Harada Koji, Ferdous Tarannum, Minami Haruyasu, Mishima Katsuaki
Department of Oral and Maxillofacial Surgery, Yamaguchi University Graduate School of Medicine, Ube, Yamaguchi 755-8505, Japan.
Mol Clin Oncol. 2019 Jan;10(1):29-36. doi: 10.3892/mco.2018.1770. Epub 2018 Nov 19.
Forkhead box protein M1 (FOXM1) is an oncoprotein that is involved in cell proliferation, differentiation and aging, and overexpression of FOXM1 is thought to be associated with the development and progression of various types of cancer. The expression of FOXM1 was retrospectively examined in tumor tissues taken from 56 oral squamous cell carcinoma (OSCC) patients by immunohistochemical staining. All of these patients received docetaxel (Doc)-containing regimens as treatments against OSCC. The association between FOXM1 expression and the clinicopathological characteristics and prognosis of these patients was then examined. FOXM1 was expressed in the nucleus and cytoplasm of OSCC tissues samples. There was a significant association between FOXM1 expression in tumor tissues and N classification (P=0.0395), stage (P=0.004), therapeutic efficacy (P=0.0113) and outcome (P=0.0134) of patients. However, FOXM1 expression had no association with patients' sex, age or T classification. Additionally, high expression of FOXM1 in tumor cells was associated with a shorter overall survival (P=0.0257) of patients. Multivariate analysis also revealed that elevated expression of FOXM1 was a predictor of patients' poor survival (P=0.0327). The results suggested that high expression of FOXM1 in OSCC tumors may result in reduced therapeutic effects and poor clinical outcomes of patients receiving Doc-based treatment regimens.
叉头框蛋白M1(FOXM1)是一种癌蛋白,参与细胞增殖、分化和衰老,FOXM1的过表达被认为与各种癌症的发生和发展有关。通过免疫组织化学染色对56例口腔鳞状细胞癌(OSCC)患者的肿瘤组织中FOXM1的表达进行回顾性检测。所有这些患者均接受含多西他赛(Doc)的方案治疗OSCC。然后检测FOXM1表达与这些患者的临床病理特征及预后之间的关联。FOXM1在OSCC组织样本的细胞核和细胞质中表达。肿瘤组织中FOXM1表达与患者的N分期(P = 0.0395)、分期(P = 0.004)、治疗疗效(P = 0.0113)及预后(P = 0.0134)之间存在显著关联。然而,FOXM1表达与患者的性别、年龄或T分期无关。此外,肿瘤细胞中FOXM1的高表达与患者较短的总生存期(P = 0.0257)相关。多因素分析还显示,FOXM1表达升高是患者生存不良的一个预测指标(P = 0.0327)。结果表明,OSCC肿瘤中FOXM1的高表达可能导致接受基于Doc治疗方案的患者治疗效果降低和临床预后不良。