Pruneri Giancarlo, Pignataro Lorenzo, Valentini Stefano, Fabris Sonia, Maisonneuve Patrick, Carboni Nadia, Pece Salvatore, Capra Maria, Del Curto Barbara, Neri Antonino, Viale Giuseppe
Division of Pathology and Laboratory Medicine, European Institute of Oncology and University of Milan School of Medicine, Milan, Italy.
Clin Cancer Res. 2005 Jan 1;11(1):242-8.
To analyze the prevalence and clinical relevance of cyclin D3 abnormalities in laryngeal squamous cell carcinoma (LSCC).
Cyclin D3 immunoreactivity was evaluated in 223 formalin-fixed and paraffin-embedded samples of LSCC patients with a mean follow-up of 62.8 +/- 43.2 months. The occurrence of cyclin D3 extra signals was analyzed by fluorescence in situ hybridization in 47 randomly selected cases collected in a tissue microarray. Cyclin D1 immunoreactivity had been previously investigated in 133 cases.
Cyclin D3 immunoreactivity and gene extra signals were found in 39.5% and 42.6% of the cases, respectively, and the concordance between immunohistochemical and fluorescence in situ hybridization results was 70.2% (P = 0.0085). Cyclin D3 immunoreactivity was significantly associated with a high risk of death. Multivariate analysis showed that high tumor grade, exophytic/ulcerating tumor type, low performance status, and cyclin D3 immunoreactivity were the only independent predictors of poor overall survival. In the 133 cases analyzed for both cyclin D1 and cyclin D3, patients with cyclin D1+/cyclin D3+ tumors experienced the worst prognosis, patients with cyclin D1-/cyclin D3- exhibited the most prolonged survival, and with cyclin D1-/cyclin D3+ or cyclin D1+/cyclin D3- tumors an intermediate course was associated.
Our data suggest that cyclin D3 immunoreactivity, possibly due to the occurrence of gene extra copies, may represent an adjunct in LSCC patients' prognostication and contribute to identify D-type cyclins as potential targets of newly developed therapies.
分析细胞周期蛋白D3异常在喉鳞状细胞癌(LSCC)中的发生率及临床相关性。
对223例福尔马林固定石蜡包埋的LSCC患者样本进行细胞周期蛋白D3免疫反应性评估,平均随访时间为62.8±43.2个月。通过荧光原位杂交分析47例随机选取的组织芯片病例中细胞周期蛋白D3额外信号的发生情况。此前已对133例病例进行了细胞周期蛋白D1免疫反应性研究。
分别在39.5%和42.6%的病例中发现细胞周期蛋白D3免疫反应性和基因额外信号,免疫组化和荧光原位杂交结果的一致性为70.2%(P = 0.0085)。细胞周期蛋白D3免疫反应性与高死亡风险显著相关。多因素分析显示,高肿瘤分级、外生性/溃疡性肿瘤类型、低体能状态和细胞周期蛋白D3免疫反应性是总体生存不良的唯一独立预测因素。在同时分析细胞周期蛋白D1和细胞周期蛋白D3的133例病例中,细胞周期蛋白D1+/细胞周期蛋白D3+肿瘤患者预后最差,细胞周期蛋白D1-/细胞周期蛋白D3-患者生存期最长,细胞周期蛋白D1-/细胞周期蛋白D3+或细胞周期蛋白D1+/细胞周期蛋白D3-肿瘤患者病程居中。
我们的数据表明,细胞周期蛋白D3免疫反应性可能由于基因额外拷贝的出现,可能有助于LSCC患者的预后评估,并有助于将D型细胞周期蛋白确定为新开发治疗方法的潜在靶点。