Ghazizadeh Mohammad, Jin Enjing, Shimizu Hajime, Fujiwara Masakazu, Arai Satoru, Ohaki Yoshiharu, Takemura Tamiko, Kawanami Oichi
Department of Molecular Pathology, Institute of Gerontology, Nippon Medical School, Nakahara-ku, Kawasaki, Japan.
Respiration. 2005 Jan-Feb;72(1):68-73. doi: 10.1159/000083403.
The p16(INK4) protein has been identified as a potent inhibitor of cyclin-dependent kinase (cdk)4 by blocking cdk4-mediated phosphorylation of the tumor suppressor retinoblastoma (Rb) protein, thus allowing Rb-mediated growth suppression.
Loss of p16(INK4) has been associated with a poor cancer prognosis, but its potential significance in bronchioloalveolar carcinomas (BACs) has not been explored.
We examined immunohistochemical expression of p16(INK4), cdk4, and Rb proteins in 38 BACs and correlated their expression levels with known clinicopathological features of the disease.
All BACs expressed cdk4, while 89 and 82% expressed p16(INK4) and Rb proteins, respectively. None of the clinicopathological factors correlated with p16(INK4), cdk4, or Rb expression separately. A low p16(INK4)/cdk4 ratio was significantly associated with a high disease stage (p = 0.04), and the ratio tended to be lower in mucinous than nonmucinous tumors. BACs with a low p16(INK4)/cdk4 ratio showed significantly higher Rb expression levels (p = 0.02). Univariable survival analyses showed a significantly lower 5-year survival probability in patients with a high stage (p = 0.002) or low p16(INK4)/cdk4 ratio (p = 0.01).
The results suggest a role of the cdk4/p16(INK4) pathway in the prognosis of BACs. Further studies are warranted to clarify whether a low p16(INK4)/cdk4 ratio may identify tumors that are destined to behave unfavorably.
p16(INK4)蛋白已被确定为细胞周期蛋白依赖性激酶(cdk)4的有效抑制剂,它通过阻断cdk4介导的肿瘤抑制蛋白视网膜母细胞瘤(Rb)的磷酸化,从而实现Rb介导的生长抑制。
p16(INK4)缺失与癌症预后不良相关,但其在细支气管肺泡癌(BAC)中的潜在意义尚未得到探索。
我们检测了38例BAC中p16(INK4)、cdk4和Rb蛋白的免疫组化表达,并将它们的表达水平与该疾病已知的临床病理特征进行关联分析。
所有BAC均表达cdk4,而分别有89%和82%表达p16(INK4)和Rb蛋白。没有任何临床病理因素分别与p16(INK4)、cdk4或Rb表达相关。低p16(INK4)/cdk4比值与高疾病分期显著相关(p = 0.04),且黏液性肿瘤中的该比值往往低于非黏液性肿瘤。p16(INK4)/cdk4比值低的BAC显示出显著更高的Rb表达水平(p = 0.02)。单因素生存分析显示,高分期(p = 0.002)或低p16(INK4)/cdk4比值(p = 0.01)的患者5年生存概率显著更低。
结果提示cdk4/p16(INK4)通路在BAC预后中发挥作用。有必要进一步研究以明确低p16(INK4)/cdk4比值是否可识别预后不良的肿瘤。