Lentiviral-mediated overexpression of KCTD12 inhibits the proliferation of human uveal melanoma OCM-1 cells

被引:14
作者
Luo, Lifu [1 ,2 ]
Cui, Jizhe [1 ]
Feng, Zhitong [2 ]
Li, Yana [2 ]
Wang, Mengdi [1 ]
Cai, Yong [2 ,3 ,4 ]
Wu, Yazhen [1 ]
Jin, Jingji [2 ,3 ,4 ]
机构
[1] Jilin Univ, Hosp 2, Dept Ophthalmol, Changchun 130041, Jilin, Peoples R China
[2] Jilin Univ, Sch Life Sci, Changchun 130012, Jilin, Peoples R China
[3] Jilin Univ, Natl Engn Lab AIDS Vaccine, Changchun 130012, Jilin, Peoples R China
[4] Jilin Univ, Chinese Minist Educ, Key Lab Mol Enzymol & Engn, Changchun 130012, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
KCTD12; OCM-1; uveal melanoma; xenograft growth; proliferation; EPITHELIAL-MESENCHYMAL TRANSITION; GABA(B) RECEPTORS; METHYLATION; DIAGNOSIS; BIOMARKER; PFETIN; FAMILY; GENE;
D O I
10.3892/or.2016.5325
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human potassium channel tetramerization domain containing 12 (KCTD12, also known as Pfetin) is a member of the KCTD family which consists of 26 members. It has been reported that KCTD12 regulates agonist potency and kinetics of GABA(B) receptor signaling. Proteomic analysis indicates that KCTD12 may be a potential biomarker for the diagnosis and prognosis of gastrointestinal stromal tumors. However, little has been reported concerning the role of KCTD12 in the other tumor types. In the present study, we designed and subcloned N-terminally Flag-tagged human KCTD12 into the pLVX-Puro vector. We then generated a human uveal melanoma cell line (OCM-1) stably expressing KCTD12. Using this stable cell line, we performed a series of experiments including colony formation, invasion, migration and wound healing assays, flow cytometry and western blotting. Based on the experimental results, we first demonstrated that KCTD12 effectively suppressed the proliferation of OCM-1 cells and limited the spread of OCM-1 cells. In the flow cytometric analysis, prolongation of the progression of G2/M to G1 phase in the KCTD12-overexpressing OCM-1 cells was observed. In addition, inhibition of KCTD12-overexpressing OCM-1 cell xenograft growth in nude mice was observed. Taken together, KCTD12 may serve as a novel therapeutic target for patients with uveal melanoma.
引用
收藏
页码:871 / 878
页数:8
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