Wang J, Bi Y H, Yang J, Liu F, Li Y K, Cui H Y, Wang F, Liu J, Yang B, Zhang L
Translational Medicine Research Center, Shanxi Medical University, Taiyuan 030001, China.
Department of Material Evidence, College of Forensic Medicine, Shanxi Medical University, Taiyuan 030001, China.
Zhonghua Zhong Liu Za Zhi. 2017 Jan 23;39(1):7-12. doi: 10.3760/cma.j.issn.0253-3766.2017.01.002.
To investigate the function and mechanism of zinc finger protein 750 (ZNF750) in esophageal squamous cell carcinoma (ESCC). Xenograft in nude mice was applied to detect the tumorigenesis of ZNF750-depleted ESCC cells. Western blot was performed to observe the expression of downstream target protein of ZNF750 in ESCC cell lines and xenograft tumor tissues in which ZNF750 was knocked down. 3-(4, 5-dimethyl-2-thiazolyl)-2, 5-diphenyl-2H tetrazolium bromide (MTT) assay was used to determine the proliferation of ZNF750 stably depleted cells after restoration of its target protein. The tumor weight of blank control, negative control and ZNF750 knockdown groups was 137±26 mg, 161±31 mg and 463±89 mg, respectively, with a statistically significant difference (<0.01). The expressions of Kruppel-like factor 4 (KLF4) in ZNF750-depleted ESCC cells and its derived tumor tissue xenograft in nude mice were significantly down-regulated. Restoration of KLF4 in ZNF750 stably depleted cells significantly inhibited the cell proliferation (<0.01). ZNF750 may be a new tumor suppressor in the tumorigenesis of ESCC, and the inhibition of cell proliferation induced by ZNF750 may be partially through the regulation of KLF4 expression.
研究锌指蛋白750(ZNF750)在食管鳞状细胞癌(ESCC)中的作用及机制。应用裸鼠异种移植模型检测ZNF750缺失的ESCC细胞的肿瘤发生情况。采用蛋白质免疫印迹法观察ZNF750敲低的ESCC细胞系和异种移植瘤组织中ZNF750下游靶蛋白的表达。使用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2H四唑溴盐(MTT)法测定其靶蛋白恢复后ZNF750稳定缺失细胞的增殖情况。空白对照组、阴性对照组和ZNF750敲低组的肿瘤重量分别为137±26mg、161±31mg和463±89mg,差异有统计学意义(<0.01)。ZNF750缺失的ESCC细胞及其裸鼠异种移植瘤组织中 Kruppel样因子4(KLF4)的表达明显下调。在ZNF750稳定缺失的细胞中恢复KLF4表达可显著抑制细胞增殖(<0.01)。ZNF750可能是ESCC肿瘤发生过程中的一种新的肿瘤抑制因子,ZNF750诱导的细胞增殖抑制可能部分通过调节KLF4表达实现。