Piccinin S, Gasparotto D, Vukosavljevic T, Barzan L, Sulfaro S, Maestro R, Boiocchi M
Division of Experimental Oncology 1, Centro di Riferimento Oncologico, Aviano (PN), Italy.
Br J Cancer. 1998 Nov;78(9):1147-51. doi: 10.1038/bjc.1998.644.
Patients affected by squamous cell carcinoma of the head and neck (HNSCC) show frequent occurrence of multiple cancers and widespread precancerous lesions in the mucosa of the upper respiratory tract, a phenomenon known as field cancerization. In this study, we investigated the role of genetic instability in the development of HNSCC and in particular in tumour multiplicity phenomena of the upper respiratory tract. For this purpose, we analysed microsatellite instability (MI) and loss of heterozygosity (LOH) at 20 loci mapping on five chromosomal arms in 67 HNSCC patients, 45 of whom had a single cancer and 22 had multiple primary tumours. The possible involvement of the hMLH1 gene in genetic instability and as a potential target of 3p21 deletion phenomena in head and neck cancers was also investigated. Our data indicate that mismatch repair-related genetic instability plays a minor role in the carcinogenesis of HNSCC and in tumour multiplicity of the head and neck region. Moreover, our results exclude a role for the hMLH1 gene as a determinant of MI and as a specific gene target of deletion at 3p21 in HNSCC. We conclude that presumably other genetic mechanisms, such as those hypothesized for MI-negative hereditary non-polyposis colorectal cancer patients, may play a major role in the carcinogenesis of the mucosa of the upper respiratory tract.
头颈部鳞状细胞癌(HNSCC)患者的上呼吸道黏膜频繁出现多种癌症及广泛的癌前病变,这一现象被称为场癌化。在本研究中,我们调查了基因不稳定在HNSCC发生发展中的作用,特别是在上呼吸道肿瘤多发现象中的作用。为此,我们分析了67例HNSCC患者五条染色体臂上20个位点的微卫星不稳定(MI)和杂合性缺失(LOH),其中45例为单发癌,22例为多发原发性肿瘤。我们还研究了hMLH1基因在基因不稳定中的可能作用以及作为头颈癌3p21缺失现象潜在靶点的情况。我们的数据表明,错配修复相关的基因不稳定在HNSCC的致癌过程及头颈部区域肿瘤多发中起次要作用。此外,我们的结果排除了hMLH1基因作为MI的决定因素以及作为HNSCC中3p21缺失的特定基因靶点的作用。我们得出结论,推测其他遗传机制,如那些为MI阴性的遗传性非息肉病性结直肠癌患者所假设的机制,可能在上呼吸道黏膜的致癌过程中起主要作用。