Otsuka Ryota, Akutsu Yasunori, Sakata Haruhito, Hanari Naoyuki, Murakami Kentaro, Kano Masayuki, Toyozumi Takeshi, Takahashi Masahiko, Matsumoto Yasunori, Sekino Nobufumi, Yokoyama Masaya, Okada Koichiro, Shiraishi Tadashi, Komatsu Aki, Iida Keiko, Matsubara Hisahiro
Department of Frontier Surgery, Graduate School of Medicine, Chiba University, Chiba, Japan.
Oncology. 2018;94(3):142-148. doi: 10.1159/000484932. Epub 2017 Dec 8.
ZNF750, a transcriptional regulator of epidermal differentiation, has been identified as a tumor suppressor in esophageal squamous cell carcinoma (ESCC). The aim of the present study was to investigate the clinical and prognostic significance of ZNF750 expression and to evaluate the effect of ZNF750 knockdown on cell proliferation, migration, and invasion in ESCC.
A total of 124 patients with ESCC who underwent curative esophagectomy were evaluated in this study. The expression of ZNF750 in surgical specimens was immunohistochemically assessed and used in the analysis of clinicopathological features and overall survival (OS). The molecular role of ZNF750 was investigated by ZNF750 knockdown using small interfering RNA (siRNA) in ESCC cell lines.
Low ZNF750 expression had a significant correlation with positive lymph node metastasis (p = 0.028). Furthermore, there was a significant relationship between low expression of ZNF750 in ESCC and a poor OS, and a multivariate analysis showed that low ZNF750 expression was an independent prognostic factor (p = 0.020). The cell growth, migration, and invasion were significantly increased by downregulation of ZNF750.
The low expression of ZNF750 was significantly associated with a poor prognosis, and ZNF750 expression may, therefore, be a reliable prognostic biomarker in ESCC.
ZNF750是一种表皮分化的转录调节因子,已被确定为食管鳞状细胞癌(ESCC)的肿瘤抑制因子。本研究的目的是探讨ZNF750表达的临床和预后意义,并评估ZNF750基因敲低对ESCC细胞增殖、迁移和侵袭的影响。
本研究共评估了124例行根治性食管切除术的ESCC患者。通过免疫组织化学方法评估手术标本中ZNF750的表达,并用于分析临床病理特征和总生存期(OS)。在ESCC细胞系中使用小干扰RNA(siRNA)敲低ZNF750来研究其分子作用。
ZNF750低表达与阳性淋巴结转移显著相关(p = 0.028)。此外,ESCC中ZNF750低表达与不良OS之间存在显著关系,多因素分析显示ZNF750低表达是独立的预后因素(p = 0.020)。ZNF750下调显著增加了细胞生长、迁移和侵袭。
ZNF750低表达与不良预后显著相关,因此ZNF750表达可能是ESCC中一种可靠的预后生物标志物。