Expression of cyclins A and D and p21(waf1/cip1) proteins in renal cell cancer and their relation to clinicopathological variables and patient survival.

Expression of cyclins A and D and p21(waf1/cip1) proteins in renal cell cancer and their relation to clinicopathological variables and patient survival.
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DOI:
10.1038/sj.bjc.6690634
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发表时间:
1999-08
影响因子:
8.8
通讯作者:
Kosma, VM
Kosma, VM
中科院分区:
医学1区
文献类型:
--
作者:
Aaltomaa, S;Lipponen, P;Ala-Opas, M;Eskelinen, M;Syrjänen, K;Kosma, VM

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我们研究了118例肾细胞癌,分析细胞周期蛋白A和D1和p21(waf 1/cip 1)的表达,以及它们与临床和组织病理学参数以及临床预后的关系。正常肾组织中不表达细胞周期蛋白A、D1和细胞周期蛋白依赖性激酶抑制剂p21(waf 1/cip 1)。cyclin D1和p21(waf 1/cip 1)的染色信号总是在细胞核中,但cyclin A也在肿瘤细胞的胞浆中表达。细胞周期蛋白A、细胞周期蛋白D1和p21(waf 1/cip 1)阳性肿瘤细胞的平均(范围)分数分别为2.2%(范围0-20%)、23.3%(范围0-90%)和6.8%(范围0-70%)。cyclin A的表达与肿瘤的静脉浸润、高核分级、高核分裂率、高Ki-67和高PCNA表达有关(P均≤ 0.006)。cyclin D1的表达与年龄> 65岁、核分级低、p53高表达有关(均P ≤ 0.05)。p21(waf 1/cip 1)与cyclin D1呈负相关(P = 0.011)。细胞周期蛋白A预测了整个研究组(P = 0.0014)、T1-4/N 0 -2/M0(P = 0.0007)和T1-2/N 0/M0肿瘤(P = 0.0007)的生存率。细胞周期蛋白A也是T1-4/N 0/M0(P = 0.0027)肿瘤(P = 0.0007)无病生存期的有力预测因子。细胞周期蛋白D1和p21(waf 1/cip 1)与任何组的生存率或无病生存率均无显著相关。在所有病例中,影响预后的独立因素有远处转移(相对危险度(RR)5.16,P < 0.001)、T细胞分类(RR 2.68,P < 0.001)、Ki-67表达(RR 1.02,P = 0.026)和cyclin A表达(RR 1.12,P = 0.001)。T1-4/N 0/M0期肿瘤的独立预测因子为T分类(RR 2.67,P = 0.001)和细胞周期蛋白A(RR 1.21,P < 0.001),T1-2/N 0/M0期肿瘤的唯一显著预测因子为细胞周期蛋白A(RR 1.19,P = 0.0002)。在肾细胞癌中,细胞周期蛋白A是一个强大的和独立的预后因素,在疾病的所有临床阶段,而细胞周期蛋白D1和p21(waf 1/cip 1)没有预后价值。© 1999癌症研究运动
We have studied 118 renal cell carcinomas to analyse the expressions of cyclins A and D1 and p21(waf1/cip1), and their relationship to clinical and histopathological parameters as well as to clinical outcome. Cyclins A and D1 and cyclin-dependent kinase inhibitor p21(waf1/cip1) were not expressed in normal renal tissue. Staining signals of cyclin D1 and p21(waf1/cip1) were always nuclear but cyclin A was also expressed in the cytoplasm of the tumour cells. The mean (range) fractions of cyclin A, cyclin D1 and p21(waf1/cip1)-positive tumour cells were 2.2% (range 0–20%), 23.3% (range 0–90%) and 6.8% (range 0–70%) respectively. The expression of cyclin A was related to venous invasion, high nuclear grade, high mitotic rate, high Ki-67 and high PCNA expressions (P ≤ 0.006 for all). The expression of cyclin D1 was linked with age over 65 years, low nuclear grade and high p53 expression (P ≤ 0.05 for all). An inverse correlation was present between p21(waf1/cip1) and cyclin D1 (P = 0.011). Cyclin A predicted survival in the entire study group (P = 0.0014), in T1–4/N0–2/M0 (P = 0.0007) and in T1–2/N0/M0 tumours (P = 0.0007). Cyclin A was also a powerful predictor of disease-free survival in T1–4/N0/M0 (P = 0.0027) tumours (P = 0.0007). Cyclin D1 and p21(waf1/cip1) were not significantly related to survival or disease-free survival in any of the groups. In the entire material the independent prognostic factors were the presence of distant metastases (relative risk (RR) 5.16, P < 0.001), T category (RR 2.68, P < 0.001), Ki-67 expression (RR 1.02, P = 0.026) and cyclin A expression (RR 1.12, P = 0.001). The independent predictors in T1–4/N0/M0 tumours were T-category (RR 2.67, P = 0.001) and cyclin A (RR 1.21, P < 0.001), and in T1–2/N0/M0 tumours the only significant predictor was cyclin A (RR 1.19, P = 0.0002). In renal cell carcinoma, cyclin A is a powerful and independent prognostic factor in all clinical stages of the disease, whereas cyclin D1 and p21(waf1/cip1) have no prognostic value. © 1999 Cancer Research Campaign
DOI: 10.1046/j.1464-410x.1997.03399.x
发表时间: 1997-02-01
期刊: BRITISH JOURNAL OF UROLOGY
影响因子: --
作者:
Byrne, RL;Horne, CHW;Hamdy, FC
通讯作者: Hamdy, FC
DOI: 10.1159/000019721
发表时间: 1998-09-01
期刊: EUROPEAN UROLOGY
影响因子: 23.4
作者:
Lipponen, P;Aaltomaa, S;Kosma, VM
通讯作者: Kosma, VM
DOI: 10.1002/ijc.2910570224
发表时间: 1994-04-15
影响因子: 6.4
作者:
LIPPONEN, P;ESKELINEN, M;SYRJANEN, K
通讯作者: SYRJANEN, K
DOI: 10.1016/s0090-4295(96)00493-1
发表时间: 1997-03-01
期刊: UROLOGY
影响因子: 2.1
作者:
Papandreou, CN;Bogenrieder, T;Nanus, DM
通讯作者: Nanus, DM
DOI: 10.1016/s0344-0338(89)80191-8
发表时间: 1989-11-01
影响因子: 2.8
作者:
HAAPASALO, H;PESONEN, E;COLLAN, Y
通讯作者: COLLAN, Y