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SIRT2 expression exhibits potential to serve as a biomarker for disease surveillance and prognosis in the management of cervical cancer patients

机译:SIRT2表达表现出潜在的宫颈癌患者疾病监测和预后的生物标志物

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This study aimed to compare the sirtuin 2 ( SIRT2 ) expression between tumor tissue and adjacent tissue, and to investigate the association of tumor SIRT2 expression with clinical characteristics and survival profiles in cervical cancer patients. One hundred ninety-one cervical cancer patients were reviewed in this retrospective study. All patients underwent surgical resection and had well-preserved tumor tissue and adjacent tissue, which were obtained for SIRT2 expression detection by immunohistochemistry (IHC). Clinical parameters were obtained. Disease free survival (DFS) and overall survival (OS) were calculated. Both SIRT2 expression by IHC score ( P .001) and the percentage of SIRT2 high expression (defined as IHC score 3) ( P .001) were declined in tumor tissue compared with paired adjacent tissue. In addition, SIRT2 expression in tumor tissue was negatively correlated with tumor size ( P = .047), lymph node metastasis ( P = .009) and FIGO stage ( P = .001). And the DFS ( P = .007) as well as OS ( P = .008) were better in patients with SIRT2 high expression compared with patents with SIRT2 low expression. Univariate Cox's proportional hazards regression model analyses revealed that high SIRT2 expression in tumor tissue was a predictive factor for more prolonged DFS ( P = .009) and OS ( P = .011), while multivariate Cox's proportional hazards regression model analysis disclosed that it lacks independent predictive value for DFS ( P = .084) or OS ( P = .132). SIRT2 expression exhibits potential to serve as a biomarker for disease surveillance and prognosis in the management of cervical cancer patients.
机译:本研究旨在比较肿瘤组织和相邻组织之间的Sirtuin 2(SIRT2)表达,并研究肿瘤SIRT2表达与宫颈癌患者中的临床特征和存活谱之间的关系。在这项回顾性研究中审查了一百九十一宫颈癌患者。所有患者接受手术切除并具有保存完全肿瘤组织和相邻组织,可通过免疫组织化学(IHC)获得SIRT2表达检测。获得了临床参数。无疾病存活(DFS)和整体存活(OS)进行了计算。通过IHC得分(P <.001)的SIRT2表达和SIRT2高表达的百分比(定义为IHC得分> 3)(P <.001)与配对相邻组织相比,肿瘤组织中下降。此外,肿瘤组织中的SIRT2表达与肿瘤大小(p = .047),淋巴结转移(p = .009)和FOGPO阶段(P = .001)呈负相关。与SIRT2低表达的专利相比,DFS(P = .007)以及SIRT2高表达的患者更好(p = .008)。单变量Cox的比例危害回归模型分析显示,肿瘤组织中的高SIRT2表达是更长的DFS(P = .009)和OS(P = .011)的预测因素,而多元硬币的比例危险回归模型分析揭示了它缺乏DFS的独立预测值(P = .084)或OS(P = .132)。 SIRT2表达表现出潜力作为宫颈癌患者管理中的疾病监测和预后的生物标志物。

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