Liu Bin, Xu Ke, Jiang Yufeng, Li Xiaoling
Department of Medical Oncology, Liaoning Cancer Hospital and Institute Shenyang 110042, Liaoning, China.
Department of Thoracic Surgery, Liaoning Cancer Hospital and Institute Shenyang 110042, Liaoning, China.
Int J Clin Exp Pathol. 2014 Oct 15;7(11):7863-71. eCollection 2014.
The objective of the current study was to investigate the expression pattern and clinicopathological significance of Period1 (Per1), Period2 (Per2) and Period3 (Per3) in patients with non-small cell lung cancer (NSCLC). In 130 archived NSCLC tissues, the positive rate of Per1 (86/130, 66.2%), Per2 (77/130, 59.2%) and Per3 (82/130, 63.1%) were reduced in human lung cancer samples compared with adjacent normal lung tissues (Per1, 119/130, 91.5%; Per2, 115/130, 88.5%; Per3, 121/130, 93.1%), as measured by immunohistochemical staining. Loss of Per1 was correlated with poor differentiation (P < 0.001), tumor status (P=0.04), high p-TNM stage (P < 0.001) and lymph node metastasis (P=0.045). The similar tendencies were also found in the correlation of the expression of Per2 and Per3 with clinicopathological factors. In addition, a significant correlation was found between Per1 and Per2 (P < 0.001) in 130 cases of NSCLC. Similarly, a significant correlation was found between Per2 and Per3 (P=0.045). Patients with lower expression of Per1, Per2 and Per3 had a shorter survival time than those with higher expression. These results indicate that loss of Per may promote tumor progression in NSCLC, and may serve as a novel prognostic biomarker of NSCLC.
本研究的目的是调查周期蛋白1(Per1)、周期蛋白2(Per2)和周期蛋白3(Per3)在非小细胞肺癌(NSCLC)患者中的表达模式及临床病理意义。在130份存档的NSCLC组织中,通过免疫组织化学染色检测发现,与癌旁正常肺组织相比(Per1,119/130,91.5%;Per2,115/130,88.5%;Per3,121/130,93.1%),人肺癌样本中Per1(86/130,66.2%)、Per2(77/130,59.2%)和Per3(82/130,63.1%)的阳性率降低。Per1缺失与低分化(P < 0.001)、肿瘤状态(P=0.04)、高p-TNM分期(P < 0.001)及淋巴结转移(P=0.045)相关。Per2和Per3表达与临床病理因素的相关性也呈现类似趋势。此外,在130例NSCLC病例中,Per1与Per2之间存在显著相关性(P < 0.001)。同样,Per2与Per3之间也存在显著相关性(P=0.045)。Per1、Per2和Per3低表达的患者比高表达的患者生存时间更短。这些结果表明,Per缺失可能促进NSCLC的肿瘤进展,并可能作为NSCLC一种新的预后生物标志物。