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一种利用细胞周期蛋白E、Ki-67和ras p21的非小细胞肺癌风险分层模型:G1期细胞周期蛋白在细胞增殖和预后中的不同作用

A risk-stratification model of non-small cell lung cancers using cyclin E, Ki-67, and ras p21: different roles of G1 cyclins in cell proliferation and prognosis.

作者信息

Dosaka-Akita H, Hommura F, Mishina T, Ogura S, Shimizu M, Katoh H, Kawakami Y

机构信息

First Department of Medicine, Hokkaido University School of Medicine, Sapporo, Japan.

出版信息

Cancer Res. 2001 Mar 15;61(6):2500-4.

Abstract

A large number of biological factors that seem to have important prognostic significance have been identified in non-small cell lung cancers (NSCLCs). In the present study, we have characterized expression of cyclin D1 and cyclin E in a cohort of 217 resected NSCLCs from a single institution by immunohistochemistry to analyze their expression in relation to the growth fraction determined by Ki-67 and to prognosis, and then we have constructed a risk-stratification model of cancer death by multiple biological factors in p-stage I NSCLCs. The cyclin E labeling index (LI) was significantly associated with the Ki-67 LI (r = 0.45; P < 0.001). Tumors having high-level cyclin E expression (cyclin E LI > or =30%) showed a significantly higher Ki-67 LI than tumors having low-level cyclin E expression (cyclin E LI <30%; P < 0.001), whereas positive or negative cyclin D1 expression was not associated with the Ki-67 LI (P = 0.1). Cyclin E expression was a significant and independent unfavorable prognostic factor (hazards ratio = 2.09; P = 0.03), as reported previously (Clin. Cancer Res., 6: 11-16, 2000), whereas cyclin D1 expression was not. These findings indicate different roles of cyclin D1 and cyclin E in cell proliferation and in the prognosis of NSCLCs. Furthermore, we stratified this cohort of p-stage I NSCLCs into different survival groups by using biological factors, including cyclin E, Ki-67, and ras p21, which previously we have found to be independent prognostic factors among 10 factors studied in p-stage I NSCLCs. Four groups of patients with markedly different survivals were identified with 5-year survival rates that ranged from 96% for patients with no factors altered to 41% for patients with all three factors altered (P < 0.001). This combination of biological factors was a significant and independent prognostic factor (hazards ratio = 7.94; P = 0.001).

摘要

在非小细胞肺癌(NSCLC)中,已确定大量似乎具有重要预后意义的生物学因素。在本研究中,我们通过免疫组织化学对来自单一机构的217例切除的NSCLC队列中的细胞周期蛋白D1和细胞周期蛋白E的表达进行了表征,以分析它们与由Ki-67确定的生长分数以及预后的关系,然后我们构建了I期p阶段NSCLC中由多种生物学因素导致癌症死亡的风险分层模型。细胞周期蛋白E标记指数(LI)与Ki-67 LI显著相关(r = 0.45;P < 0.001)。细胞周期蛋白E高表达(细胞周期蛋白E LI>或= 30%)的肿瘤显示出比细胞周期蛋白E低表达(细胞周期蛋白E LI < 30%;P < 0.001)的肿瘤显著更高的Ki-67 LI,而细胞周期蛋白D1的阳性或阴性表达与Ki-67 LI无关(P = 0.1)。如先前报道(Clin. Cancer Res., 6: 11 - 16, 2000),细胞周期蛋白E表达是一个显著且独立的不良预后因素(风险比 = 2.09;P = 0.03),而细胞周期蛋白D1表达则不是。这些发现表明细胞周期蛋白D1和细胞周期蛋白E在NSCLC的细胞增殖和预后中具有不同作用。此外,我们使用生物学因素,包括细胞周期蛋白E、Ki-67和ras p21,将这个I期p阶段NSCLC队列分层为不同的生存组,我们之前在I期p阶段NSCLC研究的10个因素中发现这些因素是独立的预后因素。确定了四组生存率明显不同的患者,5年生存率从无因素改变的患者的96%到所有三个因素都改变的患者的41%不等(P < 0.001)。这种生物学因素的组合是一个显著且独立的预后因素(风险比 = 7.94;P = 0.001)。

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