Lemaire F, Millon R, Young J, Cromer A, Wasylyk C, Schultz I, Muller D, Marchal P, Zhao C, Melle D, Bracco L, Abecassis J, Wasylyk B
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, 1 Rue Laurent Fries, BP 10142, 67404 Illkirch cedex, France.
Br J Cancer. 2003 Nov 17;89(10):1940-9. doi: 10.1038/sj.bjc.6601373.
Head and neck squamous cell carcinoma (HNSCC) is the fifth most common cancer in men with an incidence of about 780000 new cases per year worldwide and a poor rate of survival. There is a need for a better understanding of HNSCC, for the development of rational targeted interventions and to define new prognostic or diagnostic markers. To address these needs, we performed a large-scale differential display comparison of hypopharyngeal HNSCCs against histologically normal tissue from the same patients. We have identified 70 genes that exhibit a striking difference in expression between tumours and normal tissues. There is only a limited overlap with other HNSCC gene expression studies that have used other techniques and more heterogeneous tumour samples. Our results provide new insights into the understanding of HNSCC. At the genome level, a series of differentially expressed genes cluster at 12p12-13 and 1q21, two hotspots of genome disruption. The known genes share functional relationships in keratinocyte differentiation, angiogenesis, immunology, detoxification, and cell surface receptors. Of particular interest are the 13 'unknown' genes that exist only in EST, theoretical cDNA and protein databases, or as chromosomal locations. The differentially expressed genes that we have identified are potential new markers and therapeutic targets.
头颈部鳞状细胞癌(HNSCC)是男性中第五大常见癌症,全球每年新发病例约780000例,生存率较低。有必要更好地了解HNSCC,开发合理的靶向干预措施并确定新的预后或诊断标志物。为满足这些需求,我们对下咽HNSCC与同一患者的组织学正常组织进行了大规模差异显示比较。我们鉴定出70个在肿瘤组织和正常组织之间表达存在显著差异的基因。与使用其他技术和更异质性肿瘤样本的其他HNSCC基因表达研究仅有有限的重叠。我们的结果为理解HNSCC提供了新的见解。在基因组水平上,一系列差异表达基因聚集在12p12 - 13和1q21,这是基因组破坏的两个热点区域。已知基因在角质形成细胞分化、血管生成、免疫学、解毒和细胞表面受体方面具有功能关系。特别令人感兴趣的是13个“未知”基因,它们仅存在于EST、理论cDNA和蛋白质数据库中,或作为染色体位置存在。我们鉴定出的差异表达基因是潜在的新标志物和治疗靶点。