LncRNA MT1JP acts as a tumor inhibitor via reciprocally regulating Wnt/β-Catenin pathway in retinoblastoma

被引:3
|
作者
Bi, L. -L. [1 ]
Han, F. [2 ]
Zhang, X. -M. [3 ]
Li, Y. -Y. [2 ]
机构
[1] Mudanjiang Coll Med, Affiliated Hosp 2, Dept Med Engn, Mudanjiang, Peoples R China
[2] Mudanjiang Coll Med, Affiliated Hosp 2, Dept Ophthalmol, Mudanjiang, Peoples R China
[3] Mudanjiang Coll Med, Dept Lib, Mudanjiang, Peoples R China
关键词
Retinoblastoma; MT1JP; beta-catenn signaling; EMT; LONG NONCODING RNAS; HUMAN BREAST-CANCER; CELL LUNG-CANCER; SIGNALING PATHWAY; INTRAARTERIAL CHEMOTHERAPY; CERVICAL-CANCER; PROLIFERATION; METASTASIS; INVASION; ADENOCARCINOMA;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
OBJECTIVE: The aim of this study was to investigate the roles of MT1JP and beta-catenin in retinoblastoma. PATIENTS AND METHODS: We performed quantitative Reverse Transcriptase-Polymerase Chain Reaction (qRT-PCR) to quantify the expressions of MT1JP and beta-catenin in 44 retinoblastoma tissues and matched non-tumor tissues. What's more. retinoblastoma cell lines were transfected with pcDNA3.1-MT1JP, after which proliferation, cell cycle, apoptosis, and expression of beta-catenin as well as its downstream targets were assayed. We also conducted TOP-Flash reporter assay to explore the activity of Wnt/beta-catenin signaling pathway. RESULTS: The results revealed that MT1JP was down-regulated, while beta-catenin was highly expressed in retinoblastoma cells. Meanwhile, the forced expression of MT1JP impaired the expression of the beta-catenin protein and its downstream targets such as cyclin D1. c-myc. CONCLUSIONS: We demonstrated that MT1JP was a tumor suppressor by negatively modulating the activity of the Wnt/beta-catenin signaling pathway in the development of retinoblastoma and might function as a prognostic biomarker and therapeutic target.
引用
收藏
页码:4204 / 4214
页数:11
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