Yamazaki K, Hanami K, Nagao T, Asoh A, Sugano I, Ishida Y
Department of Pathology, Teikyo University, Ichihara Hospital, Ichihara, 299-0111, Japan.
Mol Pathol. 2003 Dec;56(6):336-41. doi: 10.1136/mp.56.6.336.
Several studies have reported that dysregulation of beta catenin or k-ras mutation promotes cyclin D1 expression. This study investigated the relation between cyclin D1 expression and clinicopathological parameters in carcinoma of the ampulla of Vater (CAV), and also assessed the relation between increased cyclin D1 expression and beta catenin/k-ras status in this series.
Thirty CAVs were evaluated for cyclin D1 expression by immunohistochemistry in relation to patient clinicopathological features. Aberrant beta catenin expression and k-ras mutation were also investigated by immunostaining and direct sequencing, and related to cyclin D1 expression.
Increased cyclin D1 expression was seen in 17 of 30 CAVs and was significantly correlated with tumour cell proliferation and disease free survival time (p = 0.018, p = 0.018, respectively). Nuclear accumulation of beta catenin was found in nine of 30 cases, including four cases with missense mutations in exon 3 of CTNNB-1, and was significantly correlated with increased cyclin D1 expression (p = 0.003). k-ras gene mutation was detected in 12 of 30 cases, and was also significantly correlated with increased cyclin D1 expression (p = 0.026). Overall, 14 of 17 CAVs with increased cyclin D1 expression showed nuclear accumulation of beta catenin and/or k-ras mutation.
Increased cyclin D1 expression appears to be associated with tumour proliferation and poorer clinical outcome in CAV. It is also associated with both aberrant beta catenin expression and k-ras mutation. These results are consistent with the in vitro data that cyclin D1 can be transactivated by activated beta catenin-T cell factor/LEF and k-ras pathways.
多项研究报告称,β-连环蛋白失调或k-ras突变会促进细胞周期蛋白D1的表达。本研究调查了壶腹癌(CAV)中细胞周期蛋白D1表达与临床病理参数之间的关系,并评估了该系列中细胞周期蛋白D1表达增加与β-连环蛋白/k-ras状态之间的关系。
通过免疫组织化学评估30例CAV的细胞周期蛋白D1表达,并与患者的临床病理特征相关联。还通过免疫染色和直接测序研究了异常β-连环蛋白表达和k-ras突变,并将其与细胞周期蛋白D1表达相关联。
30例CAV中有17例细胞周期蛋白D1表达增加,且与肿瘤细胞增殖和无病生存时间显著相关(分别为p = 0.018,p = 0.018)。30例中有9例发现β-连环蛋白核内积聚,其中4例CTNNB-1外显子3存在错义突变,且与细胞周期蛋白D1表达增加显著相关(p = 0.003)。30例中有12例检测到k-ras基因突变,也与细胞周期蛋白D1表达增加显著相关(p = 0.026)。总体而言,17例细胞周期蛋白D1表达增加的CAV中有14例显示β-连环蛋白核内积聚和/或k-ras突变。
细胞周期蛋白D1表达增加似乎与CAV中的肿瘤增殖和较差的临床结果相关。它还与异常β-连环蛋白表达和k-ras突变均相关。这些结果与细胞周期蛋白D1可被激活的β-连环蛋白-T细胞因子/淋巴样增强因子和k-ras途径反式激活的体外数据一致。