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Phenotypic alterations in Rb pathway have more prognostic influence than p53 pathway proteins in oral carcinoma

机译:RB途径中的表型改变比口腔癌中的P53途径蛋白质具有更高的预后影响

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The two well-defined pathways that are shown to be prominently altered in a variety of cancers are the cell cycle regulatory pathways led by either p53 or Rb genes. The present study is undertaken to find the pathway that is more altered in oral carcinoma at protein level, with special emphasis on its prognostic significance. The expression pattern of key molecules of the Rb and p53 pathways, such as Rb, cyclin D1, CDK4, p16, p53, p21 and Bcl-2 and the proliferative marker PCNA were analysed in 348 oral carcinoma specimens by immunohistochemical technique. The expression index of these molecules and various clinicopathological factors were statistically correlated with treatment end points to assess its prognostic efficacy after following up these patients up to a maximum of 48 months with a median of 23 months. Rb pathway proteins, Rb (P=0.016), cyclin D1 (P=0.0001) and p16 (P=0.012) showed significant association with disease-free survival, and p16 (P=0.041) and cyclin D1 (P=<0.0001) with the overall survival. Among p53 pathway proteins studied, only p53 expression index showed association with both disease-free survival and overall survival. Multivariate analyses confirmed that the biological variables, cyclin D1 and p16 and the clinical variable, 'stage of disease' were independent predictors of disease-free survival and overall survival. Subgrouping of the patients on the basis of p16 and cyclin D1 expression revealed that the subgroup having downregulation of p16 and overexpression of cyclin D1 exhibited the worst disease-free survival and overall survival compared to the other subgroups. The present data showed that disabling of the Rb and p53 pathways were frequent events in oral carcinoma. The study also demonstrated that the Rb pathway proteins are comparatively more important than p53 pathway proteins for the prognostication of oral carcinoma patients. The combined evaluation of p16 and cyclin D1 in oral carcinoma could identify a group of patients with the worst survival who might therefore need alternate or more intense treatment strategies.
机译:显示出在各种癌症中突出改变的两个明确的途径是通过P53或RB基因引导的细胞周期调节途径。对本研究进行了蛋白质水平在口腔癌中更改变的途径,特别强调其预后意义。通过免疫组化技术分析了RB和P53途径的关键分子的表达模式,例如Rb,Cyclin D1,CDK4,P16,P53,P21和Bcl-2和增殖标记PCNA。这些分子的表达指数和各种临床病理因子与治疗终点有统计学相关,以评估其在后续这些患者最多48个月后的预后疗效,中位数为23个月。 RB途径蛋白,Rb(p = 0.016),细胞周期蛋白D1(p = 0.0001)和p16(p = 0.012)显示出与无疾病存活率的显着关联,P16(p = 0.041)和细胞周期蛋白d1(p = <0.0001)整体生存。在研究P53途径中,只有P53表达指数显示出无病生存和整体存活的关联。多变量分析证实,生物变量,细胞周期蛋白D1和p16和临​​床变量,“疾病阶段”是无病生存和整体存活的独立预测因子。基于p16和细胞周期蛋白D1表达的患者的亚组揭示了具有P16的下调和细胞周期蛋白D1的亚群表现出与其他亚组相比最严重的无病生存和整体存活。本数据显示,禁用RB和P53途径在口腔癌中常见。该研究还证明,RB途径蛋白比P53途径蛋白相对重要,用于口服癌患者的预后。 P16和细胞周期蛋白D1在口腔癌中的组合评估可以鉴定一组患者,因此可能需要替代或更强烈的治疗策略。

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