Section of Oncology, Institute of Medicine, University of Bergen, Bergen 5021, Norway.
Br J Cancer. 2012 Feb 14;106(4):756-62. doi: 10.1038/bjc.2011.548.
Our purpose was to investigate if dysregulation of cell adhesion molecules could be linked to prognosis in squamous cell carcinomas (SCCs) of the anal region.
Protein expression of desmoglein-1 (DSG1), desmocollin-1 (DSC1) and E-cadherin was studied by immunohistochemistry in a cohort of 53 anal carcinoma patients treated by radiation alone or combined with 5-fluorouracil and mitomycin C.
Univariate analyses identified, among others, negative membranous DSG1 staining (P=0.009), negative cytoplasmic DSC1 staining (P=0.012) and negative DSG1 (membranous)+negative DSC1 (cytoplasmic) staining (P=0.004) to be associated with improved cancer-specific survival (CSS). On multivariate analyses positive DSG1 (membranous)+DSC1 (cytoplasmic) staining (HR 6.95, P=0.044), large tumour size and lymph node metastases (HR 6.44, P=0.004) and radiation without chemotherapy (HR 6.73 P=0.004) were associated with worse CSS. On univariate analysis, improved disease-free survival was associated with negative membranous staining of DSG1 (P=0.047), and negative DSG1 (membranous)+negative DSC1 (cytoplasmic) staining (P=0.025), among others.
Membrane negativity for DSG1 and cytoplasmic negativity for DSC1 are favourable markers for CSS in SCCs of the anal region.
我们的目的是研究细胞黏附分子的失调是否与肛门区域鳞状细胞癌(SCC)的预后有关。
采用免疫组织化学方法检测 53 例接受单纯放疗或联合氟尿嘧啶和丝裂霉素 C 治疗的肛门癌患者的桥粒蛋白-1(DSG1)、桥粒蛋白-2(DSC2)和 E-钙黏蛋白的蛋白表达。
单因素分析发现,膜性 DSG1 染色阴性(P=0.009)、细胞质 DSC1 染色阴性(P=0.012)和 DSG1(膜性)+DSC1(细胞质)染色阴性(P=0.004)与癌症特异性生存(CSS)改善相关。多因素分析显示,膜性 DSG1+细胞质 DSC1 染色阳性(HR 6.95,P=0.044)、肿瘤体积大、淋巴结转移(HR 6.44,P=0.004)和单纯放疗无化疗(HR 6.73,P=0.004)与 CSS 较差相关。单因素分析显示,DFS 改善与 DSG1 膜性染色阴性(P=0.047)和 DSG1(膜性)+DSC1(细胞质)染色阴性(P=0.025)有关。
DSG1 膜阴性和 DSC1 细胞质阴性是肛门区域 SCC 患者 CSS 的有利标志物。