Estilo Cherry L, O-Charoenrat Pornchai, Ngai Ivan, Patel Snehal G, Reddy Pabbathi G, Dao Su, Shaha Ashok R, Kraus Dennis H, Boyle Jay O, Wong Richard J, Pfister David G, Huryn Joseph M, Zlotolow Ian M, Shah Jatin P, Singh Bhuvanesh
Dental Service, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.
Clin Cancer Res. 2003 Jun;9(6):2300-6.
Amplification at chromosome 3q26.3 is a common and crucial event in head and neck squamous cell carcinoma (HNSCC), impacting significantly on tumor progression and clinical outcome. Two novel oncogenes, namely squamous cell carcinoma (SCC)-related oncogene (SCCRO) and PIK3CA (gene encoding phosphatidylinositol-3 kinase catalytic alpha-polypeptide), have been identified as targets of 3q26.3 amplification. This study aimed to delineate the role of SCCRO and PIK3CA in the pathogenesis of oral tongue SCC.
The association between gene copy number for SCCRO and PIK3CA measured by fluorescence in situ hybridization and level of mRNA expression quantitated by real-time reverse transcription-PCR was assessed in a panel of human HNSCC cell lines. In addition, gene expression in 49 consecutive primary SCCs of the oral tongue was determined and correlated with clinicopathological characteristics and outcome.
The mRNA level of SCCRO and PIK3CA was significantly correlated to the gene copy number in nine HNSCC cell lines. In addition, the expression level of SCCRO and PIK3CA was significantly greater in malignant tissues compared with those in histologically normal mucosae (2.17- and 2.46-fold, respectively; P < 0.001). Matched tumor normal control analysis revealed that 24.5 and 69.4% of patients expressed high levels of SCCRO and PIK3CA, respectively. Univariate analyses demonstrated that SCCRO overexpression correlated with nodal metastases (P = 0.05) and advanced stage (P = 0.02), whereas PIK3CA overexpression was associated with vascular invasion (P = 0.04). Only SCCRO overexpression was associated with disease-specific (P = 0.04) and overall survival (P = 0.02). Furthermore, SCCRO overexpression remained an independent predictor for cervical nodal metastasis on multivariate regression analysis (chi(2) likelihood ratio = 4.38; P = 0.04).
Although both SCCRO and PIK3CA may play a role in the pathogenesis of oral tongue SCC through amplification at 3q26, SCCRO appears to be a significant predictor of regional metastasis and may be a marker for tumor aggressiveness and clinical outcome.
3q26.3染色体扩增是头颈部鳞状细胞癌(HNSCC)中常见且关键的事件,对肿瘤进展和临床结局有显著影响。已确定两个新的癌基因,即鳞状细胞癌(SCC)相关癌基因(SCCRO)和PIK3CA(编码磷脂酰肌醇-3激酶催化α多肽的基因)是3q26.3扩增的靶点。本研究旨在阐明SCCRO和PIK3CA在口腔舌鳞状细胞癌发病机制中的作用。
通过荧光原位杂交检测SCCRO和PIK3CA的基因拷贝数,并通过实时逆转录PCR定量mRNA表达水平,评估一组人HNSCC细胞系中两者之间的关联。此外,测定了49例连续的口腔舌原发性鳞状细胞癌的基因表达,并将其与临床病理特征及预后相关联。
在9种HNSCC细胞系中,SCCRO和PIK3CA的mRNA水平与基因拷贝数显著相关。此外,与组织学正常黏膜相比,恶性组织中SCCRO和PIK3CA的表达水平显著更高(分别为2.17倍和2.46倍;P<0.001)。配对肿瘤-正常对照分析显示,分别有24.5%和69.4%的患者SCCRO和PIK3CA表达水平高。单因素分析表明,SCCRO过表达与淋巴结转移(P = 0.05)和晚期(P = 0.02)相关,而PIK3CA过表达与血管侵犯(P = 0.04)相关。只有SCCRO过表达与疾病特异性生存(P = 0.04)和总生存(P = 0.02)相关。此外,在多因素回归分析中,SCCRO过表达仍然是颈部淋巴结转移的独立预测因素(χ2似然比 = 4.38;P = 0.04)。
虽然SCCRO和PIK3CA都可能通过3q26扩增在口腔舌鳞状细胞癌的发病机制中起作用,但SCCRO似乎是区域转移的重要预测因素,可能是肿瘤侵袭性和临床结局的标志物。