Feng Yan, Zhang Haili, Gao Wei, Wen Shuxin, Huangfu Hui, Sun Ruifang, Bai Wei, Wang Binquan
Department of Otolaryngology, Head and Neck Surgery, The First Hospital, Shanxi Medical University, Taiyuan, Shanxi 030001, P.R. China ; Nursing College of Shanxi Medical University, Taiyuan, Shanxi 030001, P.R. China.
Department of Otolaryngology, Head and Neck Surgery, The First Hospital, Shanxi Medical University, Taiyuan, Shanxi 030001, P.R. China.
Oncol Lett. 2014 Oct;8(4):1575-1580. doi: 10.3892/ol.2014.2367. Epub 2014 Jul 22.
DNA topoisomerase II-α (Topo II-α) is essential for numerous cell processes, including DNA replication, transcription, recombination, and chromosome separation and condensation. Altered Topo II-α expression may lead to carcinogenesis and cancer progression. The aim of the present study was to investigate the association between Topo II-α expression levels and clinicopathological data from laryngeal cancer patients. Immunohistochemistry was used to analyze Topo II-α expression in laryngeal squamous cell carcinoma and distant healthy tissues obtained from 70 patients. In addition, fluorescence hybridization was used to detect Topo II-α amplification and chromosome 17 ploidy using a laryngeal cancer tissue microarray. The expression of Topo II-α protein was detected in 71.43% (50/70) of laryngeal carcinoma tissues, in contrast to 9% of healthy tissues (2/22). Furthermore, the expression of Topo II-α protein was found to be associated with tumor de-differentiation and advanced tumor T stage. However, the expression of Topo II-α protein was not identified to be associated with amplification in laryngeal carcinoma, although was found to positively correlate with chromosome 17 aneuploidy (P<0.05). A higher aneuploidy rate contributed to increased expression levels of Topo II-α protein. Aberrant Topo II-α expression and chromosome 17 aneuploidy contributed to the development and progression of laryngeal cancer, indicating that targeting Topo II-α may provide a treatment strategy for patients with laryngeal cancer.
DNA拓扑异构酶II-α(Topo II-α)对众多细胞过程至关重要,包括DNA复制、转录、重组以及染色体分离和浓缩。Topo II-α表达改变可能导致癌变和癌症进展。本研究的目的是调查Topo II-α表达水平与喉癌患者临床病理数据之间的关联。采用免疫组织化学分析70例患者的喉鳞状细胞癌及远处健康组织中Topo II-α的表达。此外,利用荧光杂交技术,通过喉癌组织芯片检测Topo II-α扩增和17号染色体倍性。在71.43%(50/70)的喉癌组织中检测到Topo II-α蛋白表达,而在健康组织中这一比例为9%(2/22)。此外,发现Topo II-α蛋白表达与肿瘤去分化和肿瘤T分期进展相关。然而,虽然发现Topo II-α蛋白表达与喉癌中的扩增无关联,但与17号染色体非整倍体呈正相关(P<0.05)。较高的非整倍体率导致Topo II-α蛋白表达水平升高。Topo II-α表达异常和17号染色体非整倍体促进了喉癌的发生和发展,表明靶向Topo II-α可能为喉癌患者提供一种治疗策略。