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10.1186/s13018-017-0599-7

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suck abstract from ncbi


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pmid28679390
      J+Orthop+Surg+Res 2017 ; 12 (1 ): 103
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  • LncRNA-ANCR regulates the cell growth of osteosarcoma by interacting with EZH2 and affecting the expression of p21 and p27 #MMPMID28679390
  • Zhang F ; Peng H
  • J Orthop Surg Res 2017[Jul]; 12 (1 ): 103 PMID28679390 show ga
  • BACKGROUND: Osteosarcoma (OS) is one of the most common malignant tumors developed in the bone. EZH2 has been found to play pivotal roles in the development of various cancers. LncRNA-ANCR (anti-differentiation ncRNA) has been reported to interact with EZH2 and regulated osteoblast differentiation. Our study aimed to investigate the effect of lncRNA-ANCR on the tumorigenesis of osteosarcoma and explore the underlying molecular mechanism. METHODS: RT-PCR was performed to detect the messenger RNA (mRNA) levels of lncRNA-ANCR, EZH2, p21, and p27 in OS tissues and cell lines. The cell proliferation, transwell invasion, and migration assays were conducted to evaluate the influence of lncRNA-ANCR depletion on the growth of OS cells. RNA pull-down assay was carried out to detect the interaction between lncRNA-ANCR and EZH2. Correlation between the expression of lncRNA-ANCR and the expression of EZH2 were analyzed by cross-tabulation. RESULTS: LncRNA-ANCR is highly expressed in both OS tissues and cell lines. Reduced expression of lncRNA-ANCR inhibited the cell proliferation, invasion, and migration of OS cells. The cell apoptosis rate was also increased with the overexpression of lncRNA-ANCR. Mechanistically, downregulation of lncRNA-ANCR reduced the mRNA level of EZH2 and increased the expression of p21 and p27 at both mRNA and protein levels. LncRNA-ANCR interacted with EZH2 and their expression abundance was positively correlated in OS patients. CONCLUSION: LncRNA-ANCR inhibited the cell proliferation, migration, and invasion of OS cells possibly through interacting with EZH2 and regulating the expression of p21 and p27.
  • |Cell Line, Tumor [MESH]
  • |Cyclin-Dependent Kinase Inhibitor p27/*metabolism [MESH]
  • |Enhancer of Zeste Homolog 2 Protein/*metabolism [MESH]
  • |Humans [MESH]
  • |Osteosarcoma/*enzymology [MESH]
  • |RNA, Long Noncoding/*metabolism [MESH]


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