Abstract | OBJECTIVE: PATIENTS AND METHODS: DLEU1 expression level in ccRCC tissues and para-cancerous tissues was determined by quantitative Real Time-Polymerase Chain Reaction (qRT-PCR). The correlation between DLEU1 expression and pathological indexes of ccRCC patients was assessed. After the silence of DLUE1, the proliferative and migratory abilities of ACHN and 786-O cells were evaluated. Furthermore, Dual- Luciferase reporter gene assay and rescue experiments were conducted to identify the role of DLEU1/ miRNA-194-5p in regulating the ccRCC progression in vitro. RESULTS: DLEU1 expression was markedly up-regulated in ccRCC tissues when compared with para-cancerous tissues. The rates of lymphatic metastasis and distant metastasis in ccRCC patients with a high level of DLEU1 were significantly higher, whereas the prognosis was significantly worse. Transfection of si-DLEU1 remarkably attenuated proliferative and migratory abilities of ACHN and 786-O cells. MiRNA-194-5p was identified as the target gene of DLEU1. In addition, the knockdown of miRNA-194-5p could reverse the regulatory effect of DLEU1 on the proliferative and metastatic abilities of ccRCC. CONCLUSIONS: DLEU1 is closely related to lymphatic metastasis, distant metastasis, and poor prognosis of ccRCC. It aggravates the progression of ccRCC by targeting miRNA-194-5p.
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Authors | G-Z He, S-Y Yu, Q-P Zhou, M-L Chen, Y-W Zhang, Y Zheng, Z-B Zhang, Z-Y Han, J Yu |
Journal | European review for medical and pharmacological sciences
(Eur Rev Med Pharmacol Sci)
Vol. 23
Issue 24
Pg. 10691-10698
(Dec 2019)
ISSN: 2284-0729 [Electronic] Italy |
PMID | 31858537
(Publication Type: Journal Article, Retracted Publication)
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Chemical References |
- DLEU1 lncRNA, human
- MIRN194 microRNA, human
- MicroRNAs
- RNA, Long Noncoding
- Tumor Suppressor Proteins
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Topics |
- Aged
- Carcinoma, Renal Cell
(genetics, pathology)
- Cell Line, Tumor
- Cell Movement
(genetics)
- Cell Proliferation
(genetics)
- Female
- Gene Silencing
- Humans
- Kidney Neoplasms
(genetics, pathology)
- Male
- MicroRNAs
(genetics)
- Middle Aged
- Prognosis
- RNA, Long Noncoding
(genetics)
- Transfection
- Tumor Suppressor Proteins
(genetics)
- Up-Regulation
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