Liao Wen-Ting, Wang Xi, Xu Li-Hua, Kong Qing-Li, Yu Chun-Ping, Li Man-Zhi, Shi Ling, Zeng Mu-Sheng, Song Li-Bing
State Key Laboratory of Oncology in Southern China, Guangzhou, Guangdong, China.
Cancer. 2009 Apr 1;115(7):1507-17. doi: 10.1002/cncr.24128.
Lung cancer is 1 of the leading causes of cancer death worldwide, and the high mortality from this disease is caused mainly by the lack of efficient diagnostic strategies for early-stage lung cancer. The objective of the current study was to investigate the expression pattern and clinicopathologic significance of centromere protein H (CENP-H) in patients with nonsmall cell lung cancer (NSCLC).
The expression profile of CENP-H in normal lung epithelial cells, NSCLC cell lines, NSCLC tissues, and adjacent noncancerous lung tissues were detected by reverse transcription-polymerase chain reaction (RT-PCR), real-time RT-PCR, and Western blot analysis. The expression level of CENP-H in 223 NSCLC tissues was measured by immunohistochemistry staining. Statistical analysis was performed to evaluate the clinicopathologic significance of CENP-H.
The expression level of CENP-H was much higher in cancer cell lines and lung cancer tissues than that in normal cells and adjacent noncancerous lung tissues, respectively. Immunohistochemical analysis revealed positive CENP-H expression in 118 of 223 NSCLC tissues (52.9%). Statistical analysis revealed that CENP-H expression was correlated strongly with clinical stage (P=.018), tumor classification (P=.03), and Ki-67 expression (P < .001). Patients with lower CENP-H expression had better overall survival than patients with higher CENP-H expression. Further analysis suggested that CENP-H could predict prognosis only in patients with early-stage disease. Multivariate analysis suggested that CENP-H expression was an independent prognostic marker for survival in patients with NSCLC.
The current results demonstrated that high CENP-H protein expression was related to poor outcome in patients with NSCLC. CENP-H may be used as a prognostic biomarker for patients lung patients, especially those with early-stage NSCLC.
肺癌是全球癌症死亡的主要原因之一,该疾病的高死亡率主要是由于缺乏针对早期肺癌的有效诊断策略。本研究的目的是调查着丝粒蛋白H(CENP-H)在非小细胞肺癌(NSCLC)患者中的表达模式及临床病理意义。
通过逆转录聚合酶链反应(RT-PCR)、实时RT-PCR和蛋白质免疫印迹分析,检测正常肺上皮细胞、NSCLC细胞系、NSCLC组织及相邻非癌肺组织中CENP-H的表达谱。采用免疫组织化学染色法检测223例NSCLC组织中CENP-H的表达水平。进行统计学分析以评估CENP-H的临床病理意义。
CENP-H在癌细胞系和肺癌组织中的表达水平分别明显高于正常细胞和相邻非癌肺组织。免疫组织化学分析显示,223例NSCLC组织中有118例(52.9%)CENP-H表达呈阳性。统计学分析显示,CENP-H表达与临床分期(P=0.018)、肿瘤分类(P=0.03)和Ki-67表达(P<0.001)密切相关。CENP-H表达较低的患者总生存期优于CENP-H表达较高的患者。进一步分析表明,CENP-H仅能预测早期疾病患者的预后。多因素分析表明,CENP-H表达是NSCLC患者生存的独立预后标志物。
目前的结果表明,NSCLC患者中CENP-H蛋白高表达与不良预后相关。CENP-H可用作肺癌患者尤其是早期NSCLC患者的预后生物标志物。