Cromer Anne, Carles Annaïck, Millon Régine, Ganguli Gitali, Chalmel Frédéric, Lemaire Frédéric, Young Julia, Dembélé Doulaye, Thibault Christelle, Muller Danièle, Poch Olivier, Abecassis Joseph, Wasylyk Bohdan
Institut de Génétique et de Biologie Moléculaire et Cellulaire, CNRS/INSERM/ULP, 1 Rue Laurent Fries, BP 10142, 67404 Illkirch cedex, France.
Oncogene. 2004 Apr 1;23(14):2484-98. doi: 10.1038/sj.onc.1207345.
Head and neck squamous cell carcinoma (HNSCC) is the sixth most common cancer among men in the developed world. There is a need, for both clinical and scientific reasons, to find markers to identify patients with aggressive disease as early as possible, and to understand the events leading to malignant transformation and susceptibility to metastasis. We report the first large-scale gene expression analysis of a unique HNSCC location, the hypopharynx. Four normal and 34 tumour samples were analysed with 12 600 gene microarrays. Clusters of differentially expressed genes were identified in the chromosomal regions 3q27.3, 17q21.2-q21.31, 7q11.22-q22.1 and 11q13.1-q13.3, which, interestingly, have already been identified by comparative genomic hybridization (CGH) as major regions of gene amplification. We showed that six overexpressed genes (EIF4G1, DVL3, EPHB4, MCM7, BRMS1 and SART1) located in these regions are indeed amplified. We report 119 genes that are highly differentially expressed between 'early' tumours and normal samples. Of these, we validated by quantitative PCR six novel poorly characterized genes. These genes are potential new markers of HNSCC. Comparing patients with relatively nonaggressive and aggressive tumours (without or with clinical evidence of metastasis 3 years after surgery), we identified 164 differentially expressed genes potentially involved in the acquisition of metastatic potential. This study contributes to the understanding of HNSCC, staging patients into prognostic groups and identifying high-risk patients who may benefit from more aggressive treatment.
头颈部鳞状细胞癌(HNSCC)是发达国家男性中第六大常见癌症。出于临床和科学两方面的原因,有必要找到标志物以便尽早识别患有侵袭性疾病的患者,并了解导致恶性转化和转移易感性的相关事件。我们报告了对下咽这一独特的HNSCC部位进行的首次大规模基因表达分析。使用12600个基因微阵列对4个正常样本和34个肿瘤样本进行了分析。在染色体区域3q27.3、17q21.2 - q21.31、7q11.22 - q22.1和11q13.1 - q13.3中鉴定出了差异表达基因簇,有趣的是,这些区域已通过比较基因组杂交(CGH)被确定为基因扩增的主要区域。我们发现位于这些区域的6个过表达基因(EIF4G1、DVL3、EPHB4、MCM7、BRMS1和SART1)确实发生了扩增。我们报告了119个在“早期”肿瘤与正常样本之间高度差异表达的基因。其中,我们通过定量PCR验证了6个新的、特征描述较少的基因。这些基因是HNSCC潜在的新标志物。比较具有相对非侵袭性和侵袭性肿瘤的患者(术后3年无转移或有转移的临床证据),我们鉴定出164个可能与获得转移潜能有关的差异表达基因。这项研究有助于加深对HNSCC的理解,将患者分为不同预后组,并识别可能从更积极治疗中获益的高危患者。