Jing Yue, Zhou Qian, Zhu Huidong, Zhang Ye, Song Yuxian, Zhang Xiaoxin, Huang Xiaofeng, Yang Yan, Ni Yanhong, Hu Qingang
Central Laboratory, Nanjing Stomatological Hospital, Medical School of Nanjing University, Nanjing, Jiangsu 210008, P.R. China.
Department of Oral and Maxillofacial Surgery, Nanjing Stomatological Hospital, Medical School of Nanjing University, Nanjing, Jiangsu 210008, P.R. China.
Oncol Lett. 2019 Jan;17(1):974-980. doi: 10.3892/ol.2018.9647. Epub 2018 Oct 31.
As a nuclear and nucleolar protein, proliferation marker protein Ki-67 (Ki-67) serves a vital role in tumorigenesis due to its positive correlation with tumor proliferation. High expression of Ki-67 in the cell cycle from the G to M phase makes it a potential biomarker for certain tumors and useful for selecting medical treatment. However, the diagnostic value of Ki-67 in oral squamous cell carcinoma (OSCC) has not been fully evaluated. In the present study, the objective was the elucidation of the prognostic value of Ki-67 in a large number of OSCC patients. Ki-67 expression was detected by immunohistochemical staining methods in 298 OSCC specimens and 98 tumor-free oral mucosa specimens (62 dysplasia mucosa and 36 normal mucosa), acquired from Nanjing Stomatological Hospital, Medical School of Nanjing University (Nanjing, China). Expression of Ki-67 in normal tissues, dysplasia tissues and OSCC tissues was compared. Associations between Ki-67 expression and clinicopathological parameters were analyzed by χ test. Kaplan-Meier survival curves and Cox progression analysis were used to assess the diagnostic value of Ki-67 for OSCC. The results showed that Ki-67 expression was higher in OSCC tissues than in tumor-free tissues and that it increased with the progression of dysplasia in oral mucosa tissues. In addition, patients with high Ki-67 expression had a worse clinical outcome, including poor tumor differentiation (P=0.001), increased positive lymph node metastasis (P=0.006) and increased worst pattern of invasion type (P<0.0001). Kaplan-Meier survival analysis demonstrated that higher Ki-67 expression was associated with poorer overall survival (OS) (P=0.035), recurrence-free survival (RFS) (P=0.017), metastasis-free survival (MFS) (P=0.032) and disease-free survival (DFS) (P=0.018) times. Additional multivariate analysis demonstrated that Ki-67 expression was negatively associated with OS, DFS, RFS and MFS. In conclusion, Ki-67 overexpression is associated with the progression of OSCC and serves as an independent prognostic factor for OSCC patients.
作为一种核蛋白和核仁蛋白,增殖标志物蛋白Ki-67由于其与肿瘤增殖呈正相关,在肿瘤发生中起着至关重要的作用。Ki-67在从G期到M期的细胞周期中高表达,使其成为某些肿瘤的潜在生物标志物,并有助于选择治疗方案。然而,Ki-67在口腔鳞状细胞癌(OSCC)中的诊断价值尚未得到充分评估。在本研究中,目的是阐明Ki-67在大量OSCC患者中的预后价值。采用免疫组织化学染色方法检测了从南京大学医学院附属南京口腔医院(中国南京)获取的298例OSCC标本和98例无瘤口腔黏膜标本(62例发育异常黏膜和36例正常黏膜)中Ki-67的表达。比较了Ki-67在正常组织、发育异常组织和OSCC组织中的表达。采用χ检验分析Ki-67表达与临床病理参数之间的相关性。采用Kaplan-Meier生存曲线和Cox进展分析评估Ki-67对OSCC的诊断价值。结果显示,Ki-67在OSCC组织中的表达高于无瘤组织,且在口腔黏膜组织中随发育异常的进展而增加。此外,Ki-67高表达的患者临床结局较差,包括肿瘤分化差(P=0.001)、阳性淋巴结转移增加(P=0.006)和侵袭类型最差模式增加(P<0.0001)。Kaplan-Meier生存分析表明,较高的Ki-67表达与较差的总生存期(OS)(P=0.035)、无复发生存期(RFS)(P=0.017)、无转移生存期(MFS)(P=0.032)和无病生存期(DFS)(P=0.018)相关。进一步的多因素分析表明,Ki-67表达与OS、DFS、RFS和MFS呈负相关。总之Ki-67过表达与OSCC的进展相关,是OSCC患者的独立预后因素。