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Aberrant expression of NEK2 and its clinical significance in non-small cell lung cancer

机译:NEK2在非小细胞肺癌中的异常表达及其临床意义

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摘要

The purpose of the present study was to identify a potential biomarker that is more effective than those already available for the prognosis of non-small cell lung cancer (NSCLC) patients. The expression of never in mitosis gene A (NIMA)-related kinase 2 (NEK2), minichromosome maintenance complex component 7 (Mcm7) and Ki67 was evaluated in 270 NSCLC tissues using immunohistochemical and immunofluorescence techniques. Associations between protein expression and clinicopathological characters were assessed, and the impact on overall survival was analyzed. High levels of NEK2, Mcm7 and Ki67 expression were detected in 25.9, 35.2 and 24.4% of the NSCLC tissues. Overexpression of NEK2 was detected more frequently in cases with high T and N stages (P<0.0001 and P=0.011, respectively). Correlations were present between the expression of NEK2, Mcm7 and Ki67. Kaplan-Meier curves indicated that the patients with overexpressed NEK2, Mcm7 and Ki67 had a poorer overall survival time compared to those with low expression for all stages (P<0.0001). In particular, the patients with NEK2 overexpression had a poorer prognosis. Multivariate Cox regression analysis showed that NEK2, Mcm7 and Ki67 are independent prognostic indicators for NSCLC. In conclusion, the data indicate that compared with Mcm7 and Ki67, NEK2 may be a more effective tumor proliferation marker of poor prognosis for NSCLC patients, and that NEK2 may represent a novel potential target for NSCLC therapeutic intervention.
机译:本研究的目的是确定一种潜在的生物标志物,该标志物比非小细胞肺癌(NSCLC)患者的预后更有效。使用免疫组织化学和免疫荧光技术评估了270个NSCLC组织中永不表达的有丝分裂基因A(NIMA)相关激酶2(NEK2),微染色体维持复合物成分7(Mcm7)和Ki67的表达。评估蛋白质表达与临床病理特征之间的关联,并分析其对总体生存的影响。在25.9%,35.2%和24.4%的NSCLC组织中检测到高水平的NEK2,Mcm7和Ki67表达。在高T和N分期的病例中,NEK2的过表达更为频繁(分别为P <0.0001和P = 0.011)。 NEK2,Mcm7和Ki67的表达之间存在相关性。 Kaplan-Meier曲线表明,与所有阶段低表达患者相比,NEK2,Mcm7和Ki67高表达患者的总生存时间较差(P <0.0001)。特别是NEK2过表达的患者预后较差。多因素Cox回归分析显示NEK2,Mcm7和Ki67是NSCLC的独立预后指标。总之,数据表明,与Mcm7和Ki67相比,NEK2可能是NSCLC患者预后不良的更有效的肿瘤增殖标志物,并且NEK2可能代表NSCLC治疗干预的新潜在靶标。

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