The flow cytometric analysis of premalignant and malignant lesions in head and neck squamous cell carcinoma

被引:24
作者
Abou-Elhamd, Kamal-Eldin Ahmed [1 ]
Habib, Tito Naeem [1 ]
机构
[1] Sohag Fac Med, Dept ENT, Sohag, Egypt
关键词
premalignant; malignant; head and neck squamous cell carcinoma; DNA ploidy; DNA image cytometry;
D O I
10.1016/j.oraloncology.2006.04.005
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
We attempted to identify the molecular mechanisms involved in Head and Neck Squamous Cell Carcinoma (HNSCC) pathogenesis by measuring the nuclear DNA content (ploidy) in premalignant (potentially malignant) and malignant patients as compared to normal controts, and to determine whether DNA ploidy could be used to predict the clinical outcome. From March 2001 to December 2003, the analysis was carried out in a set of 41 patients with premalignant lesions and 79 suffering from squamous cell carcinoma of laryngeal, oesophageal, nasopharyngeal, nasal and oral lesions and 50 controls. Representative samples were taken by punch biopsy and processed using standard formol-paraffin technique for histopathological examination. Fifty micrometer thick sections of paraffin-embedded tissues were analyzed to detect the DNA content by image cytometry. Of the potentially malignant patients, 46% had diploid lesions, 37% had tetraptoid lesions and 17% had aneuptoid Lesions. While of the patients with cancer, 90% had aneuptoid lesions, 10% had diploid lesions and none had tetraptoid lesions. DNA diploidy tended to occur earlier in the progression from premalignant to malignant lesions and this helps us early detection of HNSCC by DNA from lesions in high risk groups and examination of its ploidy. Knowledge of tumor cell ploidy by DNA image cytometry may facilitate the evaluation of malignant and premalignant lesions in HNSCC. The present findings are promising to supplement clinical and histopathological parameters in evaluating prognosis and to demonstrate methods that are readily applicable for routine diagnostic work. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:366 / 372
页数:7
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