RNF113A promotes the proliferation, migration and invasion, and is associated with a poor prognosis of esophageal squamous cell carcinoma

被引:17
作者
Wang, Lei [1 ,2 ]
Hou, Zhichao [1 ]
Hasim, Ayshamgul [3 ]
Abuduerheman, Abulajiang [1 ]
Zhang, Haiping [1 ]
Niyaz, Madiniyat [4 ]
Awut, Idiris [1 ]
Upur, Halmurat [5 ]
Sheyhidin, Ilyar [1 ]
机构
[1] Xinjiang Med Univ, Dept Thorac Surg, Affiliated Hosp 1, 137 Liyushan Rd, Urumqi 830054, Xinjiang Uygur, Peoples R China
[2] Xinjiang Med Univ, Dept Gastroenterol, Affiliated Hosp 1, 137 Liyushan Rd, Urumqi 830054, Xinjiang Uygur, Peoples R China
[3] Med Univ Xinjiang, Dept Pathol, Urumqi 830054, Xinjiang Uygur, Peoples R China
[4] Xinjiang Med Univ, Clin Med Res Inst, Affiliated Hosp 1, Urumqi 830054, Xinjiang Uygur, Peoples R China
[5] Xinjiang Med Univ, Dept Uyghur Med, Urumqi 830054, Xinjiang Uygur, Peoples R China
关键词
ring finger protein 113A; prognosis; esophageal squamous cell carcinoma; migration; invasion; proliferation; RING FINGER PROTEIN; UBIQUITIN E3 LIGASE; MESENCHYMAL TRANSITION; CANCER; EXPRESSION; GENE; METASTASIS; IDENTIFICATION; PROGRESSION; PROTEASOME;
D O I
10.3892/ijo.2018.4253
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ring finger protein 113A (RNF113A) possesses a C3HC4 zinc finger domain and this domain is found in E3 ubiquitin ligase and is involved in tumorigenesis. To date, and at least to the best of our knowledge, there are no studies available which have investigated RNF113A in cancer. Thus, this study aimed to explore the role of RNF113A in the development of esophageal squamous cell carcinoma (ESCC). For this purpose, paraffin-embedded samples from 117 patients with ESCC were selected, as well as 41 pairs of fresh-frozen ESCC and adjacent normal tissue samples. RNF113A expression was examined by immunohistochemistry and reverse transcription-quantitative PCR (RT-qPCR). RNF113A was overexpressed or silenced in the EC9706 and Eca109 cells. The cells were examined for cell cycle progression, apoptosis, invasiveness and migration. Xenograft tumors were also created in mice using the Eca109 cells. Tumor differentiation (P=0.008) and T classification (P<0.001) were found to be significantly associated with RNF113A expression. No statistically significant association was observed between RNF113A expression and sex, age, histological type, tumor location and lymph node metastasis (N classification). Kaplan-Meier analysis revealed that the patients with ESCC with ahigh expression of RNF113A had a lower survival rate than those with a low expression (P=0.002). Multivariate analysis revealed that RNF113A expression (HR=2.406; 95% CI, 1.301-4.449, P=0.005) was independently associated with overall survival in patients with ESCC. The overexpression of RNF113A promoted proliferation, migration, and invasiveness of ESCC cell lines in vitro, and RNF113A silencing reversed these malignant behaviors. RNF113A knockdown inhibited tumor growth in vivo. Thus, these results indicate that RNF113A promotes the proliferation, migration and invasiveness of ESCC cell lines. RNF113A expression in ESCC is this associated with a poor prognosis of affected patients.
引用
收藏
页码:861 / 871
页数:11
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