scholarly journals Long non-coding RNA PCAT1 facilitates cell growth in multiple myeloma through an MTDH-mediated AKT/β-catenin signaling pathway by sponging miR-363-3p

RSC Advances ◽  
2019 ◽  
Vol 9 (58) ◽  
pp. 33834-33842
Author(s):  
Ying Chen ◽  
Jinxia Hao ◽  
Jing Zhao ◽  
Ye Liu ◽  
Yuan Li ◽  
...  

Multiple Myeloma (MM) is a plasma cell myeloma.

RSC Advances ◽  
2021 ◽  
Vol 11 (11) ◽  
pp. 6246-6246
Author(s):  
Laura Fisher

Retraction of ‘Long non-coding RNA PCAT1 facilitates cell growth in multiple myeloma through an MTDH-mediated AKT/β-catenin signaling pathway by sponging miR-363-3p’ by Ying Chen et al., RSC Adv., 2019, 9, 33834–33842, DOI: 10.1039/C9RA06188F.


2020 ◽  
Vol 15 (1) ◽  
pp. 284-295
Author(s):  
Yongtian Zhang ◽  
Dandan Zhao ◽  
Shumei Li ◽  
Meng Xiao ◽  
Hongjing Zhou ◽  
...  

AbstractMultiple myeloma (MM) is a serious health issue in hematological malignancies. Long non-coding RNA taurine-upregulated gene 1 (TUG1) has been reported to be highly expressed in the plasma of MM patients. However, the functions of TUG1 in MM tumorigenesis along with related molecular basis are still undefined. In this study, increased TUG1 and decreased microRNA-34a-5p (miR-34a-5p) levels in MM tissues and cells were measured by the real-time quantitative polymerase reaction assay. The expression of relative proteins was determined by the Western blot assay. TUG1 knockdown suppressed cell viability, induced cell cycle arrest and cell apoptosis in MM cells, as shown by Cell Counting Kit-8 and flow cytometry assays. Bioinformatics analysis, luciferase reporter assay, and RNA pull-down assay indicated that miR-34a-5p was a target of TUG1 and directly bound to notch receptor 1 (NOTCH1), and TUG1 regulated the NOTCH1 expression by targeting miR-34a-5p. The functions of miR-34a-5p were abrogated by TUG1 upregulation. Moreover, TUG1 loss impeded MM xenograft tumor growth in vivo by upregulating miR-34a-5p and downregulating NOTCH1. Furthermore, TUG1 depletion inhibited the expression of Hes-1, Survivin, and Bcl-2 protein in MM cells and xenograft tumors. TUG1 knockdown inhibited MM tumorigenesis by regulating the miR-34a-5p/NOTCH1 signaling pathway in vitro and in vivo, deepening our understanding of the TUG1 function in MM.


Oncotarget ◽  
2017 ◽  
Vol 8 (55) ◽  
pp. 94554-94568 ◽  
Author(s):  
Yangyang Hu ◽  
Chao Deng ◽  
He Zhang ◽  
Jing Zhang ◽  
Bo Peng ◽  
...  

2017 ◽  
Vol 7 (1) ◽  
Author(s):  
Yuanyuan Sun ◽  
Jing Pan ◽  
Ning Zhang ◽  
Wei Wei ◽  
Shanshan Yu ◽  
...  

2018 ◽  
Vol 103 ◽  
pp. 1727-1732 ◽  
Author(s):  
Qian-yu Li ◽  
Li Chen ◽  
Ning Hu ◽  
Hongmian Zhao

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