneuploidy or elevated G2 fractions; and 2) patients in whom allelic losses are observed on chromosomes 1p, 5q, 9p, 13q, or 18q in esophageal biopsies are at increased risk of neoplastic progression as defined above. In the third aim, cross-sectional analyses of baseline blood samples and biopsy tissue will test the hypothesis that sensitivity to bleomycin-induced chromosomal damage in vitro predicts chromosomal instability in vivo as evidenced by allelic losses. The ongoing study will provide biopsies and blood samples, along with data on major risk factors for esophageal adenocarcinoma for assessment of confounding and effect modification. Allelic losses in biopsy tissue will be identified by whole genome amplification and PCR using multiple polymorphic markers. This study will validate a proposed marker of cancer susceptibility in a prospective study of high risk persons; test a mechanism by which mutagen sensitivity may affect cancer risk; and further understanding of the genetic events leading to the development of esophageal adenocarcinoma, which serves as a model system for other human cancers.

Back to top


Publications

Mutagen sensitivity and neoplastic progression in patients with Barrett's esophagus: a prospective analysis.
Authors: Chao D.L. , Maley C.C. , Wu X. , Farrow D.C. , Galipeau P.C. , Sanchez C.A. , Paulson T.G. , Rabinovitch P.S. , Reid B.J. , Spitz M.R. , et al. .
Source: Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2006 Oct; 15(10), p. 1935-40.
PMID: 17035402
Related Citations

Over-expression of gastrin-releasing peptide in human esophageal squamous cell carcinomas.
Authors: Fang M.Z. , Liu C. , Song Y. , Yang G.Y. , Nie Y. , Liao J. , Zhao X. , Shimada Y. , Wang L.D. , Yang C.S. .
Source: Carcinogenesis, 2004 Jun; 25(6), p. 865-71.
EPub date: 2004-02-04.
PMID: 14764456
Related Citations

Detection of multiple gene hypermethylation in the development of esophageal squamous cell carcinoma.
Authors: Nie Y. , Liao J. , Zhao X. , Song Y. , Yang G.Y. , Wang L.D. , Yang C.S. .
Source: Carcinogenesis, 2002 Oct; 23(10), p. 1713-20.
PMID: 12376481
Related Citations

DNA hypermethylation is a mechanism for loss of expression of the HLA class I genes in human esophageal squamous cell carcinomas.
Authors: Nie Y. , Yang G. , Song Y. , Zhao X. , So C. , Liao J. , Wang L.D. , Yang C.S. .
Source: Carcinogenesis, 2001 Oct; 22(10), p. 1615-23.
PMID: 11577000
Related Citations

Clonal expansion and loss of heterozygosity at chromosomes 9p and 17p in premalignant esophageal (Barrett's) tissue.
Authors: Galipeau P.C. , Prevo L.J. , Sanchez C.A. , Longton G.M. , Reid B.J. .
Source: Journal of the National Cancer Institute, 1999-12-15; 91(24), p. 2087-95.
PMID: 10601379
Related Citations

Mechanisms of inactivation of p14ARF, p15INK4b, and p16INK4a genes in human esophageal squamous cell carcinoma.
Authors: Xing E.P. , Nie Y. , Song Y. , Yang G.Y. , Cai Y.C. , Wang L.D. , Yang C.S. .
Source: Clinical cancer research : an official journal of the American Association for Cancer Research, 1999 Oct; 5(10), p. 2704-13.
PMID: 10537333
Related Citations

Loss of heterozygosity of the Rb gene correlates with pRb protein expression and associates with p53 alteration in human esophageal cancer.
Authors: Xing E.P. , Yang G.Y. , Wang L.D. , Shi S.T. , Yang C.S. .
Source: Clinical cancer research : an official journal of the American Association for Cancer Research, 1999 May; 5(5), p. 1231-40.
PMID: 10353761
Related Citations




Back to Top