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  Vol. 124 No. 8, August 1998 TABLE OF CONTENTS
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Malignancy Detection by Molecular Cytogenetics in Clinically Normal Mucosa Adjacent to Head and Neck Tumors

José E. Barrera, MD; Hong Ai, DDS; Zhaoxing Pan, MS; Arlen D. Meyers, MD; Marileila Varella-Garcia, PhD

Arch Otolaryngol Head Neck Surg. 1998;124:847-851.

Objective  To identify the potential use of chromosome imbalances as biomarkers for tumorigenesis in head and neck squamous cell carcinoma (HNSCC) by fluorescence in situ hybridization (FISH).

Design  In this case-control study, chromosome copy numbers were assessed in dual-target, dual-color FISH assays using DNA probes specific for 14 human chromosomes (1, 2, 3, 6, 7, 8, 9, 10, 11, 12, 15, 17, X, and Y) applied to exfoliated epithelial cells.

Setting  University medical center.

Patients  We examined 20 cell brushings (from 10 primary tumors and 10 clinically normal margins) collected from 10 patients with HNSCC and compared these with cell brushings from the oral cavity of 10 nonsmoker and 10 smoker control subjects.

Intervention  None.

Main Outcome Measure  Chromosomal aneuploidy.

Results  Specimens from nonsmokers displayed greater than 91% of cells with normal signals, indicating high analytical sensitivity for the probes. Specimens from smokers demonstrated large variability without significant imbalance (P>.05) compared with those from nonsmokers. Tumor specimens from patients with HNSCC displayed significant chromosomal imbalance (P<.05) for all probes except chromosome Y. Similar imbalance, although in lower frequency, was found in all clinically normal adjacent mucosa specimens.

Conclusions  Interphase FISH demonstrated great applicability in detecting chromosome imbalance associated with malignancy in HNSCC and clinically normal adjacent cells, thereby detecting subclinical tumorigenesis. A panel of chromosome probes (chromosomes 3, 8, 9, and 10) is proposed as an efficient and sensitive additional tool for future routine screening of tumor margins and potential diagnosis of residual disease in HNSCC.


From the Department of Otolaryngology–Head and Neck Surgery (Drs Barrera and Meyers), Department of Medicine, Division of Medical Oncology (Drs Ai and Varella-Garcia), and Department of Preventive Medicine (Mr Pan), University of Colorado Health Sciences Center, Denver.


RELATED ARTICLE

"Molecular Margins": A Better Measure?
Margaret Brandwein and David Yong Zhang
Arch Otolaryngol Head Neck Surg. 1998;124(8):841-842.
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THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Smoking and smokeless tobacco-associated human buccal cell mutations and their association with oral cancer--a review.
Proia et al.
Cancer Epidemiol. Biomarkers Prev. 2006;15:1061-1077.
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Molecular Cytogenetics in Solid Tumors: Laboratorial Tool for Diagnosis, Prognosis, and Therapy
Varella-Garcia
The Oncologist 2003;8:45-58.
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Chromosomal Aneuploidy as a Predictor for Poor Outcome in Patients With Head and Neck Cancer
Barrera and Varella-Garcia
Arch Otolaryngol Head Neck Surg 2001;127:1519-1520.
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"Molecular Margins": A Better Measure?
Brandwein and Zhang
Arch Otolaryngol Head Neck Surg 1998;124:841-842.
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