Aerodigestive tract tumors have been hypothesized to represent a """"""""field cancerization"""""""" process whereby a whole field is exposed to carcinogenic insult, accumulates genetic damage, and is at increased risk for proceeding through a multistep process of tumor development. The purpose of this proposal is to examine the hypothesis of """"""""field cancerization"""""""" at the cellular and molecular levels to identify probes which can be used to characterize the multistep tumorigenesis process in the aerodigestive tract. The information gained from these initial studies will then be utilized to assess risk of malignancy in the aerodigestive tract (in individuals at risk for tumor development) as well as to determine the effect of chemoproventive treatment on these cellular parameters. Using surgically resected tumor and normal tissue obtained from individuals with primary head and neck tumors and premalignant lesions (leukoplakia), we propose to identify cytogenetic, immunocytochemical, and molecular markers that can be utilized to identify genotypic and phenotypic changes associated with tumorigenesis. We will then examine adjacent and distant """"""""normal"""""""" tissue, in and out of the field at risk, for the degree of genetic alteration as well as for the degree of dysregulation of proliferation and differentiation (i.e. characterization of the field). Hypothetically, one would expect that individuals with head and neck primaries who exhibit increased genetic and phenotypic alterations in their normal tissue would be at increased risk for the development of a second primary. Similarly, those individuals exhibiting increased alterations in premalignant tissue (e.g. leukoplakia) might be expected to be at increased risk for developing oral cancer. These hypotheses will be tested first in a retrospective fashion by examining archival tumor and normal tissue specimens of individuals previously resected for primary head and neck tumors who have or have not subsequently developed a second primary. During the fourth and fifth years, the informative immunocytochemical and molecular probes will be utilized to examine tissues obtained prospectively from patients entered at M.D. Anderson Cancer Center onto the clinical protocols described in Projects 1 and 3 to determine the validity of the findings obtained from retrospective studies as well as to determine the effect of chemopreventive treatment on the expression of these markers in the tissue at risk.

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Research Program Projects (P01)
Project #
5P01CA052051-08
Application #
6102605
Study Section
Project Start
1998-12-01
Project End
1999-11-30
Budget Start
1998-10-01
Budget End
1999-09-30
Support Year
8
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Texas MD Anderson Cancer Center
Department
Type
DUNS #
001910777
City
Houston
State
TX
Country
United States
Zip Code
77030
Hildebrandt, Michelle A T; Lippman, Scott M; Etzel, Carol J et al. (2012) Genetic variants in the PI3K/PTEN/AKT/mTOR pathway predict head and neck cancer patient second primary tumor/recurrence risk and response to retinoid chemoprevention. Clin Cancer Res 18:3705-13
Lee, J Jack; Wu, Xifeng; Hildebrandt, Michelle A T et al. (2011) Global assessment of genetic variation influencing response to retinoid chemoprevention in head and neck cancer patients. Cancer Prev Res (Phila) 4:185-93
Wang, Jianming; Lippman, Scott M; Lee, J Jack et al. (2010) Genetic variations in regulator of G-protein signaling genes as susceptibility loci for second primary tumor/recurrence in head and neck squamous cell carcinoma. Carcinogenesis 31:1755-61
Zhang, Xiaofan; Yang, Hushan; Lee, J Jack et al. (2010) MicroRNA-related genetic variations as predictors for risk of second primary tumor and/or recurrence in patients with early-stage head and neck cancer. Carcinogenesis 31:2118-23
Wu, Xifeng; Spitz, Margaret R; Lee, J Jack et al. (2009) Novel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of genetic variants. Cancer Prev Res (Phila) 2:617-24
William Jr, William N; Lee, J Jack; Lippman, Scott M et al. (2009) High-dose fenretinide in oral leukoplakia. Cancer Prev Res (Phila) 2:22-6
Papadimitrakopoulou, Vassiliki A; Lee, J Jack; William Jr, William N et al. (2009) Randomized trial of 13-cis retinoic acid compared with retinyl palmitate with or without beta-carotene in oral premalignancy. J Clin Oncol 27:599-604
Kawaguchi, Hidetoshi; El-Naggar, Adel K; Papadimitrakopoulou, Vali et al. (2008) Podoplanin: a novel marker for oral cancer risk in patients with oral premalignancy. J Clin Oncol 26:354-60
Wu, Xifeng; Gu, Jian; Dong, Qiong et al. (2006) Joint effect of mutagen sensitivity and insulin-like growth factors in predicting the risk of developing secondary primary tumors and tumor recurrence in patients with head and neck cancer. Clin Cancer Res 12:7194-201
Lippman, Scott M; Lee, J Jack (2006) Reducing the ""risk"" of chemoprevention: defining and targeting high risk--2005 AACR Cancer Research and Prevention Foundation Award Lecture. Cancer Res 66:2893-903

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